Westerbeke Florine H M, Rios-Morales Melany, Attaye Ilias, Nieuwdorp Max
Department of Internal and Experimental Vascular Medicine, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
J Physiol. 2025 Jan 13. doi: 10.1113/JP287316.
Important health disparities are observed in the prevalence of obesity and associated non-communicable diseases (NCDs), including type 2 diabetes (T2D) and metabolic dysfunction-associated steatotic liver disease (MASLD) among ethnic groups. Yet, the underlying factors accounting for these disparities remain poorly understood. Fructose has been widely proposed as a potential mediator of these NCDs, given that hepatic fructose catabolism can result in deleterious metabolic effects, including insulin resistance and hepatic steatosis. Moreover, the fermentation of fructose by the gut microbiota can produce metabolites such as ethanol and acetate, both which serve as potential substrates for de novo lipogenesis (DNL) and could therefore contribute to the development of these metabolic conditions. Significant inter-ethnic differences in gut microbiota composition have been observed. Moreover, fructose consumption varies across ethnic groups, and fructose intake has been demonstrated to significantly alter gut microbiota composition, which can influence its fermenting properties and metabolic effects. Therefore, ethnic differences in gut microbiota composition, which may be influenced by variations in fructose consumption, could contribute to the observed health disparities. This review provides an overview of the complex interactions between host and microbial fructose catabolism, the role of ethnicity in shaping these metabolic processes and their impact on host health. Understanding these interactions could provide insights into the mechanisms driving ethnic health disparities to improve personalized nutrition strategies. KEY POINTS: Dietary fructose consumption has increased substantially over recent decades, which has been associated with the rising prevalence of obesity and non-communicable diseases (NCDs) such as type 2 diabetes and metabolic dysfunction-associated steatotic liver disease. Pronounced disparities among different ethnic groups in NCD prevalence and dietary fructose consumption underscore the need to elucidate the underlying mechanisms of fructose catabolism and its health effects. Together with the well-known toxic effects of hepatic fructose catabolism, emerging evidence highlights a role for the small intestinal microbiota in fermenting sugars like fructose into various bacterial products with potential deleterious metabolic effects. There are significant ethnic differences in gut microbiota composition that, combined with varying fructose consumption, could mediate the observed health disparities. To comprehensively understand the role of the gut microbiota in mediating fructose-induced adverse metabolic effects, future research should focus on the small intestinal microbiota. Future research on fructose - microbiota - host interactions should account for ethnic differences in dietary habits and microbial composition to elucidate the potential role of the gut microbiota in driving the mentioned health disparities.
在不同种族群体中,肥胖及相关非传染性疾病(NCDs)的患病率存在显著的健康差异,这些疾病包括2型糖尿病(T2D)和代谢功能障碍相关脂肪性肝病(MASLD)。然而,导致这些差异的潜在因素仍知之甚少。鉴于肝脏果糖分解代谢会产生有害的代谢影响,包括胰岛素抵抗和肝脂肪变性,果糖已被广泛认为是这些非传染性疾病的潜在介导因素。此外,肠道微生物群对果糖的发酵可产生乙醇和乙酸等代谢产物,这两者都是从头脂肪生成(DNL)的潜在底物,因此可能促成这些代谢状况的发展。已观察到不同种族群体的肠道微生物群组成存在显著差异。此外,不同种族群体的果糖摄入量各不相同,且已证明果糖摄入会显著改变肠道微生物群组成,进而影响其发酵特性和代谢作用。因此,可能受果糖摄入量差异影响的肠道微生物群组成的种族差异,可能是观察到的健康差异的原因。本综述概述了宿主与微生物果糖分解代谢之间的复杂相互作用、种族在塑造这些代谢过程中的作用及其对宿主健康的影响。了解这些相互作用有助于深入了解导致种族健康差异的机制,从而改进个性化营养策略。要点:近几十年来,膳食果糖摄入量大幅增加,这与肥胖及2型糖尿病和代谢功能障碍相关脂肪性肝病等非传染性疾病患病率上升有关。不同种族群体在非传染性疾病患病率和膳食果糖摄入量方面存在明显差异,这凸显了阐明果糖分解代谢及其健康影响的潜在机制的必要性。除了肝脏果糖分解代谢的众所周知的毒性作用外,新出现的证据表明小肠微生物群在将果糖等糖类发酵成具有潜在有害代谢作用的各种细菌产物方面发挥着作用。肠道微生物群组成存在显著的种族差异,这与不同的果糖摄入量共同作用,可能是观察到的健康差异的介导因素。为了全面了解肠道微生物群在介导果糖诱导的不良代谢影响中的作用,未来的研究应聚焦于小肠微生物群。未来关于果糖-微生物群-宿主相互作用的研究应考虑饮食习惯和微生物组成的种族差异,以阐明肠道微生物群在导致上述健康差异中的潜在作用。