非洲 2 型糖尿病和高血压合并症患者的全身炎症加重和动脉粥样硬化。

IF 2.7 Q3 ENDOCRINOLOGY & METABOLISM
Ernst J Groenewald, Bongani B Nkambule, Tawanda M Nyambuya
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引用次数: 0

摘要

目的探讨高血压(HTN)和2型糖尿病(T2D)合并症中常规测量的全身炎症指标及其与动脉粥样硬化的关系:本研究共纳入 70 名 T2D 患者,将其分为两组,即 T2D 和高血压合并症(T2D + HTN)(n = 35/组)。所有测量的实验室参数均采用标准化方法测定:结果:与 T2D 患者相比,T2D + HTN 患者的中性粒细胞/淋巴细胞比值(NLR)升高(P = .0494)。C反应蛋白(CRP)水平也是如此(P = .0298)。值得注意的是,大多数 T2D + HTN 患者[63%(n = 22)]被归类为中度或高度血浆致动脉粥样硬化指数(AIP)。全身炎症的相关性分析显示,CRP 与年龄(r = .24,P = .0477)、CRP 与红细胞计数(r = -.4,P = .0455)、SII 与收缩压(SBP)(r = .33,P = .0056)之间存在显著相关性。但是,炎症特征与脂肪图之间没有关联(P > .05)。我们使用调整了年龄、SBP、CRP 和 SII 的多元回归模型进一步评估了 AIP 升高的预测因素。只有 NLR 是 AIP 的重要预测因子(β = .287,SE:0.1,P = .0046):结论:T2D 合并高血压与炎症和动脉粥样硬化水平加剧有关。NLR 是导致 T2D 患者动脉粥样硬化增加的重要独立风险因素。因此,针对 T2D 和高血压并发症患者使用针对和缓解炎症的治疗策略,对于减少心血管事件 (CVE) 的发生和发展至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aggravated Systemic Inflammation and Atherogenicity in African Patients Living With Type 2 Diabetes and Hypertension Comorbidity.

Objective: To explore routinely measured markers of systemic inflammation in hypertension (HTN) and type 2 diabetes (T2D) comorbidity, and their association with atherogenicity.

Methods: This study included a total of 70 patients with T2D which were categorised into 2 groups, that is with T2D and with HTN comorbidity (T2D + HTN) (n = 35/group). All measured laboratory parameters were determined using standardised methods.

Results: The neutrophil/lymphocyte ratio (NLR) was elevated in patients with T2D + HTN when compared to those with T2D (P = .0494). This was also the case with C-reactive protein (CRP) levels (P < .0001) and systemic immune-inflammation (SII) index (P = .0298). Notably, the majority of patients with T2D + HTN [63% (n = 22)] were classified as having an intermediate or high atherogenic index of plasma (AIP). The correlation analysis of systemic inflammation showed significant associations between CRP and age (r = .24, P = .0477); CRP and red blood cell count (r = -.4, P = .0455), and SII and systolic blood pressure (SBP) (r = .33, P = .0056). However, there was no association between inflammatory profiles and lipograms (P > .05). We further assessed predictors for an elevated AIP using mutivariable regression model adjusted for age, SBP, CRP and SII. Only NLR was a significant predictor of AIP (β = .287, SE: 0.1, P = .0046).

Conclusion: HTN comorbidity in T2D is associated with exacerbated levels of inflammation and atherogenicity. NLR is a significant independent risk factor for increased atherogenicity in patients with T2D. Therefore, the use of therapeutic strategies that target and alleviate inflammation in patients with T2D and HTN comorbidity is imperative in reducing the initiating and progression of cardiovascular events (CVEs).

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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
15
审稿时长
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