In which common chronic conditions can (or cannot) obesity and lifestyle factors explain higher concentrations of C-reactive protein?

IF 5.7 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Diabetes, Obesity & Metabolism Pub Date : 2024-09-20 DOI:10.1111/dom.15949
Jana J. Anderson PhD, Salil V. Deo MD, Paul Welsh PhD, Danny F. MacKay PhD, Frederick K. Ho PhD, Lyn D. Ferguson MD, Carlos Celis-Morales PhD, Jason M. R. Gill PhD, Jill P. Pell MD, Naveed Sattar MD
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Abstract

Aim

Elevated C-reactive protein (CRP), a marker of inflammation, is common in many chronic conditions. We aimed to examine to what extent elevated CRP in chronic conditions could be explained by concurrent adiposity.

Materials and Methods

This cross-sectional study analysed UK Biobank data on 10 chronic conditions reported at baseline. Linear regression models explored the extent to which CRP concentrations were elevated in each condition, unadjusted; adjusted for sociodemographic confounders and lifestyle and body mass index (BMI) in a series of models; or adjusted for BMI and waist circumference together or for adiposity alone.

Results

After exclusion of participants with a potential acute infection at baseline, we tested the association in 292 772 UK Biobank participants. Linear regression showed that elevated CRP concentration was associated with all included conditions. After adjustment for sociodemographic confounders, lifestyle and BMI, chronic kidney disease, heart failure, liver disease, psoriasis, rheumatoid arthritis and chronic obstructive pulmonary disease were still associated with elevated CRP. In contrast, the association between prevalent diabetes, prior myocardial infarction (MI), hypertension and sleep apnoea and CRP could be mostly explained by adiposity alone. For example, the 42% higher CRP concentrations in diabetes compared to those without diabetes in the unadjusted model (lnCRP β: 0.35; 95% confidence interval [CI]: 0.32–0.37, p < 0.001) were completely attenuated after adjustment for BMI (lnCRP β: −0.07; 95% CI: −0.09−0.05, p < 0.001).

Conclusions/Interpretation

In diabetes, MI, hypertension and sleep apnoea and elevated CRP appears to be accounted for by the greater adiposity typically evident in these conditions. However, for the other conditions, systemic inflammation cannot be explained by excess adiposity alone.

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在哪些常见慢性病中,肥胖和生活方式因素可以(或不能)解释较高浓度的 C 反应蛋白?
目的:C反应蛋白(CRP)是炎症的标志物,在许多慢性疾病中都会升高。我们旨在研究慢性病患者的 CRP 升高在多大程度上可以用同时存在的脂肪来解释:这项横断面研究分析了英国生物库中基线报告的 10 种慢性疾病的数据。线性回归模型探讨了每种病症中 CRP 浓度升高的程度,这些模型包括未经调整的模型;在一系列模型中根据社会人口混杂因素、生活方式和体重指数(BMI)进行调整的模型;或根据 BMI 和腰围进行调整的模型,或仅根据肥胖程度进行调整的模型:在排除基线时可能患有急性感染的参与者后,我们对 292 772 名英国生物库参与者进行了相关性测试。线性回归结果表明,CRP 浓度升高与所包含的所有情况都有关联。在对社会人口混杂因素、生活方式和体重指数进行调整后,慢性肾病、心力衰竭、肝病、银屑病、类风湿性关节炎和慢性阻塞性肺病仍与 CRP 升高有关。相比之下,糖尿病、心肌梗死、高血压和睡眠呼吸暂停与 CRP 之间的关系大多可由脂肪含量单独解释。例如,在未经调整的模型中,糖尿病患者的 CRP 浓度比非糖尿病患者高 42% (lnCRP β:0.35; 95% confidence interval [CI]:结论/解释:在糖尿病、心肌梗死、高血压和睡眠呼吸暂停患者中,CRP 的升高似乎是由于这些病症中通常会出现较多的脂肪所致。然而,在其他情况下,全身性炎症不能仅由过多的脂肪来解释。
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来源期刊
Diabetes, Obesity & Metabolism
Diabetes, Obesity & Metabolism 医学-内分泌学与代谢
CiteScore
10.90
自引率
6.90%
发文量
319
审稿时长
3-8 weeks
期刊介绍: Diabetes, Obesity and Metabolism is primarily a journal of clinical and experimental pharmacology and therapeutics covering the interrelated areas of diabetes, obesity and metabolism. The journal prioritises high-quality original research that reports on the effects of new or existing therapies, including dietary, exercise and lifestyle (non-pharmacological) interventions, in any aspect of metabolic and endocrine disease, either in humans or animal and cellular systems. ‘Metabolism’ may relate to lipids, bone and drug metabolism, or broader aspects of endocrine dysfunction. Preclinical pharmacology, pharmacokinetic studies, meta-analyses and those addressing drug safety and tolerability are also highly suitable for publication in this journal. Original research may be published as a main paper or as a research letter.
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