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晚期糖基化终产物低可溶性受体先于类风湿关节炎女性发生心脏代谢事件并可预测该事件。

Low Soluble Receptor for Advanced Glycation End Products Precedes and Predicts Cardiometabolic Events in Women With Rheumatoid Arthritis.

作者信息

Nadali Mitra, Lyngfelt Lovisa, Erlandsson Malin C, Silfverswärd Sofia Töyrä, Andersson Karin M E, Bokarewa Maria I, Pullerits Rille

机构信息

Department of Rheumatology and Inflammation Research, Institution of Medicine, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

Rheumatology Clinic, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

Front Med (Lausanne). 2021 Jan 28;7:594622. doi: 10.3389/fmed.2020.594622. eCollection 2020.

Abstract

Cardiovascular disease (CVD) causes premature mortality in rheumatoid arthritis (RA). Levels of soluble (s)RAGE change with aging, hypertension and hypercholesterolemia. We assessed whether sRAGE was associated with increased risk of CVD in RA patients. Serum sRAGE was measured in 184 female RA patients and analyzed with respect to CVD risk estimated by the Framingham algorithm (eCVR), metabolic profile and inflammation. Levels of sRAGE in 13 patients with known cardio-metabolic morbidity defined the cut-off for low sRAGE. Prospective 5-year follow-up of new CV and metabolic events was completed. Low sRAGE was significantly associated with previous history and with new imminent cardiometabolic events in the prospective follow-up of RA patients. In both cases, low sRAGE reflected higher estimation of CVR in those patients. Low sRAGE was attributed to adverse metabolic parameters including high fasting plasma glucose and body fat content rather than inflammation. The association of sRAGE and poor metabolic profile was prominent in patients younger than 50 years. This study points at low sRAGE as a marker of metabolic failure developed during chronic inflammation. It highlights the importance for monitoring metabolic health in female RA patients for timely prevention of CVD. ClinicalTrials.gov with ID NCT03449589. Registered 28, February 2018.

摘要

心血管疾病(CVD)可导致类风湿关节炎(RA)患者过早死亡。可溶性(s)RAGE水平会随衰老、高血压和高胆固醇血症而变化。我们评估了sRAGE是否与RA患者发生CVD的风险增加相关。对184例女性RA患者的血清sRAGE进行了检测,并根据弗雷明汉算法(eCVR)估计的CVD风险、代谢状况和炎症情况进行了分析。13例已知存在心脏代谢疾病的患者的sRAGE水平确定了低sRAGE的临界值。完成了对新的心血管和代谢事件的前瞻性5年随访。在RA患者的前瞻性随访中,低sRAGE与既往病史以及新的即将发生的心脏代谢事件显著相关。在这两种情况下,低sRAGE都反映出这些患者的CVR估计值较高。低sRAGE归因于不良代谢参数,包括高空腹血糖和体脂含量,而非炎症。sRAGE与不良代谢状况的关联在50岁以下患者中尤为突出。本研究指出低sRAGE是慢性炎症期间发生的代谢功能衰竭的一个标志物。它强调了监测女性RA患者代谢健康对于及时预防CVD的重要性。ClinicalTrials.gov标识符为NCT03449589。于2018年2月28日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b223/7876441/0b2dbb1caaf4/fmed-07-594622-g0001.jpg

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