Evidence map›Paper›PMID 40524225›Full record

ArticleDiabetology & metabolic syndrome2025

The role of plasma glucose in association of food-specific serum immunoglobulin G reactivity with metabolic dysfunction-associated fatty liver disease: a real-world cross-sectional study.

Guanchao Sun, Wenjuan Wu, Binbin Su, Ru Zhang, Xiaoyu Dong, Lihui Wang, Shiping Xu, Hui Shi

Abstract read
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Article in Diabetology & metabolic syndrome, 2025. 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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5 · Who and what money

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8 authors.

Guanchao Sun *Department of Gastroenterology, Second Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Wenjuan Wu *Department of Gastroenterology, Second Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Binbin Su *Department of Gastroenterology, Second Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Ru ZhangDepartment of Gastroenterology, Second Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Xiaoyu DongDepartment of Gastroenterology, Second Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Lihui WangDepartment of Gastroenterology, Second Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Shiping XuDepartment of Gastroenterology, Second Medical Center of Chinese PLA General Hospital, Beijing, 100853, China. xushiping@301hospital.com.cn.
Hui ShiDepartment of Gastroenterology, Second Medical Center of Chinese PLA General Hospital, Beijing, 100853, China. shihui3012187@163.com.

Funding

National Key Research and Development Program of China: Screening of Aging-Related Core Factors and Development of Targeted Drugs 2024YFA1109103
6 · The paper itself

Abstract

backgroundAs the immune response product to food antigens, food-specific serum immunoglobulin G reactivity (FSsIgGR) has been reported the clinical relevance to metabolic disorders, but its connections to metabolic dysfunction-associated fatty liver disease (MAFLD) remain underexplored, particularly within Chinese populations. Understanding this association could facilitate personal diet modification for MAFLD treatment. We investigated the association between FSsIgGR and MAFLD and the mediating roles of plasma glucose markers, specifically fasting blood glucose (FPG) and hemoglobin A1c (HbA1c).

methodsThis study utilized data from the Second Medical Center of the Chinese PLA General Hospital from 2017 to 2021, to analyze the relationships between FSsIgGR and MAFLD in 25,928 participants. Using a robust sampling method and adjusting for various covariates, we explored both linear and nonlinear associations using linear regression models, restricted cubic splines (RCS), subgroup analysis, and sensitivity analysis. Furthermore, mediation analyses were conducted to evaluate the role of plasma glucose markers, such as FPG and HbA1c, in these relationships.

resultsThe overall prevalence of FSsIgGR-positive and MAFLD was 60.8% and 53.5%, respectively, with a mean age of 49.6 ± 9.7 years (68.8% male). Both the quantity and level of FSsIgGR exhibited negatively linear associations with MAFLD (OR 0.98, 95% CI 0.96-0.99, P = 0.041; OR 0.99, 95% CI 0.97-0.99, P = 0.044), even after adjusting for multiple covariates. Sensitivity analyses supported the robustness of these findings. Of note, subgroup analysis showed that FSsIgGR still was negatively associated with MAFLD patients without Type 2 diabetes (OR 0.98, 95% CI 0.95-0.99) or insulin resistance (OR 0.97, 95% CI 0.94-0.99), while that statistical significance of associations disappears in MAFLD patients with Type 2 diabetes or insulin resistance. Furthermore, plasma glucose markers, particularly FPG, significantly mediated the relationship between FSsIgGR and MAFLD, with indirect effects estimated at 15.5% (P = 0.0002).

conclusionsThese findings indicated FSsIgGR was linked to a reduced risk of MAFLD, particularly MAFLD without Type 2 diabetes or insulin resistance, and plasma glucose mediated that process. Further research is needed to elucidate the mechanism underlying that association, expecting to provide reference for personalized diet of MAFLD patients.

Indexed as

Cross-sectional studyFood-specific serum immunoglobulin G reactivityMediation analysesMetabolic dysfunction-associated fatty liver diseasePlasma glucose

Identifiers

PMID40524225
PMCPMC12168319

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