Evidence map›Paper›PMID 41193836›Full record

ArticleJournal of bone and mineral metabolism2026

Facial skin aging is a potential osteoporosis-associated marker: evidence from both observational and genetic studies.

Zhi-Dan Yu, Hai-Bei Zang, Yun-Jie Zhu, Xing-Hao Yu, Chang-Hua Tang, Han-Wen Cao, Xiao-Li Huang, Lin Bo, Shu-Feng Lei, Fei-Yan Deng

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Article in Journal of bone and mineral metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Zhi-Dan YuCollaborative Innovation Center for Bone and Immunology, Center for Genetic Epidemiology and Genomics, School of Public Health, Soochow University & Sihong Hospital, Suzhou Medical College of Soochow University, Suzhou, Jiangsu, 215123, People's Republic of China.
Hai-Bei ZangCollaborative Innovation Center for Bone and Immunology, Center for Genetic Epidemiology and Genomics, School of Public Health, Soochow University & Sihong Hospital, Suzhou Medical College of Soochow University, Suzhou, Jiangsu, 215123, People's Republic of China.
Yun-Jie ZhuCollaborative Innovation Center for Bone and Immunology, Center for Genetic Epidemiology and Genomics, School of Public Health, Soochow University & Sihong Hospital, Suzhou Medical College of Soochow University, Suzhou, Jiangsu, 215123, People's Republic of China.
Xing-Hao YuCollaborative Innovation Center for Bone and Immunology, Center for Genetic Epidemiology and Genomics, School of Public Health, Soochow University & Sihong Hospital, Suzhou Medical College of Soochow University, Suzhou, Jiangsu, 215123, People's Republic of China.
Chang-Hua TangDepartment of Orthopedics, Sihong Hospital, Sihong, Jiangsu, 223900, People's Republic of China.
Han-Wen CaoCollaborative Innovation Center for Bone and Immunology, Center for Genetic Epidemiology and Genomics, School of Public Health, Soochow University & Sihong Hospital, Suzhou Medical College of Soochow University, Suzhou, Jiangsu, 215123, People's Republic of China.
Xiao-Li HuangDepartment of Orthopedics, Sihong Hospital, Sihong, Jiangsu, 223900, People's Republic of China.
Lin BoDepartment of Rheumatology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, 215004, People's Republic of China.
Shu-Feng LeiCollaborative Innovation Center for Bone and Immunology, Center for Genetic Epidemiology and Genomics, School of Public Health, Soochow University & Sihong Hospital, Suzhou Medical College of Soochow University, Suzhou, Jiangsu, 215123, People's Republic of China. leisf@suda.edu.cn.ORCID http://orcid.org/0000-0002-7264-6869
Fei-Yan DengCollaborative Innovation Center for Bone and Immunology, Center for Genetic Epidemiology and Genomics, School of Public Health, Soochow University & Sihong Hospital, Suzhou Medical College of Soochow University, Suzhou, Jiangsu, 215123, People's Republic of China. fdeng@suda.edu.

Funding

Natural Science Foundation of China 82173529Natural Science Foundation of China 82173598Natural Science Foundation of China 82373587
6 · The paper itself

Abstract

introductionFacial skin aging (FSA) is a very easily observable indicator of aging, but whether FSA is associated with osteoporosis is still unknown. MATERIALS AND

methodsBased on the individual-level datasets from UK Biobank, this study calculated the PhenoAge (an accurate aging parameter), genetic risk score (GRS) and PhenoAge_advance, and performed multiple linear correlation analyses and Cox regression analyses. Based on the summary data from genome-wide association Studies (GWAS), linkage disequilibrium regression (LDSC), pleiotropic analysis under composite null hypothesis (PLACO) and Mendelian randomization (MR) analysis were performed to reveal shared genetic components and infer causal effects, respectively.

resultsHigher degrees of FSA were associated with lower eBMD (p < 0.001), and FSA was positively associated with the risks of osteoporosis (HR = 1.852, p < 0.001) and fracture (HR = 1.501, p < 0.001). However, FSA was not genetically associated as well as causally associated with all studied osteoporosis-related traits. In addition, we found significant phenotypic and genetic correlations between FSA and PhenoAge (rp = -0.137, p < 0.05) as well as between PhenoAge and fractures (rg = 0.092, p < 0.05).

conclusionFSA, PhenoAge and osteoporosis are three aging-related parameters that coexist with aging, and the aging process is accompanied by FSA and osteoporosis. FSA may serve as a marker for the onset of osteoporosis. These findings provide clues for early detection of bone loss in at-risk populations and for OP diagnosis using accurate clinical tools.

Indexed as

FaceOsteoporosisSkin AgingAgedBiomarkersBone DensityFemaleGenome-Wide Association StudyHumansMaleMendelian Randomization AnalysisMiddle AgedBiomarkersFacial skin agingGenetic Risk ScoreMendelian randomizationOsteoporosisPhenoAge

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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.