Faculty of Medicine, Department of Clinical Sciences, Diabetes Research Laboratory, Lund University, Lund, Sweden.
Department of Research and Development, Region Kronoberg, Box 1223, SE-35112, Växjö, Sweden.
Lipids Health Dis. 2020 Oct 14;19(1):223. doi: 10.1186/s12944-020-01397-2.
The receptors for advanced glycation end products (RAGE) are increased in atherosclerotic plaques. Soluble (s)RAGE decreases, whereas the extracellular newly identified receptor for advanced glycation end products (EN-RAGE) increases inflammatory responses mediated by RAGE. The aims were to explore whether sRAGE, EN-RAGE and the EN-RAGE/sRAGE ratio, were associated with the use of lipid-lowering drugs (LLD) and/or antihypertensive drugs (AHD) in patients with type 1 diabetes (T1D).
Cross-sectional design. T1D patients were consecutively recruited from one diabetes clinic. Blood samples were collected, supplemented with data from electronic health records. sRAGE and EN-RAGE were analysed by enzyme linked immunosorbent assays. An EN-RAGE/sRAGE ratio was calculated. Adjustments were performed with inflammatory and metabolic variables, s-creatinine, depression, smoking, physical inactivity, medication, and cardiovascular complications. Multiple regression analyses were performed.
In this study 283 T1D patients (men 56%, 18-59 years) were included. One-hundred and thirty LLD users compared to 153 non-users had lower levels of the EN-RAGE/sRAGE ratio (P = 0.009), and 89 AHD users compared to 194 non-users had lower levels of sRAGE (P = 0.031). The use of LLD (inversely) (B coefficient - 0.158, P = 0.033) and the use of AHD (B coefficient 0.187, P = 0.023) were associated with the EN-RAGE/sRAGE ratio. sRAGE (Lg10) (per unit) (adjusted odds ratio (AOR) = 3.5, 95% CI = 1.4-9.1, P = 0.009), EN-RAGE (Lg10) (per unit) (inversely) (AOR 0.4, 95% CI = 0.2-1.0, P = 0.046), age (P < 0.001), and triglycerides (P < 0.029), were associated with LLD. sRAGE (Lg10) (per unit) (inversely) (AOR = 0.2, 95% CI = 0.1-0.5, P = 0.001), diabetes duration, triglycerides, s-creatinine, and systolic BP (all P values < 0.043), were associated with AHD.
Higher sRAGE levels and lower EN-RAGE levels were linked to the use of LLD, whereas lower sRAGE levels were linked to the use of AHD. No other variables but the use of LLD and the use of AHD were linked to the EN-RAGE/sRAGE ratio. This may be of major importance as sRAGE is an inhibitor and EN-RAGE is a stimulator of inflammatory processes mediated by RAGE.
晚期糖基化终产物(RAGE)的受体在动脉粥样硬化斑块中增加。可溶性(s)RAGE 减少,而新发现的细胞外晚期糖基化终产物受体(EN-RAGE)增加 RAGE 介导的炎症反应。目的是探讨 sRAGE、EN-RAGE 和 EN-RAGE/sRAGE 比值是否与 1 型糖尿病(T1D)患者使用降脂药(LLD)和/或降压药(AHD)有关。
横断面设计。从一家糖尿病诊所连续招募 T1D 患者。采集血样,并从电子健康记录中补充数据。通过酶联免疫吸附试验分析 sRAGE 和 EN-RAGE。计算 EN-RAGE/sRAGE 比值。调整炎症和代谢变量、s-肌酐、抑郁、吸烟、身体活动不足、药物和心血管并发症。进行多元回归分析。
本研究纳入 283 例 T1D 患者(男性 56%,18-59 岁)。与 153 名非使用者相比,130 名 LLD 使用者的 EN-RAGE/sRAGE 比值较低(P=0.009),89 名 AHD 使用者的 sRAGE 水平较低(P=0.031)。LLD 的使用(负相关)(B 系数-0.158,P=0.033)和 AHD 的使用(B 系数 0.187,P=0.023)与 EN-RAGE/sRAGE 比值相关。sRAGE(对数 10)(单位)(调整后优势比(AOR)=3.5,95%CI=1.4-9.1,P=0.009),EN-RAGE(对数 10)(单位)(负相关)(AOR 0.4,95%CI=0.2-1.0,P=0.046),年龄(P<0.001)和甘油三酯(P<0.029),与 LLD 有关。sRAGE(对数 10)(单位)(负相关)(AOR=0.2,95%CI=0.1-0.5,P=0.001)、糖尿病病程、甘油三酯、s-肌酐和收缩压(所有 P 值均<0.043)与 AHD 有关。
较高的 sRAGE 水平和较低的 EN-RAGE 水平与 LLD 的使用有关,而较低的 sRAGE 水平与 AHD 的使用有关。除 LLD 和 AHD 的使用外,没有其他变量与 EN-RAGE/sRAGE 比值有关。这可能非常重要,因为 sRAGE 是 RAGE 介导的炎症过程的抑制剂,而 EN-RAGE 是 RAGE 介导的炎症过程的刺激剂。