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The Vitamin-Lung Connection: New Research Ties A and D to Asthma Outcomes
In A Nutshell
- A study of more than 2,200 children and adults with asthma found that higher vitamin A and D levels were tied to better lung function and, in adults, to slower biological aging.
- Vitamin A was linked to better lung scores in both kids and adults, though one measure moved the opposite direction in children.
- A single gene called IRF5, along with 23 microRNAs, may help explain part of the connection between vitamin levels and lung and aging outcomes.
- The study is a single snapshot in time, so it shows a statistical link rather than proof that vitamins caused these effects.
More than 25 million Americans live with asthma, adjusting their days around inhalers, air quality alerts, and flare-ups. A large new study, published in Thorax, points to another factor that might also matter: vitamins A and D. Blood levels of both were tied to how well the lungs work, and in adults, to how fast the body ages at a cellular level.
In total, more than 2,200 children and adults with asthma took part in the study. Higher vitamin A levels lined up with better scores on some lung function tests in kids, though the picture wasn’t perfectly clean, since one measure moved the opposite way. In adults, higher levels of both vitamins tracked with stronger lung capacity, and those with enough vitamin D showed slower biological aging than those who were deficient.
This team didn’t stop at measuring vitamins and lung capacity. They also dug into the body’s molecular machinery, looking at gene-regulating molecules called microRNAs and chemical tags on DNA that can switch genes on or off, to get a sense of why vitamins might matter for lung health. In adults, statistical models suggested these molecular changes might partly explain the vitamin-lung and vitamin-aging links.
Vitamin A Tracked With Better Lung Capacity in Children and Adults
To get there, the team drew on two very different groups: 1,165 children with asthma, ages 6 to 14, followed through a long-running study in Costa Rica, and 1,041 adults with asthma, averaging 59 years old, from the Mass General Brigham Biobank. Everyone took a standard breathing test measuring how much air a person can forcefully blow out, and how fast. Blood samples supplied the vitamin readings, along with the microRNA and DNA data.
In kids, higher vitamin A tracked with better scores on two of the three lung measures: how much air they exhaled in one second, and the total amount of air they could forcefully blow out in one breath. It also tracked with a lower score on the ratio between those two numbers, so the results weren’t uniformly good news. Vitamin D showed no clear link to lung function in children, though vitamin D readings existed for only about half that group, which may explain the flat result rather than proving vitamin D truly doesn’t matter for kids’ lungs.
Vitamin D Sufficiency Linked to Slower Biological Aging
Biological age isn’t the number of candles on a birthday cake. Scientists have built tools called epigenetic clocks that estimate how fast a body is aging at the cellular level, based on chemical changes to DNA, and these clocks have proven better than chronological age at predicting mortality and other health outcomes.
Adults with vitamin D levels of 30 nanograms per milliliter or higher, the threshold doctors consider sufficient, scored better on several aging measures than adults who fell short. The gap between groups ranged from a few weeks to nearly four years of biological age, depending on which clock was used. Adults with weaker lungs also tended to test as biologically older across the board, reinforcing the idea that healthy lungs and slower aging go hand in hand.
One Gene, IRF5, Ties Vitamins to Lung and Aging Markers
A single gene called IRF5, which helps regulate inflammation and immune responses, has already been tied to asthma severity in earlier research, and it’s the most specific clue in this study. Higher levels of both vitamins were linked to a lighter dusting of chemical tags on one spot within that gene, in both children and adults. That same spot was statistically tied to lung function and to biological aging in adults, although the study’s own results and discussion sections describe the aging connection in ways that don’t fully agree, so exactly how that piece works is still unsettled. The team sees it as a promising lead worth chasing, not a settled mechanism.
Beyond that gene, the team flagged 23 microRNAs that statistically helped explain some of the vitamin-lung and vitamin-aging links in adults. The genes these microRNAs target point toward pathways involved in inflammation and cell growth, both of which play a role in asthma.
Findings Are Early and Not a Reason to Start Supplements
None of this means asthma patients should start popping vitamin pills. The study took a single snapshot of each person rather than tracking them over years, so it shows a statistical link, not proof that vitamins caused better lungs or slower aging. Vitamin A levels came from indirect blood markers rather than a direct measurement, adding some fuzziness, and the microRNA findings lean on outside databases rather than gene activity measured in these patients.
Even with those caveats, the authors say this is, to their knowledge, the first study to combine vitamin levels, lung function, and two kinds of molecular data in both children and adults with asthma. They are calling for future studies that track people’s vitamin levels over time.
For people living with asthma, the takeaway is more curiosity than prescription. Vitamins A and D look like more than a nutritional checkbox, statistically tied to markers of lung function and biological aging. Confirming whether that tie is more than coincidence will take years of tracking the same patients, not a single snapshot like this one.
Disclaimer: This article is for general informational purposes only and is not medical advice. Vitamin levels and their effects vary from person to person, and anyone with asthma should talk with a doctor before changing their diet, supplements, or treatment plan.
Paper Notes
Limitations
Study authors acknowledge several important constraints. Because data was collected at a single point in time rather than tracked longitudinally, the findings cannot establish that vitamins directly cause improvements in lung function or slower biological aging; only that the two are statistically associated. Vitamin A was measured using indirect metabolite markers from blood samples rather than direct, absolute quantification, which may introduce measurement imprecision. The study also lacked gene activity (mRNA expression) data, meaning the microRNA target findings are based on known relationships from existing databases rather than direct measurements within these cohorts. Authors also note that the absence of longitudinal data limits conclusions about how vitamin levels affect lung health over time.
Funding and Disclosures
This work was funded by the National Heart, Lung, and Blood Institute (NHLBI) under award numbers R01 HL139634 and R01 HL155742. The study was partially supported by TruDiagnostic for generating DNA methylation data for the adult cohort, under a Sponsored Research Agreement. Molecular data for the TOPMed program were supported by the NHLBI, with additional support noted for phenotype harmonization and data management. One author is listed as a Scientific Advisor to Antipode and TruDiagnostic, and receives funding from TruDiagnostic. Another author is a board member of Histolix and receives royalties from UpToDate. All other authors declared no conflicts of interest.
Publication Details
Paper Title: The impact of vitamins A and D on lung function and regulatory epigenetics in adult and childhood asthma | Authors: Rinku Sharma, Priyadarshini Kachroo, Kevin M. Mendez, Qingwen Chen, Julian Hecker, Sofina Begum, Rachel S. Kelly, Ryan Smith, Varun Dwaraka, Juan Carlos Celedon, Kelan G. Tantisira, Dawn L. DeMeo, Scott Weiss, Jessica Lasky-Su, Michael McGeachie | Institutions include: Department of Medicine, Brigham and Women’s Hospital, Boston, Massachusetts; Department of Health Informatics, Rutgers University Newark; TruDiagnostic LLC, Lexington, Kentucky; Pediatric Pulmonary Medicine, University of Pittsburgh; Department of Pediatrics, Division of Respiratory Medicine, University of California San Diego; Brigham and Women’s Hospital, Boston, Massachusetts | Journal: Thorax (BMJ Group), published online ahead of print June 30, 2026 | DOI: 10.1136/thorax-2025-223756







