Conditions » Condition

Menopause

Menopause is a natural biological transition marking the end of reproductive years, occurring when the ovaries stop producing estrogen and progesterone. While universal among women, menopause affects each woman differently — some experience minimal symptoms while others face years of hot flashes, sleep disruption, mood changes, and metabolic shifts increasing cardiovascular disease and osteoporosis risk. Understanding menopause stages, recognizing symptoms, knowing treatment options, and implementing preventive strategies enables women to navigate this transition while protecting long-term health.

Menopause is a natural biological process marking the permanent end of menstruation and reproductive capacity. It occurs when the ovaries stop producing estrogen and progesterone, the hormones regulating the menstrual cycle and supporting numerous body systems. While menopause is universal among women — every woman who lives long enough will experience it — the transition’s impact varies dramatically. Some women sail through with minimal symptoms, while others endure years of severe hot flashes, night sweats, sleep disruption, mood changes, and physical discomfort significantly affecting quality of life.

The average age of menopause in the United States is 51, but the transition typically begins several years earlier during perimenopause, when hormone levels fluctuate erratically causing irregular periods and emerging symptoms. This perimenopausal phase, lasting 4-8 years on average, is often the most symptomatic period, with women experiencing unpredictable hormonal swings creating a constellation of physical and psychological symptoms.

Beyond immediate symptoms, menopause triggers fundamental physiological changes affecting multiple body systems. The decline in estrogen — which previously protected cardiovascular health, bone density, metabolism, brain function, and urogenital tissues—increases risk for heart disease, stroke, osteoporosis, weight gain, diabetes, cognitive changes, and urinary problems. These long-term health implications make menopause not just a symptomatic transition but a critical health inflection point requiring proactive management.

What makes menopause particularly challenging is that it remains underrecognized and undertreated. Many women endure years of symptoms without realizing they’re menopausal. Healthcare providers may not inquire about symptoms or offer treatment options. Stigma and misinformation prevent women from seeking help. The result is unnecessary suffering and missed opportunities for symptom relief and health protection.

Understanding menopause — its stages, symptoms, hormonal changes, treatment options, and long-term health implications—empowers women to navigate this transition effectively. Armed with knowledge, women can recognize symptoms early, access appropriate treatment, make informed decisions about hormone therapy and other interventions, implement preventive strategies, and advocate for the care they deserve during this significant life phase.

Quick Summary:


What Is Menopause?

Menopause is defined as the point in time when menstrual periods have stopped permanently, marking the end of the reproductive years. Specifically, menopause is confirmed when a woman has gone 12 consecutive months without a menstrual period, with no other obvious cause (pregnancy, certain medications, or medical conditions affecting menstruation).

This definition is retrospective—you can only confirm menopause has occurred after a full year without periods. During perimenopause, periods may stop for months then resume, creating uncertainty about whether menopause has truly begun. The 12-month rule exists because ovarian function can be erratic during the transition, with occasional ovulation occurring even after prolonged amenorrhea (absence of periods).

The Biology of Menopause

Menopause occurs because the ovaries, which contain a finite number of eggs (follicles), gradually deplete their supply over a woman’s lifetime. From birth, a female has approximately 1-2 million follicles. By puberty, about 300,000 remain. During each menstrual cycle, a cohort of follicles begins maturing, though typically only one releases an egg (ovulation) while others degenerate. This continuous follicle loss accelerates with age.

As follicle numbers decline, the ovaries become progressively less responsive to the pituitary hormones (follicle-stimulating hormone or FSH, and luteinizing hormone or LH) that normally stimulate follicle maturation and ovulation. The remaining follicles require higher FSH levels to respond, causing FSH to rise—a key hormonal marker of approaching menopause.

Simultaneously, the ovaries produce less estrogen and progesterone. Estrogen levels fluctuate wildly during perimenopause—sometimes very high when multiple follicles develop, sometimes very low when ovulation fails. Eventually, estrogen production drops to consistently low levels as follicles are exhausted. Progesterone, produced by the corpus luteum after ovulation, declines as ovulation becomes infrequent and finally ceases.

The loss of estrogen and progesterone affects far more than reproduction. Estrogen receptors exist throughout the body—in the brain, cardiovascular system, bones, skin, urogenital tissues, and metabolic organs. The hormone decline therefore triggers widespread physiological changes, explaining menopause’s diverse symptoms and health impacts.

Natural vs. Surgical vs. Medical Menopause

Natural Menopause:

Occurs spontaneously due to age-related ovarian follicle depletion, typically between ages 45-55. This is the universal female experience for those who don’t undergo surgical or medical interventions causing premature menopause.

Surgical Menopause:

Results from bilateral oophorectomy (removal of both ovaries). When ovaries are removed, menopause occurs immediately regardless of age, as the body loses its primary estrogen source. Women who undergo hysterectomy (uterus removal) without oophorectomy continue producing hormones and experience natural menopause timing, though they can’t use menstrual cessation as a marker.

Surgical menopause is often more symptomatic than natural menopause because hormone levels drop abruptly rather than gradually declining over years. The sudden estrogen loss can cause severe hot flashes, mood changes, and other symptoms. Surgical menopause before natural menopause age significantly increases cardiovascular and bone disease risks unless hormone therapy is provided.

Medical Menopause:

Can be induced by chemotherapy, radiation therapy, or medications that suppress ovarian function. Chemotherapy and radiation, particularly when treating cancers, can damage ovarian follicles causing temporary or permanent menopause depending on age, treatment type, and dosage. Younger women may recover ovarian function after treatment, while older women near natural menopause age more commonly experience permanent menopause.

Certain medications deliberately induce temporary medical menopause for treating conditions like endometriosis or fibroids. GnRH agonists (leuprolide, goserelin) suppress pituitary hormone release, shutting down ovarian function. When medication stops, ovarian function typically resumes.

Age and Timing

The average age of natural menopause in the United States and most developed countries is 51 years, with normal range considered 45-55 years. Genetics strongly influences timing—women typically experience menopause within a few years of their mother’s age at menopause.

Factors associated with earlier menopause:

Factors associated with later menopause:

Early or Premature Menopause:

Menopause before age 40 is considered premature (also called premature ovarian insufficiency or POI). This affects approximately 1% of women. Between ages 40-45 is considered early menopause, affecting about 5% of women. Both premature and early menopause significantly increase long-term health risks including cardiovascular disease, osteoporosis, cognitive decline, and mortality, primarily because women miss years of estrogen’s protective effects. Hormone therapy is typically strongly recommended until at least age 50-51 (average natural menopause age) to mitigate these risks.


The Stages of Menopause

Menopause is not a single event but a process unfolding over years. Understanding the stages helps women recognize where they are in the transition and what to expect.

Reproductive Years

The reproductive years span from menarche (first period) through the late 30s or early 40s. During this time, menstrual cycles are generally regular, ovulation occurs reliably, and hormone levels remain relatively stable. Fertility gradually declines starting in the early 30s, accelerating after age 35, but pregnancy remains possible throughout this period.

Perimenopause (Menopausal Transition)

Perimenopause is the transition phase leading to menopause, lasting on average 4-8 years but ranging from a few months to over a decade. It typically begins in the mid-to-late 40s but can start in the late 30s or early 40s for some women.

Early Perimenopause:

Characterized by variable cycle length—periods may come closer together or further apart by 7 days or more compared to normal cycle length. Menstrual flow may become heavier or lighter. Hormone levels, particularly estrogen, fluctuate widely from cycle to cycle and even within a single cycle. Some women begin experiencing symptoms like hot flashes, sleep disruption, or mood changes during early perimenopause, though many remain asymptomatic.

FSH levels begin rising as the ovaries require more stimulation to release eggs, though FSH remains variable—sometimes elevated, sometimes normal—making it an unreliable diagnostic marker during perimenopause.

Late Perimenopause:

Marked by increasing menstrual irregularity with skipped periods. Two or more missed cycles in a row, or amenorrhea lasting 60 days or more, signals entry into late perimenopause. Cycles become increasingly unpredictable. Some women experience very long cycles (90+ days) alternating with short cycles. Menstrual flow can be extremely heavy (flooding) or very light.

Symptoms typically intensify during late perimenopause as estrogen levels drop more consistently low. Hot flashes, night sweats, sleep disruption, mood changes, and other symptoms often peak during this phase. Many women find late perimenopause the most challenging period symptomatically.

Pregnancy remains possible throughout perimenopause, though fertility declines substantially. Contraception is recommended until 12 months after the final period for women over 50, or 24 months for women under 50.

Menopause

Menopause itself is the point in time 12 months after the final menstrual period. It’s a single moment marking the transition from perimenopause to postmenopause. Some women experience symptom relief around this time as hormone levels stabilize at consistently low levels, though many continue experiencing symptoms for years.

Postmenopause

Postmenopause encompasses all years following menopause—from 12 months after the final period until end of life. Early postmenopause (first 5-10 years) is when bone loss is most rapid and cardiovascular risk increases most dramatically. Symptoms like hot flashes, night sweats, and sleep disruption gradually improve for most women, though 10-15% continue experiencing symptoms for many years or even decades.

Long-term effects of estrogen deficiency—urogenital atrophy, skin changes, ongoing increased cardiovascular and bone disease risk—persist throughout postmenopause. This phase represents potentially 30-40 years of life, emphasizing the importance of health management after menopause.


Common Symptoms of Menopause

Menopause symptoms result from declining estrogen and progesterone levels affecting multiple body systems. Symptoms typically begin during perimenopause, often peak during late perimenopause and early postmenopause, and gradually improve over time, though some women experience symptoms for decades.

Symptom severity varies dramatically among women. Approximately 20-30% of women experience minimal symptoms requiring no treatment. About 40-50% have moderate symptoms that are bothersome but manageable. Another 20-30% suffer severe, disruptive symptoms significantly impairing quality of life, work performance, and relationships. This variability explains why some women describe menopause as a non-issue while others find it profoundly debilitating.

Vasomotor Symptoms (Hot Flashes and Night Sweats)

Vasomotor symptoms—hot flashes (also called hot flushes) and night sweats—are the hallmark menopausal symptoms, affecting approximately 75% of women. A hot flash is a sudden sensation of intense heat spreading through the upper body and face, often accompanied by flushing (skin redness), rapid heartbeat, and sweating. Hot flashes typically last 1-5 minutes but can persist for 30 minutes or longer. Night sweats are hot flashes occurring during sleep, often drenching sleepwear and bedding, causing sleep disruption.

Hot flashes result from estrogen withdrawal affecting the hypothalamus, the brain region regulating body temperature. Declining estrogen narrows the thermoneutral zone—the temperature range in which the body maintains core temperature without triggering warming or cooling mechanisms. With a narrow thermoneutral zone, small temperature fluctuations trigger inappropriate heat dissipation responses (sweating, vasodilation) producing the hot flash sensation.

Frequency and Duration:

Hot flash frequency varies from occasional (a few per week) to very frequent (30+ per day). Average frequency is 7-10 per day during peak symptomatic years. For most women, hot flashes occur for 4-5 years, though median duration is 7-9 years and 10-15% of women experience hot flashes for decades. Severe, frequent, long-lasting hot flashes are more common in African American women, smokers, women with higher BMI, and those who experienced early menopause.

Impact:

Moderate to severe hot flashes significantly impair quality of life. Sleep disruption from night sweats causes fatigue, mood changes, difficulty concentrating, and reduced daytime functioning. Frequent daytime hot flashes cause embarrassment, discomfort, and interference with work and social activities. Severe vasomotor symptoms are strongly associated with depression, anxiety, and reduced work productivity.

Sleep Disturbances

Sleep problems affect 40-60% of menopausal women. While night sweats are an obvious cause of sleep disruption, many women experience insomnia independent of hot flashes. Difficulty falling asleep, frequent nighttime awakenings, early morning awakening, and non-restorative sleep are all common. Estrogen and progesterone both influence sleep regulation, and their decline disrupts sleep architecture, reduces deep sleep, and increases sleep fragmentation.

Poor sleep creates a cascade of secondary problems: daytime fatigue, irritability, mood changes, difficulty concentrating, reduced stress resilience, and impaired immune function. Chronic sleep deprivation worsens hot flashes, creating a vicious cycle. Sleep disturbance is one of the most distressing menopausal symptoms because it affects all aspects of daily functioning.

Mood Changes and Psychological Symptoms

Many women experience mood changes during perimenopause and early postmenopause, including irritability, mood swings, anxiety, and depression. The risk of first-time major depression doubles during perimenopause compared to premenopausal years. Irritability—finding small annoyances disproportionately frustrating—is particularly common and often distressing to women who previously felt emotionally stable.

Estrogen influences neurotransmitter systems including serotonin, dopamine, and norepinephrine, all involved in mood regulation. Estrogen fluctuations during perimenopause may trigger mood symptoms in susceptible women. Additionally, the stress of managing menopausal symptoms, sleep deprivation, life stressors common in middle age (aging parents, teenage children, career pressures), and cultural attitudes about aging all contribute to psychological symptoms.

It’s important to distinguish primary mood disorders (major depression, anxiety disorders) from menopause-related mood changes. Women with history of depression, premenstrual syndrome (PMS), or postpartum depression are at higher risk for perimenopausal mood symptoms. Persistent depressed mood, loss of interest in activities, hopelessness, or suicidal thoughts require evaluation and treatment by mental health professionals, not just menopause management.

Cognitive Changes

Many women report “brain fog,” difficulty concentrating, forgetfulness, word-finding difficulties, and reduced mental sharpness during perimenopause. Memory complaints are common, particularly difficulty remembering names or where items were placed. These cognitive changes can be frustrating and concerning, raising fears about dementia.

Research confirms that some women experience measurable cognitive changes during perimenopause, particularly in verbal memory and processing speed. However, these changes are typically subtle and don’t interfere significantly with daily functioning for most women. Importantly, perimenopause-related cognitive changes appear temporary—cognitive function generally returns to baseline in postmenopause.

Estrogen influences brain function, particularly in regions involved in memory and attention. The hormone fluctuations and ultimate decline during perimenopause may temporarily affect cognitive performance. Sleep deprivation, mood symptoms, and stress all independently impair cognition, likely contributing to perimenopausal brain fog.

While perimenopause-related cognitive changes don’t increase dementia risk, it’s important to distinguish normal menopausal cognitive changes from pathological cognitive decline. Progressive, worsening memory problems, difficulty with familiar tasks, getting lost in familiar places, personality changes, or inability to manage daily activities require medical evaluation.

Vaginal and Urogenital Changes

Estrogen maintains the health of vaginal and urogenital tissues. Without estrogen, these tissues undergo atrophy—becoming thinner, drier, less elastic, and more fragile. This genitourinary syndrome of menopause (GSM), previously called vulvovaginal atrophy, affects 50-70% of postmenopausal women but is often underreported due to embarrassment.

Vaginal Symptoms:

Urinary Symptoms:

Unlike hot flashes which often improve with time, urogenital symptoms typically worsen progressively without treatment because tissues continue atrophying as estrogen remains deficient. These symptoms significantly impact sexual function, intimate relationships, and quality of life. The good news is that urogenital symptoms respond well to treatment, particularly vaginal estrogen therapy.

Sexual Function Changes

Sexual changes during and after menopause are multifactorial. Vaginal dryness and painful intercourse directly impair sexual activity. Decreased libido (sexual desire) affects many menopausal women due to declining testosterone (produced by ovaries and adrenal glands), estrogen deficiency, mood changes, fatigue, body image concerns, and relationship factors. Difficulty with arousal and achieving orgasm may occur. The time required for arousal typically increases, and genital sensitivity may decrease.

It’s important to recognize that menopausal hormone changes affect sexual function, but psychological, relationship, and sociocultural factors are equally important. Women in satisfying relationships with partners they find attractive, who prioritize sexual intimacy, who maintain positive attitudes about sexuality, and who address physical symptoms are more likely to maintain sexual satisfaction despite hormonal changes.

Weight Gain and Body Composition Changes

Weight gain averaging 5-10 pounds is common during the menopausal transition, though not inevitable. More significant than weight gain is body composition change—fat redistributes from hips and thighs to the abdomen, creating an “apple” rather than “pear” body shape. This visceral (abdominal) fat accumulation increases cardiovascular and metabolic disease risk.

Multiple factors contribute to menopausal weight gain:

Weight management becomes more challenging during menopause, requiring dietary adjustments, increased physical activity, particularly resistance training to preserve muscle mass, and addressing sleep and stress.

Joint and Muscle Pain

Joint pain, stiffness, and muscle aches affect 50-60% of menopausal women. Hands, knees, hips, and neck are commonly affected. Pain and stiffness may be worse in the morning. Estrogen has anti-inflammatory effects and influences joint and connective tissue health; its decline may contribute to musculoskeletal symptoms. Some women develop new onset arthritis during perimenopause, though whether menopause causes arthritis or simply coincides with age-related arthritis development remains debated.

Other Physical Symptoms

Headaches: Migraine headaches often worsen during perimenopause due to estrogen fluctuations, though typically improve after menopause when hormone levels stabilize.

Heart Palpitations: Sudden awareness of heartbeat—feeling the heart racing, pounding, or skipping beats—affects some women during perimenopause. Palpitations are usually benign but should be evaluated to rule out cardiac arrhythmias.

Dizziness: Light-headedness or spinning sensations (vertigo) can occur, often associated with hot flashes.

Dry Skin and Hair Changes: Skin becomes drier, thinner, less elastic, and more prone to wrinkles. Hair may thin, become drier, or change texture.

Breast Changes: Breasts may become less firm, change shape, or feel tender.


Hormone Changes During Menopause

Understanding the hormonal changes underlying menopause clarifies why symptoms occur and how treatments work.

Estrogen

Estrogen (primarily estradiol, abbreviated E2) is the primary female sex hormone, produced mainly by developing ovarian follicles. Estrogen orchestrates the menstrual cycle, maintains reproductive tissues, and influences numerous body systems including cardiovascular, skeletal, central nervous, urogenital, and skin.

During perimenopause, estrogen levels fluctuate unpredictably—sometimes very high when multiple follicles develop, sometimes very low when ovulation fails. These erratic swings cause many perimenopausal symptoms. Eventually, as follicles are exhausted, estrogen production drops to consistently low levels.

Postmenopausal estrogen levels are approximately 90% lower than premenopausal levels. The ovaries produce minimal estrogen after menopause. Most remaining estrogen comes from conversion of androgens (testosterone, androstenedione) to estrone (E1, a weaker estrogen) in fat tissue and other peripheral sites. This peripheral conversion explains why higher body weight is associated with slightly higher postmenopausal estrogen levels.

Progesterone

Progesterone is produced by the corpus luteum (the follicle remnant after ovulation). Its primary role is preparing the uterine lining for pregnancy and maintaining early pregnancy. Progesterone opposes estrogen’s effects on the uterine lining, preventing excessive growth.

During perimenopause, as ovulation becomes infrequent, progesterone production becomes erratic and eventually ceases. By menopause, progesterone levels are near zero. The loss of progesterone’s calming effects on the central nervous system may contribute to sleep disturbances, anxiety, and mood changes.

Testosterone and Other Androgens

Though often considered male hormones, androgens including testosterone are important for female sexual desire, energy, muscle and bone health. The ovaries and adrenal glands produce testosterone and other androgens (DHEA, androstenedione).

Testosterone levels decline gradually with age starting in the 20s, accelerating after menopause. However, the relative decline is less dramatic than estrogen’s drop. Some postmenopausal women maintain adequate testosterone levels while others become relatively androgen deficient, potentially contributing to decreased libido, fatigue, and reduced sense of well-being.

Follicle-Stimulating Hormone (FSH) and Luteinizing Hormone (LH)

FSH and LH are pituitary hormones that stimulate the ovaries. As ovarian follicles decline and become less responsive, the pituitary compensates by producing more FSH and LH. Rising FSH is the most consistent hormonal marker of approaching menopause.

In perimenopause, FSH levels are elevated but fluctuate considerably—sometimes very high, sometimes normal—depending on remaining ovarian function. In postmenopause, FSH remains consistently elevated (typically >25-30 IU/L). Measuring FSH can help confirm menopause in women over 45 who have stopped having periods, though it’s not always necessary since menopause is primarily a clinical diagnosis based on age and cessation of menstruation.


Diagnosis of Menopause

Menopause is primarily a clinical diagnosis based on age and menstrual history. For women over age 45 experiencing irregular periods and menopausal symptoms, no laboratory testing is required to diagnose menopause or perimenopause. The diagnosis is made by recognizing the classic symptom pattern in the appropriate age range.

When Is Testing Indicated?

Testing is typically recommended when:

Testing is generally not needed when:

Hormone Testing

A number of blood tests are associated with menopause identification.

FSH (Follicle-Stimulating Hormone):

FSH >25-30 IU/L suggests menopause or perimenopause, especially if accompanied by low estradiol. However, FSH fluctuates during perimenopause, so a single normal FSH doesn’t exclude perimenopause. FSH testing is most useful for diagnosing premature or early menopause in younger women.

Estradiol:

Low estradiol (<20-30 pg/mL) combined with elevated FSH suggests menopause. Estradiol also fluctuates during perimenopause, limiting diagnostic utility.

AMH (Anti-Müllerian Hormone):

AMH reflects remaining ovarian follicle reserve. Very low or undetectable AMH suggests diminished ovarian reserve and approaching menopause. AMH is more stable than FSH or estradiol but is expensive and not widely used for menopause diagnosis.

Testosterone, DHEA-S:

May be measured if androgen deficiency is suspected (severe fatigue, low libido despite addressing other factors).

TSH (Thyroid-Stimulating Hormone):

Thyroid disorders are common in middle-aged women and can cause symptoms mimicking menopause (fatigue, mood changes, weight changes, menstrual irregularities). TSH should be checked if symptoms are atypical or thyroid dysfunction suspected.

Why Hormone Testing During Perimenopause Is Limited

Hormone levels during perimenopause fluctuate dramatically from day to day and even within a single day. A test showing normal FSH and estradiol might show elevated FSH and low estradiol if repeated a week later. This variability means hormone tests can’t reliably diagnose perimenopause or predict timing of final menstrual period. Clinical assessment—age, menstrual pattern changes, and symptoms—is more reliable than laboratory testing for diagnosing perimenopause.


Long-Term Health Effects of Menopause

Beyond immediate symptoms, menopause has profound long-term health implications due to estrogen deficiency’s effects on multiple organ systems. Understanding these health effects emphasizes the importance of proactive health management after menopause.

Cardiovascular Disease

Cardiovascular disease is the leading cause of death in postmenopausal women, and menopause significantly increases cardiovascular risk. Before menopause, women have substantially lower cardiovascular disease rates than age-matched men. After menopause, women’s cardiovascular risk increases rapidly, eventually equaling or exceeding men’s rates.

Estrogen has numerous cardioprotective effects:

The loss of these protective effects explains postmenopausal cardiovascular risk increase. Additionally, menopause is associated with worsening of cardiovascular risk factors: total and LDL cholesterol increase by approximately 10%, HDL cholesterol decreases slightly, triglycerides increase, blood pressure rises, abdominal obesity increases, and insulin resistance worsens. These changes create a perfect storm for accelerated atherosclerosis.

The increase in cardiovascular risk is most dramatic in the first 5-10 years after menopause, emphasizing the importance of aggressive cardiovascular risk factor management during this critical window. Women who experience early menopause (before age 45) have particularly elevated cardiovascular risk because they lose estrogen’s protection years earlier than expected.

Osteoporosis and Bone Health

Bone is dynamic tissue constantly being broken down (resorption) and rebuilt (formation). Estrogen inhibits bone resorption, maintaining the balance between breakdown and rebuilding. When estrogen declines, bone resorption accelerates while formation cannot keep pace, resulting in progressive bone loss.

Bone loss is most rapid in the first 5-7 years after menopause, during which women lose approximately 20% of their bone density. After this accelerated phase, bone loss continues but more slowly. This progressive bone loss increases fracture risk. One in two women over age 50 will experience an osteoporotic fracture in her remaining lifetime. Hip fractures, which have 20% one-year mortality and often result in permanent loss of independence, are particularly devastating.

Risk factors for osteoporosis beyond menopause include:

Bone density testing (DEXA scan) is recommended for all women at age 65, or earlier for women with risk factors. Prevention strategies include adequate calcium and vitamin D, regular weight-bearing and resistance exercise, avoiding smoking and excessive alcohol, and considering bone-protective medications for women at high fracture risk.

Metabolic Changes and Diabetes Risk

Menopause adversely affects metabolism and glucose regulation. Insulin resistance—where cells become less responsive to insulin, requiring higher insulin levels to maintain normal blood glucose—worsens during the menopausal transition. This metabolic shift increases risk for prediabetes, type 2 diabetes, and metabolic syndrome (a cluster of conditions including abdominal obesity, high blood pressure, high blood sugar, and abnormal cholesterol).

The redistribution of body fat to the abdomen (visceral fat accumulation) contributes significantly to insulin resistance and metabolic dysfunction. Visceral fat is metabolically active, releasing inflammatory molecules and fatty acids that impair insulin signaling. The combination of declining estrogen (which influences insulin sensitivity), increasing visceral fat, and age-related changes creates a metabolic perfect storm.

Women with prediabetes or diabetes before menopause often find glucose control becomes more challenging during the transition, requiring medication adjustments. For women without diabetes, menopause represents a critical period for intensifying lifestyle interventions to prevent metabolic disease development.

Cognitive Function and Dementia Risk

The relationship between menopause and long-term cognitive health remains actively researched and incompletely understood. Short-term cognitive changes during perimenopause (brain fog, memory difficulties) appear to resolve in most women. The question is whether menopause affects long-term dementia risk.

Some studies suggest earlier menopause is associated with increased dementia risk, while longer reproductive years (later menopause) may be protective. Women who experience surgical menopause before natural menopause age, particularly if both ovaries are removed before age 45, have increased dementia risk. These findings suggest estrogen may have neuroprotective effects, though this remains controversial.

The timing hypothesis posits that hormone therapy initiated close to menopause may provide cognitive benefits, while hormone therapy started many years after menopause may be harmful. This remains an area of active investigation. What’s clear is that maintaining cardiovascular health, staying physically and mentally active, maintaining social connections, and managing cardiovascular risk factors (which also affect brain health) are important for cognitive health after menopause.

Urogenital Health

Without treatment, genitourinary syndrome of menopause (GSM) worsens progressively after menopause. Vaginal tissues continue atrophying, becoming increasingly thin, dry, fragile, and prone to irritation and infection. Urinary symptoms including urgency, frequency, and recurrent urinary tract infections often develop or worsen. Stress urinary incontinence becomes more common.

These changes significantly impact quality of life, sexual function, and intimate relationships. The good news is that GSM is highly treatable with vaginal estrogen therapy, which restores vaginal tissue health with minimal systemic absorption and excellent safety profile.

Skin and Connective Tissue Changes

Estrogen maintains skin thickness, elasticity, moisture, and collagen content. After menopause, skin thins, becomes drier and less elastic, heals more slowly, and develops more wrinkles. Collagen content decreases by approximately 30% in the first five years after menopause, accelerating thereafter but more slowly. These changes are irreversible and progressive without treatment.


Treatment Options for Menopause

Treatment decisions should be individualized based on symptom severity, health history, personal preferences, and risk-benefit assessment. Not all women require treatment—those with minimal symptoms may choose no intervention. For women with moderate to severe symptoms significantly affecting quality of life, multiple effective treatment options exist.

Hormone Replacement Therapy (HRT)

Hormone replacement therapy, also called menopausal hormone therapy (MHT), is the most effective treatment for menopausal symptoms. HRT involves supplementing the hormones the ovaries no longer produce—estrogen and, for women with a uterus, progesterone (or a progestin).

Types of Hormone Therapy:

Estrogen-only therapy: For women who have had a hysterectomy (uterus removed). Estrogen can be given alone because there’s no uterine lining to protect.

Combined estrogen-progestogen therapy: For women with a uterus. Progestogen (progesterone or synthetic progestin) is added to estrogen to protect the uterine lining from excessive growth (endometrial hyperplasia) that could lead to endometrial cancer. The progestogen can be given continuously (daily) or cyclically (for part of each month).

Estrogen Forms and Routes:

Oral tablets: Conjugated equine estrogens, estradiol, esterified estrogens Transdermal patches: Deliver estradiol through skin Gels, sprays, lotions: Applied to skin Vaginal preparations: Creams, tablets, rings—primarily for urogenital symptoms with minimal systemic absorption

Transdermal estrogen (patches, gels) has advantages over oral estrogen: avoids first-pass liver metabolism, doesn’t increase blood clotting risk, and has more favorable effects on triglycerides and blood pressure.

Progestogen Options:

Micronized progesterone: Bioidentical to natural progesterone, oral Synthetic progestins: Medroxyprogesterone acetate (most studied), norethindrone, and others Levonorgestrel IUD: Releases progestin locally in uterus, providing uterine protection with minimal systemic effects

Benefits of Hormone Therapy:

Risks of Hormone Therapy:

Risks depend on hormone type, dose, duration, route of administration, timing of initiation relative to menopause, and individual factors including age and health history.

Breast Cancer:

Combined estrogen-progestogen therapy slightly increases breast cancer risk with extended use (typically after 3-5 years). The absolute risk increase is small—approximately 1-2 additional breast cancers per 1,000 women using HRT for 5 years. Estrogen-only therapy (in women without a uterus) appears not to increase or may even slightly decrease breast cancer risk.

Cardiovascular Disease:

For healthy women starting HRT near menopause (within 10 years of final period or before age 60), cardiovascular risk is not increased and may even be reduced. However, starting HRT many years after menopause or in women with established cardiovascular disease may increase risk. This “timing hypothesis” explains why HRT effects vary—early initiation in healthy women is safe, while late initiation in older women with atherosclerosis may be harmful.

Blood Clots (Venous Thromboembolism):

Oral estrogen increases blood clot risk approximately 2-fold. Transdermal estrogen does not appear to increase clot risk, making it preferred for women with clotting risk factors. Absolute risk remains low for most women.

Stroke:

Oral estrogen slightly increases stroke risk, particularly in older women starting HRT many years after menopause. For younger, recently menopausal women, stroke risk increase is minimal. Transdermal estrogen appears safer than oral for stroke risk.

Who Should NOT Take Hormone Therapy:

Absolute contraindications (should not use HRT):

Relative contraindications (requires careful assessment):

The Bottom Line on Hormone Therapy:

For healthy women under age 60 or within 10 years of menopause with moderate to severe symptoms, HRT is the most effective treatment with favorable benefit-risk profile. Starting HRT close to menopause and using the lowest effective dose minimizes risks. Estrogen-only therapy for women without a uterus has the most favorable risk profile. Transdermal estrogen is safer than oral regarding blood clots and possibly cardiovascular risk and stroke.

The decision should be individualized, weighing symptom severity, personal risk factors, preferences about treatment type, and ongoing reassessment of benefits and risks. Many women successfully use HRT for 5-10 years or even longer, though the benefits and risks of extended use should be periodically reevaluated.

Non-Hormonal Prescription Medications

For women who cannot or prefer not to use hormone therapy, several non-hormonal medications effectively treat menopausal symptoms, particularly hot flashes.

Selective Serotonin Reuptake Inhibitors (SSRIs) and Serotonin-Norepinephrine Reuptake Inhibitors (SNRIs):

These antidepressants reduce hot flash frequency and severity by 40-60%:

These medications have the dual benefit of treating both hot flashes and mood symptoms if present. Side effects include nausea, headache, insomnia or drowsiness, and sexual dysfunction. Doses used for hot flashes are often lower than antidepressant doses.

Gabapentin (Neurontin):

Originally an anticonvulsant, gabapentin reduces hot flashes by approximately 40-60%. It’s particularly useful for women with sleep problems since it has sedating effects. Typical dose: 300-900 mg daily. Side effects include dizziness, drowsiness, and weight gain.

Fezolinetant (Veozah):

A neurokinin 3 receptor antagonist approved in 2023 specifically for moderate to severe menopausal hot flashes. It reduces hot flash frequency and severity without hormonal effects. Typical dose: 45 mg daily. Side effects include elevated liver enzymes (requiring monitoring), abdominal pain, and back pain. It’s more expensive than other options but provides an effective non-hormonal alternative.

Oxybutynin:

An anticholinergic medication primarily used for overactive bladder, oxybutynin reduces hot flashes by 80% in some studies. Low doses (2.5-5 mg daily) are used for hot flashes. Side effects include dry mouth, constipation, and, rarely, cognitive effects. It’s off-label for hot flashes but gaining acceptance.

Clonidine:

A blood pressure medication that reduces hot flashes modestly (20-40% reduction). Side effects including dry mouth, constipation, drowsiness, and blood pressure lowering limit use.

Vaginal Estrogen Therapy

For women whose primary complaint is urogenital symptoms (vaginal dryness, painful intercourse, urinary symptoms), low-dose vaginal estrogen is highly effective with minimal systemic absorption and excellent safety profile. Vaginal estrogen is appropriate even for women who cannot or prefer not to use systemic HRT.

Forms include:

Vaginal estrogen restores vaginal tissue health, increasing tissue thickness, elasticity, lubrication, and blood flow. It also restores vaginal pH, reducing infection risk. Benefits appear within 2-4 weeks and continue with ongoing use. Because absorption is minimal (blood estradiol levels remain in postmenopausal range), systemic risks including breast cancer and blood clots are not increased. Vaginal estrogen can be used indefinitely as long as beneficial.

Some women use vaginal estrogen in combination with systemic HRT if they need both symptom relief and urogenital treatment.

Lifestyle and Behavioral Interventions

Lifestyle modifications can reduce symptom severity, improve overall health, and mitigate long-term health risks associated with menopause.

For Hot Flashes:

For Sleep:

For Mood:

For Weight Management:

For Bone Health:

For Cardiovascular Health:

For Vaginal Health:

Complementary and Alternative Therapies

Cognitive Behavioral Therapy (CBT):

CBT specifically designed for menopausal symptoms reduces hot flash-related distress, improves mood and sleep, and helps women cope with menopausal transition. It doesn’t reduce hot flash frequency but reduces their impact on quality of life.

Hypnosis:

Clinical hypnotherapy reduces hot flash frequency by approximately 70% in some studies, making it one of the most effective non-pharmacologic interventions.

Acupuncture:

Evidence is mixed, with some studies showing modest hot flash reduction while others show no benefit beyond placebo. Worth considering for women interested in trying non-pharmacologic approaches.

Herbal Supplements:

Many women try herbal supplements for menopausal symptoms:

Black Cohosh: Most studied herbal supplement for menopause. Evidence is mixed regarding effectiveness. Generally well-tolerated but liver toxicity has been reported rarely.

Soy Isoflavones and Red Clover: Contain phytoestrogens (plant compounds with weak estrogen-like effects). Modest benefits in some studies, no benefit in others. Generally safe.

Evening Primrose Oil: No consistent evidence of benefit.

Dong Quai, Ginseng, Wild Yam: No convincing evidence of effectiveness.

Important considerations for herbal supplements:


Prevention and Health Maintenance

Menopause represents a critical opportunity for health assessment and preventive interventions to reduce risks that increase after estrogen decline.

Cardiovascular Disease Prevention

Cardiovascular disease is the leading cause of death in postmenopausal women, making cardiovascular risk reduction the most important health priority. Prevention strategies:

Risk Assessment:

Lifestyle Interventions:

Medical Management:

Osteoporosis Prevention

Bone Density Testing:

DEXA scan at age 65 for all women, or earlier if risk factors present (early menopause, low body weight, fracture history, long-term steroid use, smoking, family history).

Prevention Strategies:

Treatment if Osteoporosis Diagnosed:

Cancer Screening

Breast Cancer:

Mammography every 1-2 years starting at age 40-50 (guidelines vary by organization) continuing as long as life expectancy exceeds 10 years. Women at high risk may need earlier or more frequent screening, possibly with breast MRI.

Cervical Cancer:

Pap smear and/or HPV testing per current guidelines (typically every 3-5 years depending on age and prior results). Many women can discontinue cervical cancer screening after age 65 if prior screening was adequate and no high-risk factors.

Colorectal Cancer:

Screening starting at age 45-50 with colonoscopy every 10 years or alternative screening methods per guidelines.

Lung Cancer:

Low-dose CT screening for current or former heavy smokers ages 50-80.

Metabolic Health

Screening:

Prevention:

Mental Health

Depression and anxiety are common during and after menopause. Regular screening, addressing sleep and symptom management, maintaining social connections, regular exercise, and seeking professional help when needed are all important.


When to See a Healthcare Provider

Women should consult healthcare providers when:

Don’t suffer silently. Effective treatments exist for menopausal symptoms, and proactive health management during this transition protects long-term health.


Living With Menopause

Menopause is a significant life transition, not just physically but psychologically and socially. Cultural attitudes, personal expectations, social support, coping strategies, and access to information and treatment all influence the menopausal experience.

Many women find menopause liberating—freedom from menstruation, elimination of pregnancy concerns, relief from menstrual symptoms, and entry into a life phase focused on personal goals rather than child-rearing. Others struggle with symptoms, body changes, and what menopause represents about aging.

Maintaining perspective helps: menopause is a natural transition, not a disease (though it has medical implications requiring management). Symptoms are temporary for most women. Effective treatments exist. Women can thrive during and after menopause with appropriate support and management.

Connecting with other women navigating menopause provides validation and practical coping strategies. Many communities have menopause support groups, and online communities offer information and connection.

Self-advocacy is crucial. Many healthcare providers inadequately address menopause or dismiss women’s concerns. Women should feel empowered to seek providers knowledgeable about menopause, ask about treatment options, and insist on being taken seriously. Organizations like the North American Menopause Society (NAMS) provide directories of certified menopause practitioners.


Understanding menopause — its stages, symptoms, hormonal changes, treatment options, and long-term health implications — empowers women to make informed decisions, access appropriate care, and maintain health and quality of life during and after this significant transition.

Frequently Asked Questions
What’s the difference between cardiovascular disease and heart disease?

Cardiovascular disease is a broader term encompassing all diseases of the heart and blood vessels throughout the body, including coronary artery disease (affecting heart arteries), stroke (affecting brain arteries), peripheral artery disease (affecting leg arteries), and other vascular conditions. Heart disease specifically refers to conditions affecting the heart itself—primarily coronary artery disease, heart attack, heart failure, arrhythmias, and valve disease. While related and sharing common causes, cardiovascular disease is the umbrella term while heart disease is one category within it. For detailed information about heart-specific conditions, see our Heart Disease guide.

What causes most strokes?

Approximately 87% of strokes are ischemic strokes caused by blood clots blocking arteries supplying the brain. These clots either form in diseased brain arteries (thrombotic stroke) or travel from elsewhere, usually the heart in people with atrial fibrillation (embolic stroke). About 13% of strokes are hemorrhagic, caused by bleeding into or around the brain, usually from hypertension-damaged vessels or ruptured aneurysms. The underlying cause of most ischemic strokes is atherosclerosis—plaque buildup in arteries that narrows vessels and promotes clot formation. High blood pressure is the single most important modifiable stroke risk factor, increasing risk 3-4 fold. Other major contributors include diabetes, high cholesterol, smoking, atrial fibrillation, and obesity.

Can you prevent a stroke?

Yes—approximately 80% of strokes are preventable through risk factor management and lifestyle modifications. The most effective stroke prevention strategies are blood pressure control (reducing risk 30-40%), cholesterol management with statins (reducing risk 25%), smoking cessation (reducing risk 50%), diabetes management, maintaining healthy weight, regular physical activity, Mediterranean diet, and moderate alcohol consumption. For people with atrial fibrillation, anticoagulation prevents most strokes. After a TIA or previous stroke, aggressive secondary prevention including intensive blood pressure and cholesterol management, antiplatelet therapy, and addressing modifiable risk factors reduces recurrent stroke risk by 80%. The key is identifying and treating risk factors before stroke occurs, as prevention is far more effective than treatment after stroke.

What are the warning signs of a stroke?

Use the FAST acronym: Face drooping (ask person to smile, is smile uneven?), Arm weakness (ask person to raise both arms, does one drift down?), Speech difficulty (is speech slurred or incomprehensible?), Time to call 911 immediately if any signs present. Additional warning signs include sudden numbness or weakness (especially one-sided), sudden confusion, sudden vision problems in one or both eyes, sudden trouble walking or loss of balance, and sudden severe headache. Time is critical—stroke treatment is most effective within the first few hours. Even if symptoms resolve, call 911 immediately as this may be a TIA (warning stroke) indicating high risk of major stroke within days. Never wait to see if symptoms improve—immediate emergency response can mean the difference between minimal disability and devastating impairment or death.

What is peripheral artery disease and how do I know if I have it?

Peripheral artery disease (PAD) is narrowing of arteries carrying blood to the limbs, usually the legs, caused by atherosclerotic plaque buildup. PAD affects 8-12 million Americans but often goes undiagnosed. Classic symptom is claudication—cramping leg muscle pain triggered by walking and relieved by rest. The pain occurs at predictable walking distances, causes stopping, resolves within minutes, and recurs with renewed walking. PAD can also cause leg fatigue, coldness in lower leg or foot, weak pulses, or non-healing wounds. However, many people with PAD have no symptoms, particularly if sedentary. Risk factors include smoking (strongest association), diabetes, age over 65, high blood pressure, and high cholesterol. Screening involves ankle-brachial index (ABI)—comparing blood pressure in ankles to arms. Anyone with leg symptoms, significant cardiovascular risk factors, or history of heart disease or stroke should discuss PAD screening with their healthcare provider.

Is atherosclerosis reversible?

Early atherosclerosis is partially reversible with aggressive risk factor modification. Very intensive lipid lowering (achieving very low LDL cholesterol levels through high-dose statins plus additional agents), blood pressure control, diabetes management, smoking cessation, Mediterranean diet, regular exercise, and weight loss can halt atherosclerosis progression and cause modest regression of existing plaque. Imaging studies demonstrate that intensive statin therapy can reduce plaque volume by 5-10% over 1-2 years. However, advanced atherosclerosis with calcified plaque is less reversible. The more realistic goal is plaque stabilization—converting vulnerable plaque prone to rupture into stable plaque less likely to cause acute events. This occurs through reducing the lipid core, thickening the fibrous cap, and decreasing inflammation. Plaque stabilization dramatically reduces heart attack and stroke risk even without significant regression. This underscores why early intervention matters—starting prevention in young adulthood when atherosclerosis is minimal and reversible rather than waiting until advanced disease develops.

How often should I have my cardiovascular risk assessed?

Comprehensive cardiovascular risk assessment should include blood pressure measurement, lipid panel, fasting glucose, and calculation of 10-year cardiovascular risk score. For adults without known cardiovascular disease, assessment frequency depends on baseline risk: low-risk individuals (no risk factors, normal prior results) can be assessed every 4-5 years starting at age 40; moderate-risk individuals (1-2 risk factors) should be assessed every 2-3 years starting at age 35-40; high-risk individuals (multiple risk factors, strong family history, or abnormal prior results) should be assessed annually. Anyone with known cardiovascular disease, diabetes, or very high cardiovascular risk requires more frequent monitoring—typically every 3-6 months—to ensure risk factors remain optimally controlled. Blood pressure should be monitored more frequently, ideally with home monitoring. Risk assessment should begin earlier (age 20-30) in people with strong family history of premature cardiovascular disease or multiple risk factors.

Do I need medication if I have high cholesterol but no other risk factors?

Medication decisions depend on overall cardiovascular risk, not cholesterol alone. If your only risk factor is elevated LDL cholesterol with no other risk factors, you’re generally low risk and lifestyle interventions (diet, exercise, weight management) are tried first for 3-6 months. However, if LDL remains >190 mg/dL despite lifestyle changes, statin therapy is recommended regardless of other risk factors due to high LDL alone indicating substantial long-term risk. For more moderate cholesterol elevations, calculate your 10-year cardiovascular risk score incorporating age, blood pressure, cholesterol, diabetes status, and smoking. If 10-year risk exceeds 7.5-10%, statins are generally recommended. Additional factors influencing decisions include family history of premature cardiovascular disease, inflammatory markers like hsCRP, coronary calcium score, and patient preferences after informed discussion of benefits and risks. The key is assessing total cardiovascular risk, not treating cholesterol in isolation.

Can young people have cardiovascular disease?

Yes, though major cardiovascular events like heart attack and stroke are rare before age 45 in men and 55 in women. However, atherosclerosis begins in childhood or adolescence, with fatty streaks visible in arteries of teenagers. Young people with major risk factors—familial hypercholesterolemia (genetic very high cholesterol), diabetes, severe obesity, heavy smoking, or strong family history of premature cardiovascular disease—can develop significant atherosclerosis by their 20s or 30s. Additionally, certain conditions—severe hypertension, cocaine or methamphetamine use, autoimmune diseases like lupus, chronic kidney disease—dramatically accelerate atherosclerosis even in young people. Young adults with multiple risk factors should undergo cardiovascular risk assessment and intervention. The advantage of youth is that early intervention when atherosclerosis is minimal can prevent disease progression, making young adulthood the optimal time for establishing lifelong healthy habits and addressing modifiable risk factors.

What’s the connection between diabetes and cardiovascular disease?

Diabetes approximately doubles cardiovascular disease risk through multiple interconnected mechanisms. High blood sugar damages endothelium (arterial lining), accelerating atherosclerosis. Diabetes causes dyslipidemia (elevated triglycerides, low HDL, small dense LDL particles) promoting plaque formation. Diabetes increases inflammation and oxidative stress, both driving atherosclerosis. Diabetes impairs endothelial function and promotes blood clot formation. These mechanisms explain why cardiovascular disease is the leading cause of death in people with diabetes and why 2 in 3 people with diabetes die from cardiovascular causes. Importantly, intensive diabetes management—achieving HbA1c <7% through lifestyle and medications—reduces microvascular complications (retinopathy, nephropathy, neuropathy) but provides only modest cardiovascular benefit. More impactful for cardiovascular protection in diabetes are aggressive blood pressure control (target <130/80 mmHg), intensive lipid management with statins, antiplatelet therapy, smoking cessation, and weight management. Certain newer diabetes medications (GLP-1 agonists, SGLT2 inhibitors) also provide substantial cardiovascular benefits.

Should I take aspirin to prevent stroke?

Aspirin for primary prevention (preventing first stroke in people without known cardiovascular disease) has a less clear benefit-to-risk ratio than previously thought. Current guidelines recommend considering low-dose aspirin (81 mg daily) for primary prevention in people age 40-70 with elevated cardiovascular risk (10-year risk >10%) who are not at increased bleeding risk. The decision should be individualized, weighing modest cardiovascular benefit (10-20% relative risk reduction) against bleeding risk (particularly gastrointestinal bleeding and hemorrhagic stroke). Aspirin is not recommended for low-risk individuals or those over age 70 for primary prevention. However, for secondary prevention (after stroke, TIA, heart attack, or PAD diagnosis), aspirin or other antiplatelet agents are strongly recommended as they reduce recurrent cardiovascular events by 25%, substantially outweighing bleeding risks. For people with atrial fibrillation, anticoagulation (not aspirin) is needed for stroke prevention. Discuss aspirin with your healthcare provider considering your individual cardiovascular risk, bleeding risk, and preferences.

How much can lifestyle changes really reduce my cardiovascular risk?

Lifestyle interventions are remarkably effective for cardiovascular disease prevention, often approaching or exceeding medication benefits. Mediterranean diet reduces cardiovascular events by 30% in randomized trials—comparable to statin therapy. Regular physical activity (150 minutes moderate-intensity weekly) reduces cardiovascular events by 30-40%. Smoking cessation reduces cardiovascular risk by 50% within 1-2 years. Weight loss of 5-10% significantly improves blood pressure (1 mmHg per kg lost), cholesterol (triglycerides down 30-50%, HDL up 10-20%), and glucose metabolism. Combining interventions provides even greater benefit—one analysis found that adhering to five healthy lifestyle factors (not smoking, healthy weight, regular exercise, moderate alcohol, healthy diet) reduced cardiovascular disease risk by 80% compared to adhering to none. The challenge isn’t whether lifestyle changes work—abundant evidence confirms they do—but achieving sustainable behavior change. This is why comprehensive approaches addressing barriers to change, providing support, and celebrating progress work better than simply providing information.

References

This article provides comprehensive educational information about cardiovascular disease based on current clinical guidelines and peer-reviewed research. It does not replace personalized medical advice. Consult qualified healthcare professionals for diagnosis and treatment decisions specific to your situation.

Key Sources:

  1. Kleindorfer DO, Towfighi A, Chaturvedi S, et al. 2021 Guideline for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack. Stroke. 2021;52:e364-e467. https://www.ahajournals.org/doi/10.1161/STR.0000000000000375
  2. Gerhard-Herman MD, Gornik HL, Barrett C, et al. 2016 AHA/ACC Guideline on the Management of Patients With Lower Extremity Peripheral Artery Disease. Circulation. 2017;135:e726-e779. https://www.ahajournals.org/doi/10.1161/CIR.0000000000000471
  3. Visseren FLJ, Mach F, Smulders YM, et al. 2021 ESC Guidelines on cardiovascular disease prevention in clinical practice. European Heart Journal. 2021;42(34):3227-3337. https://academic.oup.com/eurheartj/article/42/34/3227/6358713
  4. Powers WJ, Rabinstein AA, Ackerson T, et al. Guidelines for the Early Management of Patients With Acute Ischemic Stroke. Stroke. 2019;50:e344-e418. https://www.ahajournals.org/doi/10.1161/STR.0000000000000211
  5. Berkhemer OA, Fransen PS, Beumer D, et al. A Randomized Trial of Intraarterial Treatment for Acute Ischemic Stroke. New England Journal of Medicine. 2015;372:11-20. https://www.nejm.org/doi/full/10.1056/NEJMoa1411587
  6. O’Donnell MJ, Chin SL, Rangarajan S, et al. Global and regional effects of potentially modifiable risk factors associated with acute stroke in 32 countries (INTERSTROKE). Lancet. 2016;388:761-775. https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(16)30506-2/fulltext
  7. Aboyans V, Ricco JB, Bartelink MEL, et al. 2017 ESC Guidelines on the Diagnosis and Treatment of Peripheral Arterial Diseases. European Heart Journal. 2018;39:763-816. https://academic.oup.com/eurheartj/article/39/9/763/4095038
  8. Criqui MH, Aboyans V. Epidemiology of Peripheral Artery Disease. Circulation Research. 2015;116:1509-1526. https://www.ahajournals.org/doi/10.1161/CIRCRESAHA.116.303849
  9. Murphy TP, Cutlip DE, Regensteiner JG, et al. Supervised Exercise, Stent Revascularization, or Medical Therapy for Claudication Due to Aortoiliac Peripheral Artery Disease. Journal of the American College of Cardiology. 2015;65:999-1009. https://www.jacc.org/doi/10.1016/j.jacc.2014.12.043
  10. Libby P, Buring JE, Badimon L, et al. Atherosclerosis. Nature Reviews Disease Primers. 2019;5:56. https://www.nature.com/articles/s41572-019-0106-z
  11. Ridker PM, Everett BM, Thuren T, et al. Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease. New England Journal of Medicine. 2017;377:1119-1131. https://www.nejm.org/doi/full/10.1056/NEJMoa1707914
  12. Estruch R, Ros E, Salas-Salvadó J, et al. Primary Prevention of Cardiovascular Disease with a Mediterranean Diet Supplemented with Extra-Virgin Olive Oil or Nuts. New England Journal of Medicine. 2018;378:e34. https://www.nejm.org/doi/full/10.1056/NEJMoa1800389
  13. Arnett DK, Blumenthal RS, Albert MA, et al. 2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease. Circulation. 2019;140:e596-e646. https://www.ahajournals.org/doi/10.1161/CIR.0000000000000678
  14. Goff DC Jr, Lloyd-Jones DM, Bennett G, et al. 2013 ACC/AHA Guideline on the Assessment of Cardiovascular Risk. Circulation. 2014;129:S49-S73. https://www.ahajournals.org/doi/10.1161/01.cir.0000437741.48606.98
  15. Tsao CW, Aday AW, Almarzooq ZI, et al. Heart Disease and Stroke Statistics—2022 Update. Circulation. 2022;145:e153-e639. https://www.ahajournals.org/doi/10.1161/CIR.0000000000001052
  16. Virani SS, Alonso A, Benjamin EJ, et al. Heart Disease and Stroke Statistics—2020 Update. Circulation. 2020;141:e139-e596. https://www.ahajournals.org/doi/10.1161/CIR.0000000000000757
  17. Centers for Disease Control and Prevention (CDC). Stroke Facts. https://www.cdc.gov/stroke/facts.htm
  18. American Heart Association. Peripheral Artery Disease. https://www.heart.org/en/health-topics/peripheral-artery-disease
  19. National Institute of Neurological Disorders and Stroke. Stroke Information Page. https://www.ninds.nih.gov/stroke
  20. World Health Organization. Cardiovascular diseases. https://www.who.int/health-topics/cardiovascular-diseases
Relevant Articles

Choose your region

We offer health testing services in select regions.