Every year I ask the college students in the course I teach about the 14th-century Black Death to imagine they are farmers or nuns or nobles in the Middle Ages. What would their lives have been like in the face of this terrifying disease that killed millions of people in just a few years?
Setting aside how they envision what it would be like to confront the plague, these undergrads often figure that during the medieval period they would already be considered middle-aged or elderly at the age of 20. Rather than being in the prime of life, they think they’d soon be decrepit and dead.
They’re reflecting a common misperception that long life spans in humans are very recent, and that no one in the past lived much beyond their 30s.
One of the first steps in research about demography in the past is to estimate how old people were when they died. Bioarchaeologists do this using information about how your bones and teeth change as you get older.
For example, I look for changes to joints in the pelvis that are common at older ages. Observations of these joints in people today whose ages we know allow us to estimate ages for people from archaeological sites with joints that look similar.
Another way to estimate age is to use a microscope to count the yearly additions of a mineralized tissue called cementum on teeth. It’s similar to counting a tree’s rings to see how many years it lived. Using approaches like these, manystudies have documented the existence of people who lived long lives in the past.
Given physical and historical evidence that many people did live long lives in the past, why does the misperception that everyone was dead by the age of 30 or 40 persist? It stems from confusion about the difference between individual life spans and life expectancy.
Life expectancy is the average number of years of life remaining for people of a particular age. For example, life expectancy at birth (age 0) is the average length of life for newborns. Life expectancy at age 25 is how much longer people live on average given they’ve survived to age 25.
In medieval England, life expectancy at birth for boys born to families that owned land was a mere 31.3 years. However, life expectancy at age 25 for landowners in medieval England was 25.7. This means that people in that era who celebrated their 25th birthday could expect to live until they were 50.7, on average – 25.7 more years. While 50 might not seem old by today’s standards, remember that this is an average, so many people would have lived much longer, into their 70s, 80s and even older.
Life expectancy is a population-level statistic that reflects the conditions and experiences of a huge variety of people with very different health conditions and behaviors, some who die at very young ages, some who live to be over 100 years old, and lots whose life spans fall somewhere in between. Life expectancy is not a promise (or a threat!) about the life span of any single person.
What some people don’t realize is that low life expectancy at birth for any population usually reflects very high rates of infant mortality. That’s a measure of deaths in the first year of life. Given that life expectancies reflect averages for a population, a high number of deaths at very young ages will skew calculations of life expectancy at birth toward younger ages. But typically, many people in those populations who make it past the vulnerable infant and early childhood years can expect to live relatively long lives.
Advances in modern sanitation – which reduce the spread of diarrheal diseases that are a major killer of infants – and vaccinations can greatly increase life expectancies.
Consider the effect of infant mortality on overall age patterns in two contemporary populations with dramatically different life expectancies at birth.
In Afghanistan, life expectancy at birth is low, at just over 53 years, and infant mortality is high, at almost 105 deaths for every 1,000 children born.
In Singapore, life expectancy at birth is much higher, at over 86 years, and infant mortality is very low – fewer than two infants die for every 1,000 who are born. In both countries, people do survive to very old ages. But in Afghanistan, because so many more people die at very young ages, proportionally fewer people survive to old age.
Living a long life has long been possible
It’s incorrect to view long lives as a remarkable and unique characteristic of the “modern” era.
Knowing that people often did have long lives in the past might help you feel more connected with the past. For example, you can imagine multigenerational households and gatherings, with grandparents in Neolithic China or Medieval England bouncing their grandchildren on their knees and telling them stories about their own childhoods decades before. You might have more in common with people who lived long ago than you had realized.
___
Sharon DeWitte receives funding from the National Science Foundation.
___
6 methods scientists are exploring to slow aging
Jacob Lund // Shutterstock
Aging is one of the most significant risk factors for many diseases, including cancers and neurodegenerative disorders like Alzheimer’s—and the older a person is, the more likely they are to have multiple chronic illnesses.
Diet and lifestyle choices are key ways to live longer; however, our family history can also play a role. “Our genes could get most of us close to the remarkable age of 90 if we lead a healthy lifestyle,” said Dr. Thomas Perls, an expert on aging and director at the Boston University School of Medicine.
While longevity is directly related to one’s health behaviors, scientists studying regeneration and aging have advanced our knowledge of how our bodies change over time. With this in mind, Guava Health compiled a list of six developing scientific research areas aimed at slowing aging. While researchers have yet to find the proverbial fountain of youth, their discoveries have given more insight on the science behind aging.
Jacob Lund // Shutterstock
Aging is one of the most significant risk factors for many diseases, including cancers and neurodegenerative disorders like Alzheimer’s—and the older a person is, the more likely they are to have multiple chronic illnesses.
Diet and lifestyle choices are key ways to live longer; however, our family history can also play a role. “Our genes could get most of us close to the remarkable age of 90 if we lead a healthy lifestyle,” said Dr. Thomas Perls, an expert on aging and director at the Boston University School of Medicine.
While longevity is directly related to one’s health behaviors, scientists studying regeneration and aging have advanced our knowledge of how our bodies change over time. With this in mind, Guava Health compiled a list of six developing scientific research areas aimed at slowing aging. While researchers have yet to find the proverbial fountain of youth, their discoveries have given more insight on the science behind aging.
There has been a surge in popularity for fasting, which ranks among Google’s top-trending diet searches. By restricting how much or how often you eat, intermittent fasting aims to regulate the body’s metabolism. But could it also be an anti-aging weapon?
The health benefits of intermittent fasting are well established in animals, with recent studies showing promising results for humans as well. However, it is not clear if this will lead to similar lifespan effects or whether there is also a certain type (or combination) of food that must be consumed during these periods. Animal testing has shown mixed responses regarding its effectiveness on weight loss, and human trials have not yet proven to be effective long term. Intermittent fasting works by metabolic switching, in which fasting triggers the body to switch its source of energy from glucose stored in the liver to ketones, a substance produced when your cells are low in glucose.
Dr. Richard J. Hodes, director of the National Institute on Aging, said a study effectively demonstrated that when mice eat one meal per day and had the longest fasting period, they seemed to have a longer lifespan and better outcomes for common age-related liver disease and metabolic disorders.
Researchers continue to expand on these findings in lab studies, and many are hopeful there may be potential anti-aging benefits for humans including reducing age-related metabolic disorders.
New Africa // Shutterstock
There has been a surge in popularity for fasting, which ranks among Google’s top-trending diet searches. By restricting how much or how often you eat, intermittent fasting aims to regulate the body’s metabolism. But could it also be an anti-aging weapon?
The health benefits of intermittent fasting are well established in animals, with recent studies showing promising results for humans as well. However, it is not clear if this will lead to similar lifespan effects or whether there is also a certain type (or combination) of food that must be consumed during these periods. Animal testing has shown mixed responses regarding its effectiveness on weight loss, and human trials have not yet proven to be effective long term. Intermittent fasting works by metabolic switching, in which fasting triggers the body to switch its source of energy from glucose stored in the liver to ketones, a substance produced when your cells are low in glucose.
Dr. Richard J. Hodes, director of the National Institute on Aging, said a study effectively demonstrated that when mice eat one meal per day and had the longest fasting period, they seemed to have a longer lifespan and better outcomes for common age-related liver disease and metabolic disorders.
Researchers continue to expand on these findings in lab studies, and many are hopeful there may be potential anti-aging benefits for humans including reducing age-related metabolic disorders.
As we age, our immune systems can progressively diminish over time. An important goal of aging research is to develop strategies to stimulate the immune system so our bodies stay resilient and less susceptible to diseases.
Experimental combination therapy of two anti-aging compounds, known as “mechanistic target of rapamycin,” or mTOR inhibitors, has been shown to extend the lifespan of and revitalize the aging immune system and organs of mice.
In a 2018 clinical trial funded by pharmaceutical company Novartis, 264 volunteers 65 and older received one or both of the drugs, or were assigned to a control group with placebos. Those who had taken low doses of both drugs reported 1.49 respiratory infections over one year on average, versus 2.41 in the placebo group.
The immune system can play a big role in alleviating many anticipated physical ailments. Its ability to regulate homeostasis and fight infection makes it an area of interest for scientists who seek to combat aging processes ranging from wrinkles to cancer. Their research includes therapies focusing on replenishing aged immune system tissues or cells, immunosuppressive strategies, and various approaches that target specific cell types.
smolaw // Shutterstock
As we age, our immune systems can progressively diminish over time. An important goal of aging research is to develop strategies to stimulate the immune system so our bodies stay resilient and less susceptible to diseases.
Experimental combination therapy of two anti-aging compounds, known as “mechanistic target of rapamycin,” or mTOR inhibitors, has been shown to extend the lifespan of and revitalize the aging immune system and organs of mice.
In a 2018 clinical trial funded by pharmaceutical company Novartis, 264 volunteers 65 and older received one or both of the drugs, or were assigned to a control group with placebos. Those who had taken low doses of both drugs reported 1.49 respiratory infections over one year on average, versus 2.41 in the placebo group.
The immune system can play a big role in alleviating many anticipated physical ailments. Its ability to regulate homeostasis and fight infection makes it an area of interest for scientists who seek to combat aging processes ranging from wrinkles to cancer. Their research includes therapies focusing on replenishing aged immune system tissues or cells, immunosuppressive strategies, and various approaches that target specific cell types.
As we get older, our cells also age and become less functional. Cellular senescence is a process in which cells lose the ability to divide and replicate. Senescent cells are resistant to cell death, so they’re often known as “zombie cells.” They can no longer serve a function and cause damage to neighboring cells.
A build-up of these zombie cells is a hallmark of aging linked to the deterioration of body organs and tissues and the development of age-related diseases. In lab tests, removing these cells can improve tissue function. While the precise role of senescent cells in aging is still not fully understood, they play a significant role in the body’s degenerative changes that occur over time.
Senolytics are a class of drugs that selectively eliminate senescent cells, which may help to slow the aging process. In 2016, two separate research groups published findings on the discovery of new senolytic drugs, which selectively kill senescent cells. Studies led by the University of Arkansas showed the drug ABT-263 (Navitoclax) could selectively kill senescent cells and make tissue young again. Scientists from the Weizmann Institute of Science in Israel used a similar drug, ABT-737, to kill senescent cells in the lungs and skin of mice.
In a 2018 study led by Mayo Clinic researcher James Kirkland tested a combination of dasatinib, used to treat some forms of leukemia, and quercetin, a plant flavanol found in some fruits and vegetables. The drug combination was tested in aging mice to see whether it could slow physical dysfunction caused by senescent cells. It was shown to be effective, suggesting that future studies could find compounds like this that are effective in humans.
totojang1977 // Shutterstock
As we get older, our cells also age and become less functional. Cellular senescence is a process in which cells lose the ability to divide and replicate. Senescent cells are resistant to cell death, so they’re often known as “zombie cells.” They can no longer serve a function and cause damage to neighboring cells.
A build-up of these zombie cells is a hallmark of aging linked to the deterioration of body organs and tissues and the development of age-related diseases. In lab tests, removing these cells can improve tissue function. While the precise role of senescent cells in aging is still not fully understood, they play a significant role in the body’s degenerative changes that occur over time.
Senolytics are a class of drugs that selectively eliminate senescent cells, which may help to slow the aging process. In 2016, two separate research groups published findings on the discovery of new senolytic drugs, which selectively kill senescent cells. Studies led by the University of Arkansas showed the drug ABT-263 (Navitoclax) could selectively kill senescent cells and make tissue young again. Scientists from the Weizmann Institute of Science in Israel used a similar drug, ABT-737, to kill senescent cells in the lungs and skin of mice.
In a 2018 study led by Mayo Clinic researcher James Kirkland tested a combination of dasatinib, used to treat some forms of leukemia, and quercetin, a plant flavanol found in some fruits and vegetables. The drug combination was tested in aging mice to see whether it could slow physical dysfunction caused by senescent cells. It was shown to be effective, suggesting that future studies could find compounds like this that are effective in humans.
The U.S. Preventive Services Task Force recommends that women aged 65 or older and those at risk for osteoporosis get regular bone measurement testing. Bones thin and weaken over time, increasing the risk of osteoporosis and making them more susceptible to fractures and breaks.
A 2014 study indicated that resveratrol, a natural phytoestrogen, could be a potential anti-aging therapy for bones. The research, which focused on bone mass and biomechanical properties in 20 rats, found resveratrol can increase bone microstructure and mechanical properties.
Interestingly, incorporating resveratrol into dietary supplements or foods has become a popular option for anti-aging, and reports suggest that resveratrol treatment may have beneficial effects, including slowing bone loss.
Canva
The U.S. Preventive Services Task Force recommends that women aged 65 or older and those at risk for osteoporosis get regular bone measurement testing. Bones thin and weaken over time, increasing the risk of osteoporosis and making them more susceptible to fractures and breaks.
A 2014 study indicated that resveratrol, a natural phytoestrogen, could be a potential anti-aging therapy for bones. The research, which focused on bone mass and biomechanical properties in 20 rats, found resveratrol can increase bone microstructure and mechanical properties.
Interestingly, incorporating resveratrol into dietary supplements or foods has become a popular option for anti-aging, and reports suggest that resveratrol treatment may have beneficial effects, including slowing bone loss.
The field of tissue engineering is an interdisciplinary study that aims to develop biological substitutes for maintaining or restoring function in damaged cells. Some examples of successful—but experimental and expensive—regenerative therapies include rebuilding supplemental bladders, small arteries, skin grafts, cartilage, and even a full trachea.
In the early 2000s, researchers faced challenges in organ transplantation, and alternative tissue and organ reconstruction emerged. It may be possible someday to isolate a patient’s cells via a small biopsy, expand the number of cells in culture, and implant them, giving researchers even more information about how to beat the effects of aging.
Alex_Traksel // Shutterstock
The field of tissue engineering is an interdisciplinary study that aims to develop biological substitutes for maintaining or restoring function in damaged cells. Some examples of successful—but experimental and expensive—regenerative therapies include rebuilding supplemental bladders, small arteries, skin grafts, cartilage, and even a full trachea.
In the early 2000s, researchers faced challenges in organ transplantation, and alternative tissue and organ reconstruction emerged. It may be possible someday to isolate a patient’s cells via a small biopsy, expand the number of cells in culture, and implant them, giving researchers even more information about how to beat the effects of aging.
The Institute of Zoology at the Chinese Academy of Sciences discovered a method involving a gene called kat7, which could be a key contributor to cellular aging. The research found when the kat7 gene in mice was inactivated, or made inoperable, 25% of their lifespans increased, and their overall appearance and grip strength improved.
Stanford University continues to research Yamanaka factors, proteins known to turn mature cells into iPS cells, or induced pluripotent stem cells. iPS cells are foundational to regenerative research because they can grow and develop into any type of cell in the body. During this process, cells revert to a more vigorous state and shed any “memory” of previous identities while reverting to a younger state.
The Broad Stem Cell Research Center at UCLA proposes iPS cells can be used to create cancer-free cells for a leukemia patient or developed into neurons to treat neurological disorders.
This story originally appeared on Guava Health and was produced and distributed in partnership with Stacker Studio.
angellodeco // Shutterstock
The Institute of Zoology at the Chinese Academy of Sciences discovered a method involving a gene called kat7, which could be a key contributor to cellular aging. The research found when the kat7 gene in mice was inactivated, or made inoperable, 25% of their lifespans increased, and their overall appearance and grip strength improved.
Stanford University continues to research Yamanaka factors, proteins known to turn mature cells into iPS cells, or induced pluripotent stem cells. iPS cells are foundational to regenerative research because they can grow and develop into any type of cell in the body. During this process, cells revert to a more vigorous state and shed any “memory” of previous identities while reverting to a younger state.
The Broad Stem Cell Research Center at UCLA proposes iPS cells can be used to create cancer-free cells for a leukemia patient or developed into neurons to treat neurological disorders.
This story originally appeared on Guava Health and was produced and distributed in partnership with Stacker Studio.
A licensed and credentialed trainer can design a personalized program and teach you proper form and technique. Get referrals from local gyms, and many trainers now offer virtual workouts. After you learn the basics, you can work out on your own.
A licensed and credentialed trainer can design a personalized program and teach you proper form and technique. Get referrals from local gyms, and many trainers now offer virtual workouts. After you learn the basics, you can work out on your own.
Training with free weights, like dumbbells, kettlebells and barbells, is often better for muscle building than machines, Shawn Pedicini, a physical therapist at Harvard-affiliated Spaulding Rehabilitation Hospital, says. “However, machines are ideal if you have balancing issues or other limitations that make it safer to sit during weight training,” he says. You can also go back and forth between free weights and machines depending on the type of exercise and which muscles you are working on.
Training with free weights, like dumbbells, kettlebells and barbells, is often better for muscle building than machines, Shawn Pedicini, a physical therapist at Harvard-affiliated Spaulding Rehabilitation Hospital, says. “However, machines are ideal if you have balancing issues or other limitations that make it safer to sit during weight training,” he says. You can also go back and forth between free weights and machines depending on the type of exercise and which muscles you are working on.
While you need full-body workouts that address all your major muscles, older adults should pay special attention to their leg muscles: quadriceps and hamstrings (in the thighs), the gluteals (in the buttocks) and the calf muscles. “These are involved in many daily functional movements like squatting and climbing stairs,” Pedicini says. Compound exercises that work different muscles in one movement — like squats, deadlifts and lunges — are great for building leg muscles.
While you need full-body workouts that address all your major muscles, older adults should pay special attention to their leg muscles: quadriceps and hamstrings (in the thighs), the gluteals (in the buttocks) and the calf muscles. “These are involved in many daily functional movements like squatting and climbing stairs,” Pedicini says. Compound exercises that work different muscles in one movement — like squats, deadlifts and lunges — are great for building leg muscles.
Pedicini says fewer reps with heavier weights helps you gain the most muscle. “An ideal routine would be eight repetitions for each exercise for three sets total.” But you can adjust this as needed. “People with movement issues might need to use lighter weights and do more repetitions.”
Pedicini says fewer reps with heavier weights helps you gain the most muscle. “An ideal routine would be eight repetitions for each exercise for three sets total.” But you can adjust this as needed. “People with movement issues might need to use lighter weights and do more repetitions.”
Lifting should be done at a seven-second tempo. That means three seconds to lift the weight, a one-second pause and three seconds to lower it. If you can’t lift the weight at least eight times, use a lighter weight. When you can comfortably perform eight reps without completely tiring the muscle, increase the weight. “Muscles grow stronger only if you keep adding resistance,” Pedicini says.
Lifting should be done at a seven-second tempo. That means three seconds to lift the weight, a one-second pause and three seconds to lower it. If you can’t lift the weight at least eight times, use a lighter weight. When you can comfortably perform eight reps without completely tiring the muscle, increase the weight. “Muscles grow stronger only if you keep adding resistance,” Pedicini says.
Ideally, you should do weight training at least twice a week. “Two days of full-body training can produce measurable changes in muscle strength,” Pedicini says. You often can feel results after four to six weeks of consistent training.
Ideally, you should do weight training at least twice a week. “Two days of full-body training can produce measurable changes in muscle strength,” Pedicini says. You often can feel results after four to six weeks of consistent training.
Always allow at least 48 hours between sessions for muscle recovery. Some people prefer to break their workouts into two parts: upper body and lower body. In that case, you can perform upper-body exercises one day and lower-body the next.
Always allow at least 48 hours between sessions for muscle recovery. Some people prefer to break their workouts into two parts: upper body and lower body. In that case, you can perform upper-body exercises one day and lower-body the next.
Use enough weight so that the last few reps of a lifting routine are challenging.
“Don’t forget to consistently challenge yourself as you progress,” Pedicini says. “It’s necessary to gain the muscle and strength changes you want and need.”
Use enough weight so that the last few reps of a lifting routine are challenging.
“Don’t forget to consistently challenge yourself as you progress,” Pedicini says. “It’s necessary to gain the muscle and strength changes you want and need.”