Comprehensive evaluation of diabetes subtypes in a European cohort reveals stronger differences of lifestyle, education and psychosocial parameters compared to metabolic or inflammatory factors.

IF 10.6 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiovascular Diabetology Pub Date : 2025-02-28 DOI:10.1186/s12933-025-02660-5
Nathalie Rohmann, Johannes Epe, Corinna Geisler, Kristina Schlicht, Kathrin Türk, Katharina Hartmann, Lucy Kruse, Julia Koppenhagen, Ahmad Yusuf Kohestani, Tanja Adam, Corinna Bang, Andre Franke, Dominik M Schulte, Tim Hollstein, Matthias Laudes
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Abstract

Background: The traditional binary classification of diabetes into Type 1 and Type 2 fails to capture the heterogeneity among diabetes patients. This study aims to identify and characterize diabetes subtypes within the German FoCus cohort, using the ANDIS cohort's classification framework, and to explore subtype-specific variations in metabolic markers, gut microbiota, lifestyle, social factors, and comorbidities.

Methods: We utilized data from 416 participants (208 with diabetes and 208 matched metabolically healthy controls) from the German FoCus cohort. Participants were classified into five subtypes: severe autoimmune diabetes (SAID)-like, severe insulin-deficient diabetes (SIDD)-like, severe insulin-resistant diabetes (SIRD)-like, mild obesity-related diabetes (MOD)-like, and mild age-related diabetes (MARD)-like. Comprehensive characterization included anthropometric measurements, dietary and physical activity questionnaires, blood biomarker analysis, and gut microbiota profiling.

Results: The subtype distribution in the FoCus cohort accounted to SAID-like: 2.84%, SIDD-like: 30.81%, SIRD-like: 32.23%, MOD-like: 17.54%, MARD-like: 16.59%. Of interest, inflammatory markers (C-reactive protein (CRP) and Interleukin-6 (IL-6)) and glucagon-like peptide-1 (GLP-1) levels were similarly elevated across all subtypes compared to controls, indicating common aspects in Type 2 diabetes molecular pathology despite different clinical phenotypes. While the gut microbiota and dietary patterns only showed minor differences, smoking status, sleep duration, physical activity and psychological aspects varied significantly between the subtypes. In addition, we observed a lower educational status especially for SIDD-like and SIRD-like groups, which should be considered in establishing future diabetes-related patient education programs. In respect to the development of cardio-metabolic comorbidities, we observe not only significant differences in the presence of the diseases but also for their age-of onset, highlighting the need for early preventive intervention strategies.

Conclusions: The study validates the ANDIS classification framework's applicability not only at the time point of manifestation but also in cohorts with pre-existing diabetes. While we did not find major differences regarding the classical metabolic, microbial and nutritional parameters, we identified several significant associations with lifestyle factors. Our findings underscore the importance of personalized, subtype-specific therapies not solely focusing on anthropometric and laboratory markers but comprehensively addressing the patient's own personality and situation of life.

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对欧洲队列中糖尿病亚型的全面评估显示,与代谢或炎症因素相比,生活方式、教育和社会心理参数的差异更大。
背景:将糖尿病分为1型和2型的传统二元分类方法未能反映糖尿病患者的异质性。本研究旨在使用ANDIS队列的分类框架,在德国FoCus队列中识别和表征糖尿病亚型,并探索代谢标志物、肠道微生物群、生活方式、社会因素和合并症的亚型特异性变化。方法:我们利用了来自德国FoCus队列的416名参与者(208名糖尿病患者和208名代谢健康对照者)的数据。参与者被分为五种亚型:严重自身免疫性糖尿病(SAID)样、严重胰岛素缺乏型糖尿病(SIDD)样、严重胰岛素抵抗型糖尿病(SIRD)样、轻度肥胖相关糖尿病(MOD)样和轻度年龄相关糖尿病(MARD)样。综合表征包括人体测量、饮食和身体活动问卷、血液生物标志物分析和肠道微生物群分析。结果:FoCus队列的亚型分布为SAID-like: 2.84%, SIDD-like: 30.81%, srd -like: 32.23%, MOD-like: 17.54%, MARD-like: 16.59%。有趣的是,与对照组相比,所有亚型的炎症标志物(c反应蛋白(CRP)和白细胞介素-6 (IL-6))和胰高血糖素样肽-1 (GLP-1)水平相似地升高,表明尽管临床表型不同,但2型糖尿病分子病理的共同方面。虽然肠道菌群和饮食模式只显示出微小的差异,但吸烟状况、睡眠时间、身体活动和心理方面在不同亚型之间存在显著差异。此外,我们观察到,特别是在sidd样和srd样人群中,教育状况较低,这在建立未来糖尿病相关患者教育计划时应予以考虑。关于心脏代谢合并症的发展,我们不仅观察到疾病存在的显着差异,而且还观察到它们的发病年龄,突出了早期预防干预策略的必要性。结论:该研究验证了ANDIS分类框架不仅在表现时间点上适用性,而且在已有糖尿病的队列中适用性。虽然我们没有发现经典代谢、微生物和营养参数的主要差异,但我们确定了与生活方式因素的几个重要关联。我们的研究结果强调了个性化、亚型特异性治疗的重要性,不仅关注人体测量和实验室标记,而且全面解决患者自身的个性和生活状况。
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来源期刊
Cardiovascular Diabetology
Cardiovascular Diabetology 医学-内分泌学与代谢
CiteScore
12.30
自引率
15.10%
发文量
240
审稿时长
1 months
期刊介绍: Cardiovascular Diabetology is a journal that welcomes manuscripts exploring various aspects of the relationship between diabetes, cardiovascular health, and the metabolic syndrome. We invite submissions related to clinical studies, genetic investigations, experimental research, pharmacological studies, epidemiological analyses, and molecular biology research in this field.
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