매일 종합 비타민제를 사용하면 생물학적 노화가 느려질 수 있습니다: COSMOS 실험 결과

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원문 출처: hackernews · Genesis Park에서 요약 및 분석

요약

매사추세츠 브리겸 연구진이 COSMOS 임상시험 데이터를 분석한 결과, 65세 이상 성인이 2년간 매일 멀티비타민을 섭취하면 생물학적 노화가 평균 4개월가량 지연된다는 사실이 밝혀졌습니다. 연구진은 혈액 샘플의 DNA 메틸화를 분석하여 5가지 에피지네틱 시계에서 모두 노화 속도 둔화 효과를 확인했으며, 특히 실제 나이보다 생물학적 나이가 많은 참가자에게서 더 큰 효과가 나타났습니다. 이번 연구는 멀티비타민 복용이 단순한 수명 연장뿐만 아니라 삶의 질을 높이는 건강한 노화를 유도하는 안전하고 접근 가능한 방법이 될 수 있음을 시사합니다.

본문

An analysis led by Mass General Brigham investigators found slower aging in older adults after two years of a daily multivitamin, with greater benefits for those who began the trial with accelerated biological age. How quickly our bodies age on a cellular level, our “biological age,” can differ from how old we actually are in years. Using data from a large randomized clinical trial of older adults, researchers at Mass General Brigham evaluated the effects of taking a daily multivitamin over the course of two years on five measures of biological aging and found a slowing equivalent to about four months of aging. The benefits were increased in those who were biologically older than their actual age at the start of the trial. Their results are published in Nature Medicine. “There is a lot of interest today in identifying ways to not just live longer, but to live better,” said senior author Howard Sesso, ScD, MPH, associate director of the Division of Preventive Medicine in the Mass General Brigham Department of Medicine. “It was exciting to see the benefits of a multivitamin linked with markers of biological aging. This study opens the door to learning more about accessible, safe interventions that contribute to healthier, higher-quality aging.” Epigenetic clocks estimate biological aging based on tiny changes in our DNA. These clocks look at specific sites in our DNA that regulate gene expression (known as DNA methylation) and change naturally as we get older, helping track mortality and the pace of aging. This study, which uses data from the well-established COcoa Supplement Multivitamins Outcomes Study (COSMOS), analyzed DNA methylation data from blood samples of 958 randomly selected healthy participants with an average chronological age of 70. The study participants were randomized to take a daily cocoa extract and multivitamin; daily cocoa extract and placebo; placebo and multivitamin; or placebos only. Samples were analyzed for changes in five epigenetic clocks from the start of the trial and at the end of the first and second years. Compared to the placebo only group, people in the multivitamin group had slowing in all five epigenetic clocks, including statistically significant slowing seen in the two clocks that are predictive of mortality. The changes equated to about four months less biological aging over the course of two years. Additionally, people who were biologically older than their actual age at the start of the trial benefited the most. “We plan to do follow-up research to determine if the slowing of biological aging—observed through these five epigenetic clocks, and additional or new ones—persists after the trial ends,” said co-author and collaborator Yanbin Dong, MD, PhD, director of Georgia Prention Institute, Medical College of Georgia at Augusta Univeristy. Further studies are also needed to determine how improvements in biological aging may explain reductions in clinical outcomes. The COSMOS team plans to investigate how the effects of a daily multivitamin on biological aging may extend to different outcomes they have seen evidence of benefits for, such as improvements in cognition and reductions in cancer and cataracts. “A lot of people take a multivitamin without necessarily knowing any benefits from taking it, so the more we can learn about its potential health benefits, the better,” said Sesso. “Within COSMOS, we are fortunate and excited to build upon a rich resource of biomarker data to test how two interventions may improve biological aging and reduce age-related clinical outcomes.” Authorship: In addition to Sesso, Mass General Brigham authors include Sidong Li, Rikuta Hamaya, Alexandre C. Pereira, Kerry L. Ivey, Pamela M. Rist, and JoAnn E. Manson. Additional authors include Haidong Zhu, and Brian H. Chen. Disclosures: Manson and Sesso received investigator-initiated grants from Mars Edge, a segment of Mars Incorporated dedicated to nutrition research and products, for infrastructure support and donation of COSMOS study pills and packaging, and Pfizer Consumer Healthcare (now Haleon) for donation of COSMOS study pills (Centrum Silver and placebo) and packaging during the conduct of the study. Sesso additionally reported receiving investigator-initiated grants from Haleon, FOXO Technologies, Massachusetts Life Sciences Center, Pure Encapsulations, and American Pistachio Growers, and honoraria and/or travel for lectures from the Council for Responsible Nutrition, BASF, Haleon, and NIH during the conduct of the study. Rist has received in-kind support (specifically donations of study pills and packaging) from Mars Edge to be used in an NIH-funded, investigator-initiated trial (U01 AT012611). Chen was formerly an employee of FOXO Technologies, who provided in-kind donations to generate and pre-process the DNA methylation data. Charitable donations made possible by Sutter Health's California Pacific Medical Center Foundation provided salary support for Chen. Li received the EPI Ear

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