Evidence map›Paper›PMID 42487130›Full record

ReviewChinese medicine2026

Medicine-food homologous bioactives in metabolic dysregulation-associated osteoporosis: a review of preclinical evidence and potential liver-bone and gut-bone actions.

Wen Fan, Beilei Shi, Ze Gao, Yan Cui, Xiaofeng Zhu

Abstract readReview
In one paragraph

Review in Chinese medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Wen Fan *School of Traditional Chinese Medicine, Jinan University, Guangzhou, 510630, Guangdong, People's Republic of China.ORCID https://orcid.org/0009-0009-7084-4819
Beilei Shi *School of Traditional Chinese Medicine, Jinan University, Guangzhou, 510630, Guangdong, People's Republic of China.
Ze Gao *The First Affiliated Hospital of Jinan University, Guangzhou, 510630, Guangdong, People's Republic of China.
Yan CuiThe First Affiliated Hospital of Jinan University, Guangzhou, 510630, Guangdong, People's Republic of China. cuiyan@jnu.edu.cn.
Xiaofeng ZhuSchool of Traditional Chinese Medicine, Jinan University, Guangzhou, 510630, Guangdong, People's Republic of China. zxiaof@jnu.edu.cn.

Funding

he Key Laboratory of Traditional Chinese Medicine Informatization of Guangdong Province 2021B1212040007the Integrated Project of the Joint Fund for Regional Innovation and Development of the National Natural Science Foundation of China U24A6013the Key Project of the Major Science and Technology Project of Traditional Chinese Medicine in Guangzhou Area by the Guangzhou Health Commission 2025ZD005the Key R & D Program Project of the Guangzhou Science and Technology Bureau 2024B03J1287the National Natural Science Foundation of China 82274376
6 · The paper itself

Abstract

backgroundOsteoporosis is increasingly linked to metabolic dysregulation. Medicine-food homologous (MFH) materials contain diverse natural bioactives with reported osteoprotective effects, but their overall evidence landscape remains insufficiently integrated. PURPOSE: To synthesize preclinical evidence on MFH-derived bioactives that improve osteoporosis-related phenotypes and to discuss their possible trans-organ actions under metabolic disturbance.

methodsPubMed, Web of Science, Scopus, and CNKI were searched from January 2000 to September 2025. Original in vivo or in vitro studies were included when a defined MFH-derived constituent or standardized single-material extract was tested in an osteoporosis-relevant model and reported both bone-related and metabolism-related outcomes.

resultsA total of 38 bioactive components from 24 MFH materials were identified and regrouped into seven higher-level natural-product categories, including flavonoids, phenolic and polyphenolic compounds, polysaccharides, saponins, terpenoids, proteins/peptides, and other specialized metabolites. Across studies, osteoprotective effects were frequently accompanied by parallel improvements in lipid metabolism, inflammatory status, oxidative stress, gut microbiota, or related metabolites. These findings suggest that MFH bioactives may act beyond bone-local signaling alone. In the discussion, this pattern was further interpreted through liver-bone and gut-bone.

conclusionMFH-derived bioactives show potential to improve osteoporosis-related phenotypes and may exert broader systemic regulatory effects, although specific mediators and causal links still require validation.

Indexed as

Gut-bone axisIndirect pharmacologyLiver-bone axisMFH bioactivesOsteoporosis

Identifiers

PMID42487130
PMCPMC13390145

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.