
Why do women live longer than men?
This holds regardless of where women live, how much money they make, and many other factors. It's even true for most other mammals.
'It's a very robust phenomenon all over the world, totally conserved in sickness, during famines, during epidemics, even during times of starvation,' said Dr. Dena Dubal, a professor of neurology at the University of California, San Francisco.
But the reasons women live longer are complicated and less established — and the fact that they are outliving men doesn't necessarily mean they are living better. Women tend to have shorter health spans (the number of healthy years a person lives) than men, said Bérénice Benayoun, an associate professor at the USC Leonard Davis School of Gerontology. Women are generally more physically frail than men in old age; they're also more vulnerable, particularly after menopause, to developing cardiovascular issues and Alzheimer's disease, in part because age itself is a risk factor for those conditions, Benayoun said.
Scientists are trying to uncover the reasons men and women age differently in the hopes of extending the life span and health span for both.
'If we can understand what makes one sex more resilient or vulnerable, then we have new pathways, new molecular understanding, for new therapeutics that could help one or both sexes also be resilient,' Dubal said.
Here's what they know so far about what causes the longevity gap.
Genetics
A growing body of research suggests that the XX set of female sex chromosomes (which, along with other chromosomes, carry our DNA) may impact longevity, though it's not clear exactly how. For example, a 2018 study conducted by Dubal's lab looked at genetically manipulated mice with different combinations of sex chromosomes and reproductive organs. Those with two X chromosomes and ovaries lived longest, followed by mice with two X chromosomes and testes. Mice with XY chromosomes had shorter life spans.
'There was something about the second X chromosome that was protecting the mice from dying earlier in life, even if they had testes,' Dubal said. 'What if there was something on that second X chromosome that was in some ways a sprinkle of the fountain of youth?'
Scientists haven't yet examined this in humans, but Dubal said the fact that we have the same hormones and sex chromosomes and similar reproductive systems suggests that the findings could be similar in people.
Epigenetic factors — environmental or lifestyle elements like climate or chronic stress that impact which genes are expressed, and how — may also play a role in life span, widening or shrinking the disparities between men and women, said Montserrat Anguera, an associate professor of biomedical sciences at the University of Pennsylvania School of Veterinary Medicine, who studies this topic.
Hormones
Researchers are also investigating the role of sex hormones like estrogen in longevity and are especially interested in the effect they have on the immune system. 'Decent data is showing that, at least before menopause, the female immune system tends to be better, more on it and better able to mount responses,' Benayoun said. In general, males 'tend to do much worse in response to infection,' which in turn could shorten their life spans; they're also more likely than women to die of sepsis, she said.
One 2017 analysis found that women who experienced menopause later in life — older than 50 — lived longer than those who experienced it earlier. When estrogen levels drop, such as during menopause, women's immune systems seem to weaken. Women tend to catch up to (or surpass) men in terms of developing diseases that were less common before menopause, Benayoun said.
Lifestyle and Behavior
Behavioral patterns play a key role in the disparity. Women are generally less likely than men to smoke or drink heavily — behaviors that contribute significantly to mortality, said Kyle Bourassa, a psychologist and a senior fellow at the Center for the Study of Aging and Human Development at Duke University.
Women also tend to practice more 'health-promoting behavior,' like wearing a seat belt or going to the doctor for annual checkups, Bourassa said. In addition, he said that women are more likely than men to socialize, protecting them from the detrimental effects of social isolation and loneliness. A 2023 analysis found they're also less likely to die by drug overdose or suicide.
External Factors
On a broader societal level, issues like war or gun violence disproportionately impact men, said Naoko Muramatsu, a professor of community health sciences at the University of Illinois Chicago.
During the COVID pandemic, men died at higher rates than women. Research showed that they were more likely to hold jobs that exposed them to the virus, like food preparation or construction, or to be homeless or incarcerated, all of which affected mortality rates.
Ultimately, it's a combination of all these factors that determines the life span gap, said Alan Cohen, an associate professor of environmental health sciences at Columbia University Mailman School of Public Health. 'There's probably a thousand ways that that's happening.'
And even though we do have control over some factors, like drinking, smoking and diet, it's not yet clear how significantly longevity would be impacted by changing those behaviors, Bourassa said.
'We need randomized control trials to tease these things apart,' he said.
This article originally appeared in
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Observer
2 days ago
- Observer
Once a death sentence, this heart condition is finally treatable
When James Hicks, 75, was diagnosed with heart failure, it felt like the beginning of the end. Hicks, a former railroad worker from Rogers, Arkansas, had quietly dealt with various health problems, from carpal tunnel syndrome in both arms to dual knee replacements. But now his heart was giving out, and the doctors chalked it up to the wear and tear of old age. 'There's just not exactly a surgery to fix this,' he said. Soon enough, Hicks couldn't walk from his grandson's high school basketball game to the car, without stopping several times to catch his breath. His feet and ankles would swell if he didn't elevate them. He could feel his heart racing uncontrollably, unable to find a steady rhythm. Hicks' doctors tried a half-dozen different medications, but nothing really helped. It wasn't until 2023, some 10 years after the original diagnosis, that a local cardiologist raised the possibility of cardiac amyloidosis, a little-known form of heart failure. Over the past 50 years, heart failure has become one of the fastest-growing cardiac killers. It was long considered a disease of aging, caused by gradual yet unavoidable changes to the heart. But doctors are now discovering that about 15% of cases are caused by a rogue protein called amyloid, perhaps best known for its role in Alzheimer's. While one type tangles neurons in the brain, others infiltrate the heart, making the muscle stiff and less able to pump blood. Until recently, cardiac amyloidosis was a death sentence, but the advent of new medications, including two approved by the Food and Drug Administration in the past year, have made this disease increasingly manageable. 'We shouldn't just be fatalistic — 'you're tired, you're short of breath, you're just old,' ' said Dr. Michelle Kittleson, a cardiologist at Cedars-Sinai Medical Center. 'There is a lot of hope for people with heart failure.' Diagnoses on the Rise For decades, cardiac amyloidosis was cast aside as a rare disease. Early signs include carpal tunnel syndrome, a narrowing of the spine and a rupture of the biceps tendon, as amyloid plaques accumulate across the body. But with little awareness of the condition, it was difficult for doctors to connect the dots. And there was little incentive to do so, Kittleson said, because without any treatments for cardiac amyloidosis, they could only stand by and watch patients succumb to the disease. To get diagnosed, then, was like stepping into the darkness, said Ozzie Giglio, 64, who learned he had cardiac amyloidosis in 2016. He recalled his doctor saying, 'I want to get you on the heart transplant list right away. That's the only way to save your life.' But as researchers developed easier ways to spot cardiac amyloidosis, more patients were diagnosed, said Mathew Maurer, a cardiologist at Columbia University Irving Medical Center. Instead of needing to biopsy the heart, doctors can now use a scan that lights up amyloid plaques, and test patients' blood and urine for the abnormal protein, he added. However, the turning point for cardiac amyloidosis was the development of effective treatments. With doctors now able to help patients, there was an 'explosion in recognition,' Kittleson said. Experts believe cardiac amyloidosis is most common among men, adults 75 or older, and Black people. But nobody knows for sure, since many patients aren't tested. 'I can't give you a prevalence estimate, but clearly, we're at the tip of the iceberg in older populations,' Kittleson said. The New Drugs Are Lifesaving What makes cardiac amyloidosis so deadly is that the abnormal protein gets between the fibers of the heart, stiffening the muscle and impairing the heart's rhythm, said Dr. Pablo Quintero Pinzon, a cardiologist at Beth Israel Deaconess Medical Center. Some forms are hereditary; others occur spontaneously for reasons experts don't yet understand. Two types of misfolded proteins usually cause cardiac amyloidosis, but the new drugs target only one of them, transthyretin, either silencing its production or stabilizing the molecule so that it doesn't infiltrate the heart, Quintero said. Trials published in the New England Journal of Medicine — and funded by pharmaceutical companies — showed that these new drugs (tafamidis, acoramidis, and vutrisiran) preserved quality of life and reduced deaths by 25 to 35% compared to a placebo. In the most recent trial, patients on vutrisiran lived nearly as long as the general population. 'We might be living in an era where you will die with cardiac amyloidosis as opposed to from it,' Kittleson said. The Journal of the American College of Cardiology dedicated its latest issue to cardiac amyloidosis. New research shows how vutrisiran improves some measures of heart relaxation and muscle damage, while staving off further declines in heart contraction and wall stress. With the current diagnostic tools, there aren't good ways to know if patients with cardiac amyloidosis are responding to treatment. But these new findings suggest that doctors can use echocardiogram scans and blood-based biomarkers to monitor patients' progress and potentially predict survival, said Quintero, who was not involved in this research. When Marc Israel was diagnosed with the disease in 2020, doctors told him he could expect to live 12 to 18 months without treatment. But Israel, 77, was quickly able to get on tafamidis. 'And here I am, five years later,' he said. Several Questions Remain For all their benefits, these drugs don't cure the disease; they just 'freeze' patients at whatever stage of heart failure they're in, Kittleson said. The ability of the medications to reduce the risk of death also drops precipitously as time goes on. That's why early diagnosis is so important, and why researchers are eagerly awaiting results for a new drug designed to remove amyloid from the heart even after it's built up. There's also still a question of how many patients will be able to afford the drugs. They are incredibly expensive, costing $250,000 to $500,000 per year. Medicare covers all three medications, so most patients won't pay more than $2,000 out of pocket each year. But that's still a heavy burden on the broader health care system, Maurer said. For patients, the treatment can be life-changing. With his cardiac amyloidosis and irregular heartbeats under control, Hicks has gone back to riding his e-bike 100 miles every week and lifting dumbbells in his home gym. 'I don't feel 75 years old anymore; I feel much younger,' he said. 'It's hard to think that I've got some disease in my body.' This article originally appeared in


Observer
04-08-2025
- Observer
‘Japanese Walking' is a fitness trend worth trying
Going for a walk is one of the simplest workouts, but it can have powerful health impacts. Walking has been linked to improved mental and cardiovascular health, and it can be effective for managing back pain. But not all walking is equally effective. A method nicknamed 'Japanese walking' on social media — also known as interval walking training, or IWT — seems to offer greater advantages than a simple stroll, or even than walking at a moderate pace for 8,000 or more steps a day. The strategy was first introduced two decades ago in a study led by Hiroshi Nose, an exercise physiologist at Shinshu University Graduate School of Medicine in Japan. The country has one of the world's oldest populations, and Nose hoped that, by applying interval-training techniques used by elite athletes to its senior community, he could improve older people's health and reduce the country's medical costs, he told The New York Times in an email. After seeing promising early results, he and his collaborator, Shizue Masuki, continued to study the method in depth. While this type of exercise isn't new, it has been a trend on TikTok this summer. Here's what the science says about the benefits of interval walking and how to get started. What is 'Japanese walking'? As the name suggests, interval walking is a form of interval training, which involves alternating between bursts of intense activity and more gentle movement or rest. In this case, it's basically just alternating between fast and slow walking. But compared with more classic forms of high-intensity interval training, interval walking is more approachable for many people, especially those who haven't exercised in a while or who are recovering from injuries that make high-impact activities like running difficult, said Dr. Carlin Senter, the chief of primary-care sports medicine at the University of California, San Francisco. How do you do it? All you need are comfortable shoes, a safe place to walk, and a timer. In the studies by Nose and Masuki, subjects typically walked quickly for three minutes and then slowly for three minutes. During fast periods, the idea is to feel as if you're working somewhat hard, to the point that you would have a hard time carrying on a conversation. The movement during the slow periods should be a gentle stroll. (The researchers capped the fast intervals at three minutes, they said, because that was the point at which many older volunteers started to feel tired.) They recommend taking longer strides during the fast intervals than during the slow ones, to make the activity more challenging. They also suggest engaging your arms, bending them at the elbows, and swinging them vigorously with each step, which will help you maintain proper form during longer strides. In their studies, volunteers completed at least 30 minutes of interval walking four times a week. If you try it, those 30 minutes don't have to be continuous. The research suggests that breaking the sessions into roughly 10-minute segments three times a day can be just as effective. While conducting their research, they found that, by taking regular recovery breaks, many interval walkers spent more time exercising at a high intensity than they would have if they had walked continuously at that intensity, since they tired out sooner when they didn't have breaks. What are the health benefits? In their original study of older adults, which was small, Nose and Masuki found that interval walkers saw significantly greater improvements in blood pressure, cardiovascular health, and leg strength compared with volunteers who walked at a continuous, moderate pace. In the decade since, a growing body of evidence from Nose and Masuki and other researchers has reinforced these findings and has suggested the method may have even more benefits. A 2018 study found that, over 10 years, interval walking was linked to fewer age-related declines in aerobic capacity and muscle power. What's the best way to add interval walking to your exercise routine? If you haven't been active in a while, 'start low, go slow,' Senter said. If three minutes feels too long for the faster intervals, start with a minute and work your way up. Over time, as your fitness improves, you will probably be able to push yourself harder during the fast bouts. Finally, if interval walking is your main form of exercise, aim to complement it with at least two days a week of strength training, along with balance and mobility training, Senter said. This article originally appeared in


Observer
24-03-2025
- Observer
Extreme Heat Linked to Accelerated Aging in Older Adults, Study Finds
Extreme heat poses significant hazards for older individuals, increasing their vulnerability to heatstroke and mortality. Recent research suggests that elevated temperatures may also influence DNA functioning, potentially accelerating the aging process itself. A groundbreaking study published in Science Advances explored this concept by analyzing data from over 3,600 older adults across the United States. The researchers discovered that individuals residing in neighborhoods frequently experiencing extreme heat—defined as temperatures of 90 degrees Fahrenheit or above—exhibited more rapid biological aging at a molecular level compared to those living in areas with fewer instances of extreme heat. The implications are profound, linking heat waves exacerbated by climate change to chemical modifications in DNA that could hasten biological aging. The researchers estimate that individuals in regions where temperatures soar to 90 degrees or higher for 140 days or more annually may age approximately 14 months quicker than peers in locales with fewer than 10 days of extreme heat each year. The study utilized three aging biomarkers known as epigenetic clocks, derived from blood samples of individuals aged 56 and older involved in a national population study. Researchers correlated these biomarker age estimates with six years of daily climate data across different geographical locations. These epigenetic clocks serve as measures of biological changes that can predict future risks of disease or mortality linked to advanced age. According to Eun Young Choi, a postdoctoral associate at USC Leonard Davis School of Gerontology and co-author of the study, while DNA remains constant since birth, external influences like stress and pollution can instigate molecular changes, activating or deactivating genes and modifying their functionality. Choi likened DNA to a blueprint and epigenetic modifications to a switchboard controlling which aspects of that blueprint become active. This research represents the first population-scale analysis linking heat exposure to epigenetic aging in humans, building upon earlier studies that indicated similar changes in species such as fish, mice, and guinea pigs. Health expert Nancy Krieger from Harvard T.H. Chan School of Public Health noted that this research provides valuable insights into geographical health discrepancies. However, the study does not establish causation; it indicates a correlation between heat exposure and accelerated aging. The researchers highlighted that additional factors may contribute, as the analysis lacked lifestyle variables like air conditioning access or time spent indoors. Some scientists remain skeptical about the efficacy of epigenetic clocks as definitive aging measures, as noted by Rachel Morello-Frosch from UC Berkeley. The ongoing research in this area raises questions about biomarkers and their predictive capabilities regarding future health outcomes. Furthermore, not all epigenetic changes are negative. The study does not clarify if these changes might reflect adaptive responses to heat, such as increased indoor activity. Environmental epidemiologist Greg Wellenius emphasized that demonstrating cellular-level changes is an essential step toward understanding heat's impact on health. Significant questions remain: What roles do air conditioning and other interventions play in epigenetic aging? Can short-term exposure to extreme heat have lasting effects? Can relocating from hot areas reverse aging? Jennifer Ailshire from USC Leonard Davis highlighted the necessity for longitudinal data to comprehensively understand these dynamics. This study lays the groundwork for future investigations into interventions, such as increased access to air conditioning and shady environments, potentially mitigating heat-related aging effects. Mariana Arcaya from MIT pointed out the prevailing focus on emergency medical interventions for heat survival, underlining that this research highlights potential long-term health effects from heat, even in those who do not face immediate medical crises. —NYT