Evidence map›Paper›PMID 41071644›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2026

Joint association of serum 25-hydroxyvitamin D concentration and body mass index on the acceleration of clinical biomarker-based biological aging.

Zimo Pan, Jing Zeng, Zeyu Chen, Shimin Chen, Junhan Yang, Huaihao Li, Shengshu Wang, Jianhua Wang, Nan Li, Yanping Gong and 2 more

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Zimo PanDepartment of Endocrinology, the Second Medical Center & National Clinical Research Center for Geriatric Disease, Chinese PLA General Hospital, Beijing, China.
Jing ZengDepartment of Endocrinology, the Second Medical Center & National Clinical Research Center for Geriatric Disease, Chinese PLA General Hospital, Beijing, China.
Zeyu ChenSchool of Basic Medicine, Army Medical University, Chongqing, China.
Shimin ChenMedical School of Chinese PLA, Beijing, China.
Junhan YangMedical School of Chinese PLA, Beijing, China.
Huaihao LiMedical School of Chinese PLA, Beijing, China.
Shengshu WangInstitute of Geriatrics, Beijing Key Laboratory of Aging and Geriatrics, National Clinical Research Center for Geriatric Diseases, Second Medical Center, Chinese People's Liberation Army General Hospital, Beijing, China.
Jianhua WangInstitute of Geriatrics, Beijing Key Laboratory of Aging and Geriatrics, National Clinical Research Center for Geriatric Diseases, Second Medical Center, Chinese People's Liberation Army General Hospital, Beijing, China.
Nan LiDepartment of Endocrinology, the Second Medical Center & National Clinical Research Center for Geriatric Disease, Chinese PLA General Hospital, Beijing, China.
Yanping GongDepartment of Endocrinology, the Second Medical Center & National Clinical Research Center for Geriatric Disease, Chinese PLA General Hospital, Beijing, China.
Miao LiuNational Key Laboratory of Kidney Disease, Chinese PLA General Hospital, Beijing, China.
Chunlin LiDepartment of Endocrinology, the Second Medical Center & National Clinical Research Center for Geriatric Disease, Chinese PLA General Hospital, Beijing, China.

Funding

National Clinical Research Center for Geriatric Diseases, Chinese PLA General Hospital NCRCG-PLAGH-2023001National Key Research and Development Program of China 2022YFC2503605National Natural Science Foundation of China 82173589
6 · The paper itself

Abstract

backgroundThe possible joint association of vitamin D and obesity in regard to clinical biomarker-based biological aging process has not been well studied. We investigated the independent and combined associations of serum 25-hydroxyvitamin D [25(OH)D] concentrations and body mass index (BMI) with phenotypic age (PhenoAge) and Klemera-Doubal method Biological Age (KDM-BA) acceleration.

methodsThis study was conducted using data from participants in the UK Biobank baseline survey. Restricted cubic splines and multivariable logistic regression analyses were used to investigate the associations of serum 25(OH)D concentrations and BMI with PhenoAge and KDM-BA acceleration. Mediation analyses were conducted to assess whether biological age acceleration potentially mediated the association between 25(OH)D or BMI and all-cause mortality.

resultsIn Analysis 1 (n = 389 217) for PhenoAge, and Analysis 2 for KDM-BA (n = 329 561), participants whose serum 25(OH)D concentration ≥50.0 nmol/L or with normal weight (BMI <25 kg/m2) had the lowest odds of biological age acceleration. Those with both 25(OH)D <25.0 nmol/L and BMI ≥30.0 kg/m2 had the highest odds of PhenoAge acceleration ([OR [95% CI], 2.387 [2.303, 2.474]) and KDM-BA acceleration [OR (95% CI), 4.096 (3.926, 4.274)]. The mediation analysis revealed that PhenoAge acceleration mediated 11.4% and 47.1% of the associations of 25(OH)D and BMI with all-cause mortality; while KDM-BA acceleration accounted for 7.41% and 55.2%.

conclusionsSerum 25(OH)D concentrations and BMI were significantly associated with the acceleration of biological aging. Combining vitamin D deficiency and obesity demonstrated enhanced synergistic association on the biological aging process, highlighting the importance of vitamin D and BMI in promoting healthy aging.

Indexed as

AgingBody Mass IndexObesityVitamin DAgedAged, 80 and overBiomarkersFemaleHumansMaleMiddle AgedUnited Kingdom25-hydroxyvitamin DBiomarkersVitamin DBiological ageObesityPhenoAgeUK biobankVitamin D

Identifiers

PMID41071644
PMCPMC12758972

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.