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Longevity Genes: Hacking healthspan using genomics

Key takeaways:
~ Researchers are actively trying to figure out how and why we age and why some people live longer without health problems.
~ About 25% of the variation in lifespan is due to genetic variants.
~ There are also genetic variants linked to a longer healthspan.

Understanding the genes linked to healthspan shows which pathways are actually important. The Lifehacks section includes research-backed ways to mimic the effect of ‘good’ longevity genes.

Members will see their genotype report below, plus additional solutions in the Lifehacks section. Consider joining today

Longevity: Living a long and healthy life

The average lifespan in the US is around 80. We generally accept it as ‘just the way it is’.

But… some people live to 100+ and are still relatively healthy. A few people live to 110 or 120.

When you look at the animal kingdom, most lab mice and rats live for 2 to 3 years. It is in line with other small mammals — except for the naked mole rat, which lives over 30 years in captivity without any age-related declines.[ref]

What is the difference? Why do some people live 20 or 30 years longer without dying of the chronic diseases of aging (heart disease, diabetes, cancer, Alzheimer’s)?

You may immediately assume that everyone who lives longer did everything right- exercised, meditated, ate the very best diet, etc. – but that isn’t necessarily the case. Researchers estimate that about 25% of the variation in lifespan is due to genetics.[ref]

What does it take to live a long, healthy life? Avoiding smoking, not drinking too much alcohol, and not getting cancer are important for the first 80 years. Beyond that, genetics becomes really important.

Looking at the genetic variants in long-lived humans as well as investigating long-lived animals, like the naked mole-rat, helps us understand what is important for extending healthspan and lifespan.

What can genetics tell us about longevity?

There are several ways to approach health problems:

  1. Mitigate the symptoms (take a pill that causes the symptom to go away, the way many doctors treat health issues today)
  2. Figure out what causes the symptoms on a population-wide level (e.g. epidemiological studies that show excessive soda consumption linked to metabolic syndrome)
  3. Try to determine the ‘root cause’ by looking at various metabolic pathways (for example, a deficiency in vitamin B12 is one cause of peripheral neuropathy)
  4. Study the genetic variants in people with a condition to see which genetic variants cause the problem:
    • focus on known genetic variants that researchers suspect should cause the condition
    • investigate the interaction between specific genetic variants and environmental conditions
    • look at the whole genome of a large population group to see if people with a certain condition have statistically different levels of a genetic variant

Researchers have used all of these methods to treat the diseases of aging. But the most exciting new research comes from looking at the genetic variants that cause the ‘condition’ of longevity.

The outliers, the centenarians living to 100, come from all types of backgrounds – different lifestyles, different ways of eating, different environmental factors. It makes epidemiological studies difficult.

However, centenarians have common genetic variants that can be determined with a whole lot of computing power. Longevity genes come to light with genome-wide association studies that look at vast amounts of genetic data.

Putting longevity statistics into perspective:

Before we get into the genetic variants that cause a statistical increase in the likelihood of living longer, let’s take a quick look at the baseline numbers.

Someone born a hundred years ago has less than a 1% chance of being alive today. In contrast, if you are a female born in 1973, your odds of living to 100 are 20%.

Chart from ‘What are the Odds‘ website.

 

Keep in mind, though, that these statistics are about the population in general rather than you as an individual. While genetics does play a role in how long you live, many other health, environmental, and lifestyle factors are also important.

Causes of mortality:

Understanding what causes most deaths can also guide us, to some extent, in our understanding of longevity.

In 2018, there were 2.8 million deaths in the US. The ten leading causes of death in the US are heart disease, cancer, unintentional injuries, lower respiratory diseases, stroke, Alzheimer’s, diabetes, influenza and pneumonia, kidney disease, and suicide.[ref]

What needs to go on at a cellular level for healthy aging?

Studies of centenarians show that their offspring also tend to live longer than their peers – and also have fewer of the diseases of aging. These studies also show that there isn’t just one thing, or a couple of things, that are different for centenarians. Instead, there is a lot of heterogeneity, small differences that affect many different aspects of health.[ref]

Let’s take a look at some of the causes of aging:

Cells accumulate damage and get replaced all the time, at all ages. It is just part of the way that the body works. The cells in your intestines turn over fairly quickly, with a cellular turnover rate of 2-6 days. Fat cells turnover every eight years. In contrast, most brain cells and heart cells are never replaced.[ref][ref]

You don’t want too much cell death or out-of-control cellular growth. Cells dying, getting cleared out, and replaced need to all work in concert.

Avoiding cancer:
When cells divide, the DNA needs to be copied correctly for the newly created cells. Errors in the DNA copy mechanism occur, and if the errors aren’t corrected, that cell may need to go through apoptosis (cell death). DNA errors that occur in specific genes cause cancer… Avoiding cancer is important for longevity. As we age, the odds of DNA errors increase due to various insults such as toxins that cause oxidative stress in the cell.

Telomeres:
When DNA is replicated, the end of the DNA strand is not included in the new cell. To compensate for this, at the end of each chromosome is a region of repeated nucleotides called the telomere. It protects the genes from getting cut off during replication. As cells replicate multiple times, the telomeres shorten, eventually getting too short and halting cell division. At this point, the cell goes into senescence and eventually cell death.

Telomere shortening isn’t as straightforward, though, as ‘replicate x number of times and stop’. Telomeres can lengthen again with the telomerase enzyme, coded for by the TERT gene. Both internal and external stress (toxin exposure) can decrease telomerase.

While it sounds like telomerase is the key to immortality (and it is for some cancer cell lines), telomerase is almost non-existent in certain body tissues, including the kidneys, blood vessels, liver, skin, and peripheral leukocytes. Genetic variants in the TERT gene (not covered by 23andMe or Ancestry) were recently linked to human longevity.[ref] (Note how well these tissues correspond well to the causes of mortality – cardiovascular disease, kidney disease, immune function).

Metabolism:
One way to increase lifespan in lab animals is to decrease calories.

Restricting calories works great for short-lived animals, but it doesn’t seem to be all that effective for humans and other long-lived mammals. But, this does point to metabolism being intertwined with longevity in some ways. A couple of the theoretical reasons for why calorie restriction increases lifespan include changes to IGF1 (insulin-like growth factor 1) and autophagy.[ref]

IGF1 (insulin-like growth factor 1) synthesizes in the liver. The level of growth hormone in the body is one of the main regulators, causing the liver to increase or decrease IGF1 production. IGF1 binds to its receptor on cell membranes throughout different tissues in the body. This binding activates many different actions to happen inside of a cell that are mostly related to being pro-growth. Lower levels of IGF1 are linked with extended lifespan in a lot of species, but there is a big tradeoff, at least in humans…IGF1 is really important for cognitive function and brain plasticity.[ref]

Longevity and lifespan are often about tradeoffs — those things that are beneficial for initial growth and development can become problematic later in life. IGF1 epitomizes this concept of tradeoffs, at least to some degree.

Autophagy:
Autophagy is the cellular cleaning up of damaged organelles and recycling of cellular waste. It is also important for targeting intracellular microbes and misfolded proteins.[ref]

Alzheimer’s:
Genetic variants in the APOE gene which increase the risk of Alzheimer’s also decrease longevity due to death from Alzheimer’s.

Excessive inflammatory response:
Inflammation is essential for fighting off a bacterial infection when you get a cut. But the flip side of the inflammatory response is that increased inflammation is linked to many chronic diseases, including cardiovascular disease, diabetes, and bone fragility. Elevated levels of inflammatory cytokines such as IL-6 are linked with decreased longevity.[ref]

Response to toxins:
Genetic variants influence how environmental toxins impact a person. Some of us are more resilient and can easily metabolize and get rid of various toxicants. Others may have a variant negatively impacting a detoxification pathway for a certain toxicant — which only matters if the person becomes exposed to that substance.

Genetics research shows links between CYP2B6 variants and longevity. The CYP2B6 enzyme is important in the metabolism of many drugs (including statins) as well as pesticides and insecticides (pyrethroids and DEET). Interestingly, women have higher CYP2B6 levels than men. It could also be that people with altered drug metabolism are statistically more likely to survive cancer and thus influence longevity statistics.[ref][ref]

Overall, genetics research shows that the following pathways are important for longevity:

  • apoptosis and autophagy
  • nutrient sensing and metabolism
  • tumor suppression
  • regulating growth
  • heart health
  • metabolism of xenobiotics

Next, let’s get into the variants you can check for with your genetic data.


Longevity Genotype Report:

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~ You'll see your genetic data in the articles and reports.

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Lifehacks: Diet, natural supplements, and lifestyle changes for longevity

While we can’t (yet) be like naked-mole rats, there are ways of influencing the genetic pathways linked with longevity.

Important here is not whether you carry the genetic variants linked to longevity, but instead, knowing which biological systems to target for healthspan.

Diets that increase FOXO3 and/or decrease IGF1:

Member Content:

  Log In


Why join Genetic Lifehacks?

~ Membership supports Genetic Lifehack's goal of explaining the latest health and genetics research.
~ It gives you access to the full article, including the Genotype and Lifehacks sections.
~ You'll see your genetic data in the articles and reports.

Join Here


Related Articles and Topics:

Telomere Length: How your genes affect telomeres and aging
Telomeres are the region of repeated nucleotides (the A, G, and T’s) that are found on the ends of all of your chromosomes. They cap off the end of the chromosomes, protecting the nuclear DNA during replication before cell division. Each time a cell divides, it makes a copy of the nuclear DNA and a little bit of the telomere is lost. When DNA replicates, it can’t replicate the very end part of the chromosome, where the telomere is located.

Klotho Gene: Anti-aging superpowers?
I’ve been fascinated by the Klotho gene for a while now, partly because it has a cool name. It is named after one of the Three Fates in Greek mythology who spin the thread of Life. Klotho (or Clotho) was responsible for the thread of life for all mortals, when they were born and when they died. As you will see, this is an aptly named gene that is intertwined with lifespan.

Top 10 Genes to Check in Your Genetic Raw Data
Wondering what is actually important in your genetic data? These 10 genes have important variants with a big impact on health. Check your genes (free article).

 

Originally published: Mar 2015. Revised and updated: August 2021.

References:

Albani, Diego, et al. “Insulin-like Growth Factor 1 Receptor Polymorphism Rs2229765 and Circulating Interleukin-6 Level Affect Male Longevity in a Population-Based Prospective Study (Treviso Longeva–TRELONG).” The Aging Male: The Official Journal of the International Society for the Study of the Aging Male, vol. 14, no. 4, Dec. 2011, pp. 257–64. PubMed, https://doi.org/10.3109/13685538.2011.607521.

Bojesen, Stig E., and Børge G. Nordestgaard. “The Common Germline Arg72Pro Polymorphism of P53 and Increased Longevity in Humans.” Cell Cycle (Georgetown, Tex.), vol. 7, no. 2, Jan. 2008, pp. 158–63. PubMed, https://doi.org/10.4161/cc.7.2.5249.

Bonafè, M., et al. “A Gender–Dependent Genetic Predisposition to Produce High Levels of IL-6 Is Detrimental for Longevity.” European Journal of Immunology, vol. 31, no. 8, Aug. 2001, pp. 2357–61. PubMed, https://doi.org/10.1002/1521-4141(200108)31:8<2357::aid-immu2357>3.0.co;2-x.

Crocco, Paolina, et al. “Inter-Individual Variability in Xenobiotic-Metabolizing Enzymes: Implications for Human Aging and Longevity.” Genes, vol. 10, no. 5, May 2019, p. 403. PubMed Central, https://doi.org/10.3390/genes10050403.

—. “Inter-Individual Variability in Xenobiotic-Metabolizing Enzymes: Implications for Human Aging and Longevity.” Genes, vol. 10, no. 5, May 2019, p. 403. PubMed Central, https://doi.org/10.3390/genes10050403.

CYP2B6 Cytochrome P450 Family 2 Subfamily B Member 6 [Homo Sapiens (Human)] – Gene – NCBI. https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=1555. Accessed 5 Jan. 2022.

Dato, Serena, et al. “Untangling the Genetics of Human Longevity—A Challenging Quest.” Genes, vol. 10, no. 8, July 2019, p. 585. PubMed Central, https://doi.org/10.3390/genes10080585.

De Rango, Francesco, et al. “Inositol Polyphosphate Multikinase (IPMK), a Gene Coding for a Potential Moonlighting Protein, Contributes to Human Female Longevity.” Genes, vol. 10, no. 2, Feb. 2019, p. 125. PubMed Central, https://doi.org/10.3390/genes10020125.

Di Bona, Danilo, et al. “Association between Genetic Variations in the Insulin/Insulin-like Growth Factor (Igf-1) Signaling Pathway and Longevity: A Systematic Review and Meta-Analysis.” Current Vascular Pharmacology, vol. 12, no. 5, 2014, pp. 674–81. PubMed, https://doi.org/10.2174/1570161111666131218152807.

Ferrucci, Luigi, and Elisa Fabbri. “Inflammageing: Chronic Inflammation in Ageing, Cardiovascular Disease, and Frailty.” Nature Reviews. Cardiology, vol. 15, no. 9, Sept. 2018, pp. 505–22. PubMed Central, https://doi.org/10.1038/s41569-018-0064-2.

Flachsbart, Friederike, et al. “Association of FOXO3A Variation with Human Longevity Confirmed in German Centenarians.” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 8, Feb. 2009, pp. 2700–05. PubMed Central, https://doi.org/10.1073/pnas.0809594106.

Grossi, Valentina, et al. “The Longevity SNP Rs2802292 Uncovered: HSF1 Activates Stress-Dependent Expression of FOXO3 through an Intronic Enhancer.” Nucleic Acids Research, vol. 46, no. 11, June 2018, pp. 5587–600. PubMed, https://doi.org/10.1093/nar/gky331.

Is Longevity Determined by Genetics?: MedlinePlus Genetics. https://medlineplus.gov/genetics/understanding/traits/longevity/. Accessed 5 Jan. 2022.

Levine, Beth, and Guido Kroemer. “Biological Functions of Autophagy Genes: A Disease Perspective.” Cell, vol. 176, no. 1–2, Jan. 2019, pp. 11–42. PubMed Central, https://doi.org/10.1016/j.cell.2018.09.048.

Li, Yuan, et al. “FoxO3a Regulates Inflammation-Induced Autophagy in Odontoblasts.” Journal of Endodontics, vol. 44, no. 5, May 2018, pp. 786–91. PubMed, https://doi.org/10.1016/j.joen.2017.12.023.

Mao, Yu-Qin, et al. “Longevity-Associated Forkhead Box O3 (FOXO3) Single Nucleotide Polymorphisms Are Associated with Type 2 Diabetes Mellitus in Chinese Elderly Women.” Medical Science Monitor: International Medical Journal of Experimental and Clinical Research, vol. 25, Apr. 2019, pp. 2966–75. PubMed, https://doi.org/10.12659/MSM.913788.

Masoro, Edward J. “Caloric Restriction-Induced Life Extension of Rats and Mice: A Critique of Proposed Mechanisms.” Biochimica et Biophysica Acta (BBA) – General Subjects, vol. 1790, no. 10, Oct. 2009, pp. 1040–48. ScienceDirect, https://doi.org/10.1016/j.bbagen.2009.02.011.

Nygaard, Marianne, et al. “AKT1 Fails to Replicate as a Longevity-Associated Gene in Danish and German Nonagenarians and Centenarians.” European Journal of Human Genetics: EJHG, vol. 21, no. 5, May 2013, pp. 574–77. PubMed, https://doi.org/10.1038/ejhg.2012.196.

Pawlikowska, Ludmila, et al. “Association of Common Genetic Variation in the Insulin/IGF1 Signaling Pathway with Human Longevity.” Aging Cell, vol. 8, no. 4, Aug. 2009, pp. 460–72. PubMed Central, https://doi.org/10.1111/j.1474-9726.2009.00493.x.

—. “Association of Common Genetic Variation in the Insulin/IGF1 Signaling Pathway with Human Longevity.” Aging Cell, vol. 8, no. 4, Aug. 2009, pp. 460–72. PubMed Central, https://doi.org/10.1111/j.1474-9726.2009.00493.x.

Philips, Ron Milo &. Ron. » How Quickly Do Different Cells in the Body Replace Themselves? http://book.bionumbers.org/how-quickly-do-different-cells-in-the-body-replace-themselves/. Accessed 5 Jan. 2022.

Products – Data Briefs – Number 355 – January 2020. 26 June 2020, https://www.cdc.gov/nchs/products/databriefs/db355.htm.

Ruby, J. Graham, et al. “Naked Mole-Rat Mortality Rates Defy Gompertzian Laws by Not Increasing with Age.” ELife, edited by Michael Rose, vol. 7, Jan. 2018, p. e31157. eLife, https://doi.org/10.7554/eLife.31157.

Sanders, Amy E., et al. “Association of a Functional Polymorphism in the Cholesteryl Ester Transfer Protein (CETP) Gene with Memory Decline and Incidence of Dementia.” JAMA, vol. 303, no. 2, Jan. 2010, pp. 150–58. PubMed, https://doi.org/10.1001/jama.2009.1988.

—. “Association of a Functional Polymorphism in the Cholesteryl Ester Transfer Protein (CETP) Gene with Memory Decline and Incidence of Dementia.” JAMA, vol. 303, no. 2, Jan. 2010, pp. 150–58. PubMed, https://doi.org/10.1001/jama.2009.1988.

Scarabino, Daniela, et al. “Analysis of the Association Between TERC and TERT Genetic Variation and Leukocyte Telomere Length and Human Lifespan—A Follow-Up Study.” Genes, vol. 10, no. 2, Jan. 2019, p. 82. PubMed Central, https://doi.org/10.3390/genes10020082.

Soerensen, Mette, et al. “No Association between Variation in Longevity Candidate Genes and Aging-Related Phenotypes in Oldest-Old Danes.” Experimental Gerontology, vol. 78, June 2016, pp. 57–61. PubMed, https://doi.org/10.1016/j.exger.2016.03.001.

What Are the Odds of Living to 100? https://discovertheodds.com/what-are-the-odds-of-living-to-100/. Accessed 5 Jan. 2022.

Williams, J. M., et al. “Epithelial Cell Shedding and Barrier Function.” Veterinary Pathology, vol. 52, no. 3, May 2015, pp. 445–55. PubMed Central, https://doi.org/10.1177/0300985814559404.

Wrigley, Sarah, et al. “Insulin-Like Growth Factor 1: At the Crossroads of Brain Development and Aging.” Frontiers in Cellular Neuroscience, vol. 11, Feb. 2017, p. 14. PubMed Central, https://doi.org/10.3389/fncel.2017.00014.

Zanger, Ulrich M., and Kathrin Klein. “Pharmacogenetics of Cytochrome P450 2B6 (CYP2B6): Advances on Polymorphisms, Mechanisms, and Clinical Relevance.” Frontiers in Genetics, vol. 4, Mar. 2013, p. 24. PubMed Central, https://doi.org/10.3389/fgene.2013.00024.

Zeng, Yi, et al. “Novel Loci and Pathways Significantly Associated with Longevity.” Scientific Reports, vol. 6, Feb. 2016, p. 21243. PubMed Central, https://doi.org/10.1038/srep21243.

Zhang, Yun-Xia, et al. “CETP Polymorphisms Confer Genetic Contribution to Centenarians of Hainan, South of China.” Asian Pacific Journal of Tropical Medicine, vol. 9, no. 9, Sept. 2016, pp. 872–76. PubMed, https://doi.org/10.1016/j.apjtm.2016.07.009.

https://academic.oup.com/nar/article/46/11/5587/4992648. Accessed 5 Jan. 2022.


About the Author:
Debbie Moon is the founder of Genetic Lifehacks. Fascinated by the connections between genes, diet, and health, her goal is to help you understand how to apply genetics to your diet and lifestyle decisions. Debbie has a BS in engineering from Colorado School of Mines and an MSc in biological sciences from Clemson University. Debbie combines an engineering mindset with a biological systems approach to help you understand how genetic differences impact your optimal health.