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Article

Novel Targets for Precision Nutrition: Insulin Resistance and Phenotypic Age Mediate the Protective Effect of Gut Microbiota-Targeted Diet on Metabolic Syndrome

1
Faculty of Humanities and Social Sciences, Macau Polytechnic University, Macau 999078, China
2
Vocational and Technical College, Shanghai Jian Qiao University, Shanghai 201315, China
3
School of Life Sciences, Shanghai Normal University, Shanghai 200234, China
4
Faculty of Applied Sciences, Macao Polytechnic University, Macao 999078, China
5
Higher Education Institute, East China Normal University, Shanghai 200062, China
6
Department of Physical Education, Shanghai Maritime University, Shanghai 201306, China
*
Authors to whom correspondence should be addressed.
Obesities 2026, 6(3), 33; https://doi.org/10.3390/obesities6030033
Submission received: 6 April 2026 / Revised: 25 May 2026 / Accepted: 26 May 2026 / Published: 28 May 2026

Abstract

Background: The dietary index for gut microbiota (DI-GM) holds promise for improving metabolic status, yet its mechanistic insight into metabolic syndrome (MetS) is unclear. Methods: In this cross-sectional study, we analyzed data from 20,800 participants in the NHANES (2005–2018). The DI-GM was developed based on dietary patterns, and MetS was defined according to the NCEP-ATP III criteria. Global DI-GM scores came from the Global Dietary Database (164 nations), with MetS burden estimation employing Global Burden of Disease data. We explored mediation by phenotypic age, insulin resistance (HOMA-IR), and inflammation. Secondary analyses involved subgroup stratification, restricted cubic splines (RCS), sensitivity testing, propensity score matching, and multiple imputations. Results: Globally, higher national DI-GM correlated inversely with metabolic risk factor frequency and major MetS sequelae. NHANES analysis found each one-unit DI-GM rise was associated with an 11% lower MetS likelihood (adjusted OR = 0.89, 95%CI: 0.87–0.91). RCS indicated a non-linear exposure–response curve, with prevalence reduction stabilizing above DI-GM = 4.972. Stratification showed significant effect modification by race/ethnicity, education, and income (p-interaction < 0.05). Mediation analysis identified significant roles for phenotypic aging (24.77%) and HOMA-IR (47.98%), but not inflammation (0.54%). Conclusions: A DI-GM-aligned diet correlated with lower MetS prevalence, with insulin sensitivity and phenotypic aging accounting for part of this association. Microbiota-targeted nutrition guidelines for MetS should prioritize metabolic health over anti-inflammation.
Keywords: impaired insulin sensitivity; biological age; mediation effects; socioeconomic strata; precision nutrition; public health impaired insulin sensitivity; biological age; mediation effects; socioeconomic strata; precision nutrition; public health

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MDPI and ACS Style

Li, X.; Guan, J.; Liu, Y.; Luo, S.; Gong, Y.; Jiang, H.; Shao, C. Novel Targets for Precision Nutrition: Insulin Resistance and Phenotypic Age Mediate the Protective Effect of Gut Microbiota-Targeted Diet on Metabolic Syndrome. Obesities 2026, 6, 33. https://doi.org/10.3390/obesities6030033

AMA Style

Li X, Guan J, Liu Y, Luo S, Gong Y, Jiang H, Shao C. Novel Targets for Precision Nutrition: Insulin Resistance and Phenotypic Age Mediate the Protective Effect of Gut Microbiota-Targeted Diet on Metabolic Syndrome. Obesities. 2026; 6(3):33. https://doi.org/10.3390/obesities6030033

Chicago/Turabian Style

Li, Xiaodan, Jialu Guan, Ying Liu, Shengcong Luo, Youwu Gong, Hongke Jiang, and Changzhuan Shao. 2026. "Novel Targets for Precision Nutrition: Insulin Resistance and Phenotypic Age Mediate the Protective Effect of Gut Microbiota-Targeted Diet on Metabolic Syndrome" Obesities 6, no. 3: 33. https://doi.org/10.3390/obesities6030033

APA Style

Li, X., Guan, J., Liu, Y., Luo, S., Gong, Y., Jiang, H., & Shao, C. (2026). Novel Targets for Precision Nutrition: Insulin Resistance and Phenotypic Age Mediate the Protective Effect of Gut Microbiota-Targeted Diet on Metabolic Syndrome. Obesities, 6(3), 33. https://doi.org/10.3390/obesities6030033

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