Women4Health 队列:研究女性特有的心血管代谢调节机制的独特队列。

European heart journal open Pub Date : 2024-02-27 eCollection Date: 2024-03-01 DOI:10.1093/ehjopen/oeae012
Fabio Busonero, Stefania Lenarduzzi, Francesca Crobu, Roberta Marie Gentile, Andrea Carta, Francesco Cracco, Andrea Maschio, Silvia Camarda, Michele Marongiu, Daniela Zanetti, Claudio Conversano, Giovanni Di Lorenzo, Daniela Mazzà, Francesco De Seta, Giorgia Girotto, Serena Sanna
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引用次数: 0

摘要

目的:流行病学研究表明,不同性别在心血管和新陈代谢疾病的临床表现、严重程度和病情发展方面存在相关差异。迄今为止,这些差异背后的机制仍不为人知。鉴于此类疾病的发病率不断上升,针对不同性别的既有和新出现的风险因素(如血糖和/或血脂代谢障碍、性激素和肠道微生物组)进行研究至关重要。即使在平衡状态下,性激素、肠道微生物组和宿主血糖和/或脂质代谢之间的关系在很大程度上也是未知的。然而,这一知识空白对于确定在疾病情况下可能被破坏的关键机制至关重要:在此,我们将介绍 "Women4Health(W4H)"队列,这是一个独特的队列,由多达 300 名健康女性组成,她们在自然月经周期中接受随访,建立该队列的主要目的是利用多组学策略研究性激素和肠道微生物群变化在调节体内脂质和葡萄糖代谢过程中的综合作用。此外,W4H 队列还将考虑到女性特有的另一个生态系统--阴道微生物群,研究其与肠道微生物群的相互作用,并首次探索其在心脏代谢紊乱中的作用:W4H队列研究为提高目前对女性特有的心脏代谢调节机制的认识奠定了基础。结论:W4H 队列研究为提高当前对女性特有的心脏代谢调节机制的认识奠定了基础,有望将对宿主-微生物群相互作用的认识转化为预防和治疗方法,从而实现个性化保健。
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The Women4Health cohort: a unique cohort to study women-specific mechanisms of cardio-metabolic regulation.

Aims: Epidemiological research has shown relevant differences between sexes in clinical manifestations, severity, and progression of cardiovascular and metabolic disorders. To date, the mechanisms underlying these differences remain unknown. Given the rising incidence of such diseases, gender-specific research on established and emerging risk factors, such as dysfunction of glycaemic and/or lipid metabolism, of sex hormones and of gut microbiome, is of paramount importance. The relationships between sex hormones, gut microbiome, and host glycaemic and/or lipid metabolism are largely unknown even in the homoeostasis status. Yet this knowledge gap would be pivotal to pinpoint to key mechanisms that are likely to be disrupted in disease context.

Methods and results: Here we present the Women4Health (W4H) cohort, a unique cohort comprising up to 300 healthy women followed up during a natural menstrual cycle, set up with the primary goal to investigate the combined role of sex hormones and gut microbiota variations in regulating host lipid and glucose metabolism during homoeostasis, using a multi-omics strategy. Additionally, the W4H cohort will take into consideration another ecosystem that is unique to women, the vaginal microbiome, investigating its interaction with gut microbiome and exploring-for the first time-its role in cardiometabolic disorders.

Conclusion: The W4H cohort study lays a foundation for improving current knowledge of women-specific mechanisms in cardiometabolic regulation. It aspires to transform insights on host-microbiota interactions into prevention and therapeutic approaches for personalized health care.

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