Evidence map›Paper›PMID 40766861›Full record

ArticleInternational journal of general medicine2025

Serum LCAT as a Gender-Neutral Biomarker for Early Osteoporosis: A Multicenter Cohort Validation Study.

Yali Wen, Shoujun Cheng, Liming Gou, Weihong Zhou, Yishan Li, Ruoxuan Wang, Ji Wu, Xuening Dai, Ming Gao, Lei Wang and 2 more

Abstract read
In one paragraph

Article in International journal of general medicine, 2025. 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

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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. Review
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.

Yali Wen *Department of Orthopedics, Nanjing Drum Tower Hospital, Clinical College of Nanjing University of Chinese Medicine, Nanjing, Jiangsu, People's Republic of China.
Shoujun Cheng *Department of Clinical Laboratory, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, Jiangsu, People's Republic of China.
Liming Gou *Department of Translational Medicine Research Center, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Weihong Zhou *Department of Health Management Centre, Drum Tower Hospital Affiliated to Nanjing University Medical School, Nanjing, Jiangsu, People's Republic of China.
Yishan LiDepartment of Translation Studies, Army Engineering University of PLA, Nanjing, People's Republic of China.
Ruoxuan WangDepartment of Clinical Chinese Medicine, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, People's Republic of China.
Ji WuDepartment of Orthopedics, Sir Run Run Hospital, Nanjing, Jiangsu, People's Republic of China.
Xuening DaiDepartment of Geriatrics, Nanjing Medical University, Nanjing, Jiangsu, People's Republic of China.
Ming GaoDepartment of Endocrinology, Nanjing Medical University, Nanjing, Jiangsu, People's Republic of China.ORCID 0000-0002-1152-5983
Lei WangDepartment of Orthopedics, the First Affiliated Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Bin XueDepartment of Translational Medicine Research Center, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Yinhe WangDepartment of Orthopedics, Nanjing Drum Tower Hospital, Clinical College of Nanjing University of Chinese Medicine, Nanjing, Jiangsu, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: This study aims to identify a novel biomarker for the early detection and prevention of osteoporosis. Methods: A cross-sectional study (n=138, from 497 screened) was conducted at Nanjing Drum Tower Hospital (Sep 2023-Jun 2024). A second multicenter validation cohort (n=165) was collected (Jun 2024-Jan2025) from three hospitals, including 90 controls, 35 osteopenia, and 40 OP cases. Serum LCAT was measured via ELISA. Statistical analyses ( Results: Serum LCAT levels were significantly lower in both the osteopenia (n=32, p<0.01) and osteoporosis groups (n=50, p<0.001) compared with control group (n=56). The results from this second cohort support our previous cross-sectional findings, serum LCAT levels in controls (44.41 ± 14.16), osteopenia (32.15 ± 8.93) and osteoporosis (22.15 ± 7.07). In this multicenter study, serum LCAT levels were evaluated and found to be significantly decreased in the primary osteoporosis group compared to controls across all populations with notable differences by sex (males: U=207.5, p=0.0031; females: U=520.5, p=0.0001) and age (≤55 years: p=0.005; >55 years: p=0.0001). LCAT levels showed positive correlations with T/Z-scores, BMI, ALT, AST, LDL-C, and serum phosphorus, and negative correlations with age and serum creatinine. ROC analysis yielded an AUC of 0.822, with sensitivity and specificity of 75.9% and 78%, respectively. Moreover, serum LCAT levels exhibited significantly higher predictive value for osteoporosis than that of conventional serum 25-hydroxyvitamin D (25OHD) levels. Conclusion: We demonstrate for the first time that reduced serum LCAT concentrations predict osteoporosis risk independently of confounding factors, qualifying it as a promising early-stage diagnostic biomarker. These findings establish LCAT as a demography-invariant diagnostic biomarker for early-stage osteoporosis, suggesting its potential utility in population-wide screening programs.

Indexed as

biomarkerearly detectionhepatogenic factorLCATosteoporosis

Identifiers

PMID40766861
PMCPMC12324063

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