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代谢和生活方式因素会加速炎症性非传染性疾病的发病,并改变肠道微生物组。

Metabolic and lifestyle factors accelerate disease onset and alter gut microbiome in inflammatory non-communicable diseases.

机构信息

Institute of Diabetes and Clinical Metabolic Research, University Medical Center Schleswig-Holstein, Düsternbrooker Weg 17, Kiel, 24105, Germany.

Institute for Medical Informatics and Statistics, University Medical Center Schleswig-Holstein, Kiel, Germany.

出版信息

BMC Med. 2024 Oct 24;22(1):493. doi: 10.1186/s12916-024-03709-0.

Abstract

BACKGROUND

Biomedical and lifestyle factors in Western populations have significantly shifted in recent decades, influencing public health and contributing to the increasing prevalence of non-communicable diseases (NCDs) that share inflammation as common pathology.

METHODS

We investigated the relationship between these factors and 11 NCDs in the cross-sectional FoCus cohort (n = 1220), using logistic regression models. Associations with age-at-disease-onset were specifically analyzed for type 2 diabetes (T2D, low-grade chronic inflammation) and inflammatory bowel disease (IBD, high-grade chronic inflammation) in disease-specific cohorts (FoCus-T2D, n = 514; IBD-KC, n = 1110). Important factors for disease risk were identified using Cox-PH-regression models and time-to-event analysis. We further explored the interaction between identified risk factors and gut microbiome composition using linear models.

RESULTS

Lifestyle factors were clearly linked to disease phenotypes, particularly in T2D and IBD. Still, some factors affected only the age-at-onset, but not disease prevalence. High-quality nutrition significantly delayed onset for both IBD and T2D (IBD: HR = 0.81 [0.66; 0.98]; T2D: HR = 0.45 [0.28; 0.72]). Smoking accelerated T2D onset (HR = 1.82 [1.25; 2.65]) but delayed onset in ulcerative colitis (UC: HR = 0.47 [0.28; 0.79]). Higher microbiota diversity delayed IBD onset (Shannon: HR = 0.58 [0.49; 0.71]) but had no effect on T2D. The abundance of specific microbial genera was strongly associated with various biomedical and lifestyle factors in T2D and IBD. In unaffected controls, these effects were smaller or reversed, potentially indicating a greater susceptibility of the gut microbiome to negative influences in T2D and IBD.

CONCLUSIONS

The dual insights into age-at-disease-onset and gut microbiota composition in disease emphasize the role of certain biomedical and lifestyle factors, e.g., nutrition quality, in disease prevention and management. Understanding these relationships provides a foundation for developing targeted strategies to mitigate the impact of metabolic and inflammatory diseases through lifestyle modifications and gut health management.

摘要

背景

近几十年来,西方人群的生物医学和生活方式因素发生了显著变化,这影响了公众健康,并导致了非传染性疾病(NCDs)的患病率不断上升,这些疾病都有炎症这一共同病理。

方法

我们使用逻辑回归模型研究了这些因素与 FoCus 队列中 11 种 NCD 之间的关系(n=1220)。对于特定疾病队列(FoCus-T2D,n=514;IBD-KC,n=1110)中 2 型糖尿病(T2D,低度慢性炎症)和炎症性肠病(IBD,高度慢性炎症),我们特别分析了这些因素与发病年龄之间的关系。使用 Cox-PH 回归模型和时间事件分析确定疾病风险的重要因素。我们还使用线性模型进一步探讨了确定的危险因素与肠道微生物群组成之间的相互作用。

结果

生活方式因素与疾病表型明显相关,尤其是在 T2D 和 IBD 中。尽管如此,一些因素仅影响发病年龄,而不影响疾病的患病率。高质量的营养显著延迟了 IBD 和 T2D 的发病(IBD:HR=0.81[0.66;0.98];T2D:HR=0.45[0.28;0.72])。吸烟加速了 T2D 的发病(HR=1.82[1.25;2.65]),但延缓了溃疡性结肠炎(UC)的发病(HR=0.47[0.28;0.79])。较高的微生物多样性延迟了 IBD 的发病(Shannon:HR=0.58[0.49;0.71]),但对 T2D 没有影响。在未受影响的对照组中,这些影响较小或相反,这可能表明肠道微生物组在 T2D 和 IBD 中更容易受到负面影响。

结论

在疾病中对发病年龄和肠道微生物群组成的双重深入了解,强调了某些生物医学和生活方式因素的作用,例如营养质量,在疾病预防和管理中的作用。了解这些关系为通过生活方式改变和肠道健康管理来制定针对代谢和炎症性疾病的目标策略提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/feee/11515311/e9ca04ca623e/12916_2024_3709_Fig1_HTML.jpg

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