Evidence map›Paper›PMID 42137350›Full record

ArticleFrontiers in endocrinology2026

Serum free and bioavailable rather than total testosterone is associated with the progression of non-alcoholic fatty liver disease in postmenopausal women: a prospective study.

Xu Wang, Qing Li, Jiesheng Lin, Zhijun Pan, Yupeng Zeng, Tianran Shen, Xu Chen, Wenhua Ling, Yuming Chen

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Article in Frontiers in endocrinology, 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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2 · The registry

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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

9 authors.

Xu WangDepartment of Clinical Nutrition, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China.
Qing LiGuangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, Guangdong, China.
Jiesheng LinGuangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, Guangdong, China.
Zhijun PanGuangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, Guangdong, China.
Yupeng ZengGuangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, Guangdong, China.
Tianran ShenGuangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, Guangdong, China.
Xu ChenGuangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, Guangdong, China.
Wenhua LingGuangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, Guangdong, China.
Yuming ChenGuangdong Provincial Key Laboratory of Food, Nutrition and Health, Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sex steroid hormones may play vital roles in predisposing individuals to metabolic diseases. However, relationship between testosterone and progression of non-alcoholic fatty liver disease (NAFLD) in postmenopausal women remains unclear. Therefore, we conducted a community-based prospective cohort study, to investigate the associations between NAFLD progression and serum testosterone, as well as its fractions, in postmenopausal women. Methods: A total of 1,705 postmenopausal women were included and analyzed after 5,269 person-years of follow-up. Serum total testosterone (TT) was measured by chemiluminescent immunoassay; concentrations and percentages (%) of free testosterone (cFT) and bioavailable testosterone (BioT) were calculated. Their relationships with NAFLD development or regression were investigated using logistic regression. Results: Baseline concentrations and percentages of cFT and BioT, rather than TT levels, were significantly higher in non-NAFLD postmenopausal women who developed NAFLD after follow-up than in those who did not, while prominently lower in women with NAFLD regression than in those who had sustained NAFLD. Moreover, both higher concentrations and percentages of cFT and BioT were associated with the increased risk of NAFLD development; the fully adjusted ORs (95% CIs) for Q4 Conclusions: Serum concentrations and percentages of cFT and BioT are associated with the progression of NAFLD among postmenopausal women; they could be potential biomarkers for predicting NAFLD progression. Further studies in diverse populations and with a longer follow-up period are needed to verify whether our findings have broader implications.

Indexed as

Non-alcoholic Fatty Liver DiseasePostmenopauseTestosteroneAgedBiomarkersDisease ProgressionFemaleFollow-Up StudiesHumansMiddle AgedProspective StudiesRisk FactorsBiomarkersTestosteroneandrogenbioavailable testosteronecohort study [or longitudinal study]free testosterone (FT)non-alcoholic fatty liver disease (NAFLD)postmenopausal womensex hormone

Identifiers

PMID42137350
PMCPMC13167491

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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.