Women in the United States live an average of 5.1 years longer than men, with a female life expectancy of 79.3 years versus 74.2 years for males (CDC, 2022). This gap is driven by a combination of biological advantages, hormonal differences, immune system strength, and behavioral risk factors.
Key Takeaways
- Women outlive men by 5.1 years in the U.S. on average.
- Roughly 60% of the gap is biological; 40% is behavioral and modifiable.
- Estrogen delays cardiovascular disease by approximately 10 years in women.
- Men die from suicide at nearly 4x the rate of women.
- Black men have the lowest life expectancy of any U.S. demographic group at 70.8 years.
- Women live longer but spend more late-life years with chronic disability (the morbidity paradox).
The Life Expectancy Gap by the Numbers
The U.S. gender longevity gap is 5.1 years as of the most recent CDC data. This gap narrowed during the mid-20th century but has widened again since 2010, driven largely by rising male mortality from drug overdoses, suicide, and heart disease.
| Metric | Women | Men |
|---|---|---|
| U.S. Life Expectancy (2022) | 79.3 years | 74.2 years |
| Gap | 5.1 years | |
| Leading to cardiovascular death (avg age) | approx. 75 | approx. 65 |
| Cancer mortality rate (age-adjusted per 100,000) | approx. 133 | approx. 185 |
| Suicide rate (per 100,000) | approx. 6 | approx. 23 |
| Accidental death rate vs. women | 2x higher |
Biological Sex Differences Give Women a Built-In Advantage
Women’s chromosomal makeup directly protects them from certain genetic diseases. Females carry two X chromosomes (XX), while males carry one X and one Y (XY). Because many disease-linked genetic mutations are carried on the X chromosome, women have a backup copy, meaning a healthy second X can often compensate for a faulty one. Men, with only one X chromosome, have no such backup, making them more vulnerable to X-linked disorders (meaning conditions caused by mutations on the X chromosome, such as hemophilia).
This backup system is not trivial. Conditions including Duchenne muscular dystrophy, certain forms of color blindness, and X-linked immune deficiencies occur at dramatically higher rates in males precisely because they cannot compensate for a single defective X gene.
Estrogen Protects the Cardiovascular System
Estrogen (the primary female sex hormone) actively protects the heart and blood vessels throughout a woman’s reproductive years. It increases HDL cholesterol (the “good” cholesterol that removes plaque from arteries), decreases LDL cholesterol (the “bad” type that clogs vessels), and helps keep blood vessels flexible.
Men begin accumulating cardiovascular risk earlier because they lack this hormonal shielding. Heart disease is the number one killer of both sexes in the U.S., but men develop it on average 10 years earlier than women. After menopause (the permanent end of menstrual cycles, typically around age 51), women’s cardiovascular risk rises sharply as estrogen levels fall, but the decade-long head start women enjoy translates directly into longer lives.
| Cardiovascular Risk Factor | Women (Pre-Menopause) | Men (Same Age) |
|---|---|---|
| Average HDL cholesterol | Higher | Lower |
| Age of first heart attack (avg) | approx. 72 | approx. 65 |
| Hypertension onset | Later | Earlier |
| Arterial stiffness progression | Slower | Faster |
Women Have Stronger Immune Systems
The female immune system mounts faster, stronger responses to infections and vaccines. This is largely driven by genes on the X chromosome that regulate immune function (including the gene TLR7, a toll-like receptor that detects viral RNA). Because women have two copies of these genes, their immune response is more robust.
This immune advantage helps women fight off bacterial and viral infections more effectively, contributing to lower infectious disease mortality. The tradeoff is a higher rate of autoimmune diseases (conditions where the immune system attacks the body’s own tissues, such as lupus and rheumatoid arthritis) in women, but these conditions are rarely the direct cause of premature death at the same rate as heart disease or infection.
Testosterone Raises Male Risk in Several Ways
Testosterone (the primary male sex hormone) is associated with behaviors and physiological changes that increase mortality risk. High testosterone levels correlate with greater risk-taking behavior, aggression, reduced help-seeking behavior, and suppression of certain immune responses.
From a physiological standpoint, testosterone promotes red blood cell production and muscle mass but also increases levels of LDL cholesterol and promotes inflammatory pathways linked to heart disease. Men’s higher baseline levels of systemic inflammation (a chronic, low-grade immune activation that damages organs over time) are tied directly to testosterone’s effects on the body.
Behavioral and Social Factors Widen the Gap Substantially
Behavioral and social differences account for an estimated 40% of the U.S. gender longevity gap, making them the single largest modifiable driver of excess male mortality.
Risk-Taking and Accidental Death
Men account for approximately 73% of all accidental deaths in the U.S. Men are involved in more fatal car accidents, more occupational fatalities (men make up over 90% of workplace deaths), and higher rates of death from drowning, falls, and fires. Risk-tolerance, strongly influenced by testosterone and socialization, is a measurable mortality driver.
Suicide and Mental Health
Men die by suicide at nearly 4 times the rate of women in the U.S. Women attempt suicide more often, but men use more lethal methods and are less likely to seek mental health treatment. Cultural norms discouraging men from expressing emotional distress or seeking help are a recognized public health factor in premature male death.
Substance Use
Men consume alcohol at higher quantities and more frequently than women, and male alcohol-related death rates are 2 to 3 times higher. Men also have higher rates of smoking-related deaths and illicit drug overdose fatalities. The opioid crisis (a surge in deaths from opioid painkillers and heroin beginning around 2000) has disproportionately killed men.
| Behavioral Risk Factor | Male Rate vs. Female Rate |
|---|---|
| Suicide death rate | roughly 4x higher in men |
| Accidental death rate | roughly 2x higher in men |
| Alcohol-related death rate | 2 to 3x higher in men |
| Occupational fatality rate | roughly 9x higher in men |
| Drug overdose death rate | roughly 1.7x higher in men |
Men Use Healthcare Less, Later, and Less Effectively
Men in the U.S. are significantly less likely to have a primary care physician, less likely to schedule preventive screenings, and more likely to delay seeking care when symptoms appear. Studies show men are more likely to visit a doctor only after a condition has become serious, meaning diseases that are highly treatable when caught early, including certain cancers and hypertension (chronically elevated blood pressure), are more advanced at diagnosis in men.
Women are conditioned to engage with the healthcare system through reproductive health visits, prenatal care, and gynecological screenings beginning in their teens. This regular contact normalizes preventive medicine and leads to earlier detection of problems.
Cellular Aging Occurs Faster in Men
Men’s cells age faster than women’s at the chromosomal level, because men are born with shorter telomeres (the protective caps on the ends of chromosomes that function like biological aging clocks) and those telomeres shorten more rapidly throughout life. Shorter telomeres are associated with increased risk of age-related diseases including cancer, cardiovascular disease, and cognitive decline.
- Health age compares your life expectancy to the life expectancy of other Canadian 21 year old male. The difference is added or subtracted from your current age.
Research suggests estrogen may slow telomere shortening. Men’s faster cellular aging at the chromosomal level means their organs and tissues accumulate damage at a faster rate over a lifetime.
Men Carry More of the Dangerous Fat Type Even at the Same Body Weight
Even at identical body weight, men carry significantly more visceral fat (fat stored deep inside the abdominal cavity around organs) than women of the same age, while women store a greater share as subcutaneous fat (fat stored just beneath the skin, which is far less metabolically harmful). Visceral fat releases inflammatory compounds and drives insulin resistance (a condition where cells stop responding properly to insulin, raising blood sugar), type 2 diabetes, and cardiovascular disease.
This metabolic difference contributes meaningfully to men’s higher rates of metabolic syndrome (a cluster of conditions including high blood pressure, high blood sugar, and abnormal cholesterol that increase disease risk).
The Role of Mitochondria in Female Longevity
Women’s mitochondria (the energy-producing structures inside cells, often called the cell’s powerhouse) are better optimized for female biology because mitochondrial DNA is inherited exclusively through the maternal line. Evolutionary pressure has therefore optimized mitochondrial function around female physiology: mutations in mitochondrial DNA that are harmful to women get selected against, while mutations harmful only to males may be passed on undetected through generations.
This maternal inheritance bias means women may carry mitochondria that are more efficiently maintained and repaired over a lifetime, contributing to slower cellular aging and lower rates of mitochondrial dysfunction-linked diseases.
Historical Context: Has the Gap Always Existed?
The gender longevity gap has existed across recorded history but its size has varied considerably. In 1900, U.S. women outlived men by only about 2 years. The gap expanded to a peak of 7.8 years in 1975, driven largely by male deaths from smoking-related disease and cardiovascular disease before modern treatments existed.
Since the 1980s, the gap narrowed as smoking rates declined among men and cardiac care improved. Since 2010, the gap has widened again, largely because of the opioid epidemic and rising male suicide rates. The gap is not fixed; it reflects both fixed biology and changing social conditions simultaneously.
The Longevity Gap Exists in Every Country, But Varies Widely
The female longevity advantage exists in virtually every country worldwide, but the size of the gap varies significantly by national health systems, culture, and economic conditions.
| Country | Female Life Expectancy | Male Life Expectancy | Gap |
|---|---|---|---|
| Japan | 87.1 | 81.1 | 6.0 years |
| United States | 79.3 | 74.2 | 5.1 years |
| United Kingdom | 83.1 | 79.4 | 3.7 years |
| Russia | 77.2 | 66.5 | 10.7 years |
| India | 71.1 | 68.4 | 2.7 years |
Russia’s unusually large gap is attributed to extremely high male rates of alcohol consumption, smoking, and cardiovascular death. Countries with smaller gaps tend to have better male engagement with healthcare systems.
Race and Ethnicity Shape the Gap Within the United States
Race and ethnicity significantly shape both the size and the drivers of the gender longevity gap in the United States, with disparities ranging from 3.8 years for Asian Americans to 7.4 years for American Indian and Alaska Native populations. For Black men in particular, the gap is compounded by systemic healthcare disparities, higher rates of hypertension (chronically elevated blood pressure), and greater exposure to chronic stress from structural inequality.
| Group | Female Life Expectancy | Male Life Expectancy | Gap |
|---|---|---|---|
| Hispanic Americans | 84.0 years | 78.8 years | 5.2 years |
| White Americans | 80.5 years | 75.8 years | 4.7 years |
| Black Americans | 77.0 years | 70.8 years | 6.2 years |
| Asian Americans | 87.3 years | 83.5 years | 3.8 years |
| American Indian/Alaska Native | 75.1 years | 67.7 years | 7.4 years |
Black men face the most severe disadvantage, living an average of approximately 5 fewer years than white men and nearly 13 fewer years than Asian American women. Higher rates of uncontrolled hypertension, limited access to preventive care, higher incarceration rates (which independently shorten lifespan), and elevated chronic stress from systemic racism all contribute to this disparity.
The Hispanic paradox (formally called the epidemiological paradox) refers to the well-documented finding that Hispanic Americans live longer than white Americans despite having lower average incomes and less health insurance coverage. Proposed explanations include stronger family social support networks, lower rates of smoking, and the “healthy immigrant effect” (meaning recent immigrants tend to be healthier than the average population in their origin country and arrive in better health than native-born Americans).
Men Are Disproportionately Killed by COVID-19
Men accounted for approximately 54 to 57% of U.S. COVID-19 deaths despite making up roughly half the population (CDC COVID tracking data). COVID-19 revealed and amplified existing biological sex differences in immune response across every country where sex-disaggregated data was collected.
The male disadvantage was driven by several converging factors: men’s weaker innate immune response to viral infection, higher baseline rates of cardiovascular disease and type 2 diabetes (both severe COVID risk factors), higher rates of smoking-related lung damage, and lower rates of mask use and vaccination uptake.
The pandemic measurably widened the U.S. longevity gap, which jumped from 5.0 years in 2019 to 5.7 years in 2021 before beginning to narrow again as excess COVID deaths declined.
Sleep Apnea Strikes Men Far More Often
Men are 2 to 3 times more likely than women to develop obstructive sleep apnea (a condition where the airway repeatedly collapses during sleep, causing the body to repeatedly wake to resume breathing). Sleep apnea is severely underdiagnosed in men because many never report symptoms to a physician.
Untreated sleep apnea raises the risk of hypertension, heart disease, stroke, and type 2 diabetes. Men with severe untreated sleep apnea have cardiovascular death rates that are measurably higher than men without the condition. Anatomical factors including greater neck circumference and different patterns of fat distribution around the airway make men structurally more susceptible. Testosterone also promotes upper airway instability during sleep. Because many men avoid doctors and never receive a formal diagnosis, this condition operates as a silent mortality driver at population scale.
Diet Differences Add Up Over Decades
Men in the United States consume significantly less healthy diets than women on average, and this behavioral gap compounds biological disadvantage over decades. Men eat more red and processed meat, more sodium, more saturated fat, and fewer fruits and vegetables than women. Men are also less likely to follow dietary guidelines or actively track nutritional intake.
| Dietary Factor | Men (U.S. Average) | Women (U.S. Average) |
|---|---|---|
| Daily sodium intake | 3,800 mg | 2,800 mg |
| Daily fruit and vegetable servings | Fewer | More |
| Red meat consumption | Higher | Lower |
| Adherence to dietary guidelines | Lower | Higher |
| Daily added sugar intake | Higher | Lower |
The U.S. Dietary Guidelines recommend no more than 2,300 mg of sodium per day. Men exceed this limit by an average of 65%, directly contributing to higher blood pressure and cardiovascular risk. The cumulative effect of consistently poorer diet choices over 30 to 40 years translates into measurably worse metabolic health outcomes at older ages.
Brain Disease Falls Differently by Sex
Men are approximately 1.5 times more likely to develop Parkinson’s disease (a progressive neurological disorder causing tremors, stiffness, and movement impairment) than women. Testosterone may promote the dopamine neuron loss that drives Parkinson’s, while estrogen has shown neuroprotective effects in laboratory studies.
Women represent approximately two-thirds of all Americans living with Alzheimer’s disease (the most common form of dementia, involving progressive memory loss and cognitive decline). This is partly explained by women living longer, since age is the strongest Alzheimer’s risk factor. Women who carry the APOE4 gene (the strongest known genetic risk factor for Alzheimer’s) also develop the disease more aggressively than men carrying the same gene, suggesting genuine biological susceptibility beyond age alone.
The result is a divergence: men die earlier from cardiovascular and neuromotor diseases, while women live longer but are more likely to spend later years managing cognitive decline.
The Morbidity Paradox: Living Longer Does Not Always Mean Living Better
Women live longer than men but spend more years of late life in poor health, a tradeoff researchers call the morbidity paradox (morbidity meaning the presence of illness or disability, as opposed to mortality meaning death). Men are more likely to die quickly from acute events like heart attacks; women are more likely to survive those events but accumulate chronic conditions over a longer life.
Women have higher lifetime rates of arthritis, osteoporosis (reduced bone density that increases fracture risk), depression, anxiety, chronic pain conditions, and autoimmune diseases.
| Condition More Common in Women | Approximate Female-to-Male Ratio |
|---|---|
| Osteoporosis | 4x more common in women |
| Rheumatoid arthritis | 2 to 3x more common in women |
| Lupus (autoimmune disease) | 9x more common in women |
| Depression (diagnosed) | 2x more common in women |
| Alzheimer’s (total patients) | roughly 2x more women than men |
Researchers measure this tradeoff using disability-adjusted life years (DALYs), a metric combining years of life lost to premature death with years lived with disability. When DALYs are calculated, men’s shorter lives and women’s more disability-burdened later years bring the two sexes closer together in total healthy lifespan than raw life expectancy numbers suggest.
Can Men Close the Gap?
Men can meaningfully extend their lives by adopting behaviors that address the modifiable risk factors. The biological disadvantage is real but not decisive: roughly 40% of the life expectancy gap is estimated to be behavioral and social in origin, meaning it is potentially changeable.
- Engage in preventive healthcare by establishing a primary care provider and completing recommended screenings (colonoscopy starting at 45, blood pressure checks, cholesterol panels).
- Reduce cardiovascular risk through regular aerobic exercise (at least 150 minutes per week), a diet low in saturated fat, and maintaining healthy weight.
- Limit alcohol to no more than 2 standard drinks per day per U.S. dietary guidelines.
- Seek mental health support proactively rather than only in crisis. Men who access therapy show reduced all-cause mortality in long-term studies.
- Wear seatbelts, use safety equipment at work, and reduce unnecessary physical risk. Preventable accidents are a disproportionate male mortality driver.
- Quit smoking or never start. Smoking remains one of the most powerful reducers of life expectancy for both sexes.
- Manage stress through sleep (7 to 9 hours nightly), exercise, and social connection. Men with strong social networks live measurably longer.
FAQs
Why do women live longer than men scientifically?
Women benefit from estrogen’s cardiovascular protection, a stronger immune system backed by two X chromosomes, slower cellular aging due to longer telomeres, and less visceral fat accumulation. Combined with behavioral factors like lower rates of smoking, alcohol abuse, and risk-taking, these advantages compound over a lifetime.
How many more years do women live than men in the U.S.?
In the United States, women live an average of 5.1 years longer than men, with a female life expectancy of 79.3 years versus 74.2 years for males as of 2022 CDC data.
Does estrogen actually protect the heart?
Yes. Estrogen raises HDL cholesterol (the protective type), lowers LDL cholesterol, and keeps blood vessel walls flexible. These effects delay the onset of cardiovascular disease by approximately 10 years in women compared to men.
Why do men have more heart attacks than women?
Men lack estrogen’s cardiovascular shielding, carry more visceral fat (which releases inflammatory compounds), and develop arterial plaque earlier in life. The average age of a first heart attack is 65 for men versus 72 for women.
Is the gender longevity gap biological or behavioral?
Both. Roughly 60% of the gap is estimated to be biological in origin (chromosomes, hormones, immune function, cellular aging). The remaining 40% is tied to behavioral differences including substance use, risk-taking, and healthcare avoidance.
Do men visit the doctor less than women?
Yes. Studies consistently show men are less likely to have a primary care provider, less likely to attend preventive screenings, and more likely to delay care until a condition is serious. This healthcare avoidance contributes meaningfully to premature male mortality.
Why do men die from suicide more than women?
Men die by suicide at nearly 4 times the rate of women in the U.S. Men tend to use more lethal methods, are less likely to disclose suicidal thoughts, and are significantly less likely to seek mental health treatment due to cultural stigma around male emotional vulnerability.
Does testosterone shorten lifespan?
Testosterone is associated with higher cardiovascular risk, greater risk-taking behavior, and some suppression of immune function. Studies of castrated males historically showed longer lifespans, suggesting testosterone does impose some longevity cost, though the effect is complex and not a reason for men to pursue hormonal alteration.
Are women’s immune systems actually stronger than men’s?
Women mount stronger, faster immune responses to infections and vaccines. Genes on the X chromosome (including TLR7) regulate immune function, and women’s two copies amplify this response. The tradeoff is higher rates of autoimmune diseases in women, but these do not reduce longevity to the same degree as infectious or cardiovascular diseases.
What is the role of telomeres in the longevity gap?
Telomeres are protective chromosome caps that shorten as cells divide. Women are born with longer telomeres and they shorten more slowly, meaning women’s cells age at a slower biological rate. Estrogen is believed to slow telomere shortening, contributing to this advantage.
Why does Russia have such a large gender longevity gap?
Russia’s gap exceeds 10 years, driven primarily by extremely high rates of male alcohol consumption, heavy smoking, cardiovascular disease, and a weak preventive healthcare culture among men. It represents an extreme version of behavioral and systemic factors that widen the gap globally.
Does the longevity gap exist in every country?
Yes. The female longevity advantage exists in virtually every country ever studied. The size of the gap varies from under 2 years in some developing nations to over 10 years in Russia, shaped by culture, healthcare access, male behavior, and economic conditions.
Did women always outlive men throughout history?
The gap has existed throughout recorded history but was smaller in the past. In 1900, U.S. women outlived men by only about 2 years, largely because childbirth complications killed many women. As maternal mortality fell, the biological and behavioral advantages of female biology became fully expressed.
What kills men most often before age 65?
Heart disease is the leading cause of premature male death in the U.S. Drug overdoses, suicide, accidental injury, and liver disease (often alcohol-related) are the next most significant contributors to excess male mortality before age 65.
Is the longevity gap closing or widening?
The gap narrowed from its peak of 7.8 years in 1975 to about 4.8 years by 2010, but has been widening again since then. The opioid epidemic and rising male suicide rates are the primary drivers of the recent widening trend.
Can lifestyle changes help men live as long as women?
Men who avoid smoking, drink in moderation, exercise regularly, maintain healthy weight, engage with healthcare preventively, and manage mental health can substantially reduce their mortality risk. Behavioral factors account for an estimated 40% of the gap, meaning they are meaningful but cannot fully eliminate the biological component.
Why do women have less visceral fat than men?
Estrogen directs fat storage toward subcutaneous deposits (under the skin) rather than visceral deposits (around internal organs). Visceral fat is far more metabolically harmful, releasing inflammatory proteins and contributing to insulin resistance, diabetes, and cardiovascular disease.
What happens to the longevity gap after menopause?
Women’s cardiovascular risk rises significantly after menopause as estrogen levels fall. However, because women spend decades with hormonal protection during their reproductive years, the damage accumulated in their cardiovascular system is far less than in men of comparable age. The head start cannot be erased by post-menopausal hormonal changes alone.
Does social support affect longevity differently for men and women?
Yes. Men with strong social networks live meaningfully longer than socially isolated men. Women tend to maintain broader, more emotionally supportive social connections throughout life, while men’s social networks often shrink significantly after retirement or the death of a spouse. Social isolation is a recognized mortality risk factor that disproportionately affects older men.
Are there genetic diseases that affect men more than women?
Yes. X-linked disorders including hemophilia, Duchenne muscular dystrophy, and certain forms of immune deficiency affect males almost exclusively because men have only one X chromosome and cannot compensate for a defective gene with a healthy backup copy as women can.
Why do men have higher cancer death rates than women?
Men’s cancer mortality rate is approximately 185 per 100,000 versus 133 per 100,000 for women. Men are more likely to smoke (historically), engage in occupations with carcinogen exposure, delay cancer screenings, and present with later-stage disease. Biological factors including immune differences also contribute to men’s higher cancer fatality rates.
Does marriage affect the longevity gap?
Married men live significantly longer than unmarried men, with a more pronounced effect than marriage has on women’s longevity. Married men are more likely to have a regular healthcare connection (often managed by a spouse), healthier diets, lower alcohol consumption, and stronger social support. The “marriage benefit” for longevity is stronger for men than for women.
Why do Black men have a shorter life expectancy than other groups?
Black men in the U.S. have a life expectancy of approximately 70.8 years, the lowest of any major demographic group. Higher rates of uncontrolled hypertension, limited access to preventive healthcare, higher incarceration rates (which shorten lifespan independently), and the physiological effects of chronic stress from systemic racism all contribute to this disparity.
What is the Hispanic paradox in life expectancy?
The Hispanic paradox refers to the fact that Hispanic Americans live longer than white Americans despite lower average incomes and lower rates of health insurance coverage. Hispanic men live to approximately 78.8 years on average, 3 years longer than white men. Strong family social support networks, lower smoking rates, and the healthy immigrant effect (immigrants arriving in better-than-average health) are the leading explanations.
Did COVID-19 change the gender longevity gap?
Yes. Men died from COVID-19 at significantly higher rates than women, accounting for approximately 54 to 57% of U.S. COVID deaths despite being roughly half the population. The U.S. longevity gap widened from 5.0 years in 2019 to 5.7 years in 2021 before beginning to narrow again, with COVID-19 mortality being a primary driver of that widening.
Does sleep apnea affect life expectancy in men?
Yes. Men are 2 to 3 times more likely than women to develop sleep apnea, and untreated sleep apnea significantly raises the risk of hypertension, heart disease, and stroke. Because many men avoid doctors and go undiagnosed, sleep apnea operates as a largely silent cardiovascular mortality driver at population scale, contributing to the longevity gap.
Do women live longer but in worse health than men?
This is known as the morbidity paradox. Women live longer but experience higher lifetime rates of disability, chronic pain, arthritis, osteoporosis, autoimmune diseases, and depression. Men are more likely to die quickly from acute events; women are more likely to survive but accumulate chronic conditions. When total healthy lifespan is measured rather than raw life expectancy, the gap between men and women narrows considerably.
Why do women get Alzheimer’s more than men?
Women represent approximately two-thirds of Americans living with Alzheimer’s disease. This is partly because age is the strongest Alzheimer’s risk factor and women live longer. However, women who carry the APOE4 gene (the strongest genetic risk factor for Alzheimer’s) develop the disease more aggressively than men with the same gene, suggesting genuine biological susceptibility differences beyond age alone.
Does diet explain part of the longevity gap between men and women?
Yes. Men in the U.S. consume significantly more sodium (averaging 3,800 mg per day versus the 2,300 mg recommended limit), more red and processed meat, and fewer fruits and vegetables than women. These dietary differences compound biological cardiovascular disadvantages over decades and contribute measurably to men’s higher rates of hypertension, heart disease, and metabolic syndrome.
Do men get Parkinson’s disease more than women?
Yes. Men are approximately 1.5 times more likely than women to develop Parkinson’s disease. Testosterone may accelerate the loss of dopamine-producing neurons that drives Parkinson’s, while estrogen appears to offer some neuroprotective effect. This neurological disadvantage is one more biological factor reducing male lifespan relative to female lifespan.