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Longitudinal associations between use of antihypertensive, antidiabetic, and lipid-lowering medications and biological aging
Aging is a major risk factor for many chronic diseases. This study aimed to examine the effects of antihypertensive, lipid-lowering, and antidiabetic drugs on biological aging. We included 672 participants and 2746 repeated measurements from the Swedish Adoption/Twin Study of Aging. Self-reported me...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400489/ https://www.ncbi.nlm.nih.gov/pubmed/37032369 http://dx.doi.org/10.1007/s11357-023-00784-8 |
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author | Tang, Bowen Li, Xia Wang, Yunzhang Sjölander, Arvid Johnell, Kristina Thambisetty, Madhav Ferrucci, Luigi Reynolds, Chandra A. Finkel, Deborah Jylhävä, Juulia Pedersen, Nancy L. Hägg, Sara |
author_facet | Tang, Bowen Li, Xia Wang, Yunzhang Sjölander, Arvid Johnell, Kristina Thambisetty, Madhav Ferrucci, Luigi Reynolds, Chandra A. Finkel, Deborah Jylhävä, Juulia Pedersen, Nancy L. Hägg, Sara |
author_sort | Tang, Bowen |
collection | PubMed |
description | Aging is a major risk factor for many chronic diseases. This study aimed to examine the effects of antihypertensive, lipid-lowering, and antidiabetic drugs on biological aging. We included 672 participants and 2746 repeated measurements from the Swedish Adoption/Twin Study of Aging. Self-reported medicine uses were categorized into antidiabetic, antihypertensive, and lipid-lowering drugs. A total of 12 biomarkers for biological aging (BA biomarkers) were included as outcomes. Conditional generalized estimating equations were applied conditioning on individuals to estimate the drug effect on BA biomarker level within the same person when using or not using the drug. Chronological age, body mass index, smoking status, number of multiple medication uses, blood pressure, blood glucose level, and apoB/apoA ratio were adjusted for as covariates in the model. Overall, using antihypertensive drugs was associated with a decrease in one DNA-methylation age (PCGrimAge: beta = − 0.39, 95%CI = − 0.67 to − 0.12). When looking into drug subcategories, calcium channel blockers (CCBs) were associated with a decrease in several DNA-methylation ages (PCHorvathAge beta = − 1.28, 95%CI = − 2.34 to − 0.21; PCSkin&bloodAge beta = − 1.34, 95%CI = − 2.61 to − 0.07; PCPhenoAge beta = − 1.74, 95%CI = − 2.58 to − 0.89; PCGrimAge beta = − 0.57, 95%CI = − 0.96 to − 0.17) and in functional biological ages (functional age index beta = − 2.18, 95%CI = − 3.65 to − 0.71; frailty index beta = − 1.31, 95%CI = − 2.43 to − 0.18). However, the results within other drug subcategories were inconsistent. Calcium channel blockers may decrease biological aging captured by the BA biomarkers measured at epigenetic and functional level. Future studies are warranted to confirm these effects and understand the underlying biological mechanisms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11357-023-00784-8. |
format | Online Article Text |
id | pubmed-10400489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-104004892023-08-05 Longitudinal associations between use of antihypertensive, antidiabetic, and lipid-lowering medications and biological aging Tang, Bowen Li, Xia Wang, Yunzhang Sjölander, Arvid Johnell, Kristina Thambisetty, Madhav Ferrucci, Luigi Reynolds, Chandra A. Finkel, Deborah Jylhävä, Juulia Pedersen, Nancy L. Hägg, Sara GeroScience Original Article Aging is a major risk factor for many chronic diseases. This study aimed to examine the effects of antihypertensive, lipid-lowering, and antidiabetic drugs on biological aging. We included 672 participants and 2746 repeated measurements from the Swedish Adoption/Twin Study of Aging. Self-reported medicine uses were categorized into antidiabetic, antihypertensive, and lipid-lowering drugs. A total of 12 biomarkers for biological aging (BA biomarkers) were included as outcomes. Conditional generalized estimating equations were applied conditioning on individuals to estimate the drug effect on BA biomarker level within the same person when using or not using the drug. Chronological age, body mass index, smoking status, number of multiple medication uses, blood pressure, blood glucose level, and apoB/apoA ratio were adjusted for as covariates in the model. Overall, using antihypertensive drugs was associated with a decrease in one DNA-methylation age (PCGrimAge: beta = − 0.39, 95%CI = − 0.67 to − 0.12). When looking into drug subcategories, calcium channel blockers (CCBs) were associated with a decrease in several DNA-methylation ages (PCHorvathAge beta = − 1.28, 95%CI = − 2.34 to − 0.21; PCSkin&bloodAge beta = − 1.34, 95%CI = − 2.61 to − 0.07; PCPhenoAge beta = − 1.74, 95%CI = − 2.58 to − 0.89; PCGrimAge beta = − 0.57, 95%CI = − 0.96 to − 0.17) and in functional biological ages (functional age index beta = − 2.18, 95%CI = − 3.65 to − 0.71; frailty index beta = − 1.31, 95%CI = − 2.43 to − 0.18). However, the results within other drug subcategories were inconsistent. Calcium channel blockers may decrease biological aging captured by the BA biomarkers measured at epigenetic and functional level. Future studies are warranted to confirm these effects and understand the underlying biological mechanisms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11357-023-00784-8. Springer International Publishing 2023-04-10 /pmc/articles/PMC10400489/ /pubmed/37032369 http://dx.doi.org/10.1007/s11357-023-00784-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Tang, Bowen Li, Xia Wang, Yunzhang Sjölander, Arvid Johnell, Kristina Thambisetty, Madhav Ferrucci, Luigi Reynolds, Chandra A. Finkel, Deborah Jylhävä, Juulia Pedersen, Nancy L. Hägg, Sara Longitudinal associations between use of antihypertensive, antidiabetic, and lipid-lowering medications and biological aging |
title | Longitudinal associations between use of antihypertensive, antidiabetic, and lipid-lowering medications and biological aging |
title_full | Longitudinal associations between use of antihypertensive, antidiabetic, and lipid-lowering medications and biological aging |
title_fullStr | Longitudinal associations between use of antihypertensive, antidiabetic, and lipid-lowering medications and biological aging |
title_full_unstemmed | Longitudinal associations between use of antihypertensive, antidiabetic, and lipid-lowering medications and biological aging |
title_short | Longitudinal associations between use of antihypertensive, antidiabetic, and lipid-lowering medications and biological aging |
title_sort | longitudinal associations between use of antihypertensive, antidiabetic, and lipid-lowering medications and biological aging |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400489/ https://www.ncbi.nlm.nih.gov/pubmed/37032369 http://dx.doi.org/10.1007/s11357-023-00784-8 |
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