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尿肝型脂肪酸结合蛋白可预测 1 型糖尿病患者的肾病进展。

Urinary liver-type fatty acid-binding protein predicts progression to nephropathy in type 1 diabetic patients.

机构信息

Steno Diabetes Center, Gentofte, Denmark.

出版信息

Diabetes Care. 2010 Jun;33(6):1320-4. doi: 10.2337/dc09-2242. Epub 2010 Feb 25.

Abstract

OBJECTIVE

Urinary liver-type fatty acid-binding protein (u-LFABP) is a marker of tubulointerstitial inflammation and has been shown to be increased in patients with type 1 diabetes and is further increased in patients who progress to micro- and macroalbuminuria. Our aim was to evaluate u-LFABP as a predictor of progression to micro- and macroalbuminuria in type 1 diabetes.

RESEARCH DESIGN AND METHODS

From an inception cohort of 277 patients, u-LFABP, adjusted for urinary creatinine (enzyme-linked immunosorbent assay), was measured in 24-h urine samples from 165 normoalbuminuric patients 9.6 +/- 3.5 (mean +/-SD) years after onset of type 1 diabetes. The outcome measured was development of persistent micro- or macroalbuminuria or death.

RESULTS

Patients were followed for a median of 18 (range 1-19) years; 39 progressed to microalbuminuria, 8 of those progressed further to macroalbuminuria, and 24 died. In a Cox regression model, baseline log u-LFABP levels predicted the development of microalbuminuria, adjusted for known risk factors (sex, age, A1C, systolic and diastolic blood pressure, albumin excretion rate, serum creatinine, and smoking) (hazard ratio [HR] 2.3 [95% CI 1.1-4.6]) and log u-LFABP predicted mortality (adjusted HR 3.0 [1.3-7.0]). u-LFABP (above versus below the median) predicted the development of macroalbuminuria (adjusted HR 2.6 [1.2-5.4]). As a continuous variable, u-LFABP tended to predict macroalbuminuria (HR 1.9, P = 0.2), but numbers were small.

CONCLUSIONS

High levels of the tubular inflammation marker u-LFABP predict the initiation and progression to diabetic nephropathy and all-cause mortality, independent of urinary albumin excretion rate and other established risk factors.

摘要

目的

尿肝型脂肪酸结合蛋白(u-LFABP)是肾小管间质炎症的标志物,已在 1 型糖尿病患者中显示增加,并在进展为微量白蛋白尿和大量白蛋白尿的患者中进一步增加。我们的目的是评估 u-LFABP 作为 1 型糖尿病进展为微量白蛋白尿和大量白蛋白尿的预测指标。

研究设计和方法

从一个 277 例患者的起始队列中,在 1 型糖尿病发病后 9.6 +/- 3.5(平均值 +/-SD)年,对 165 例正常白蛋白尿患者的 24 小时尿液样本中进行 u-LFABP(酶联免疫吸附测定法)校正的 u-LFABP 测量。测量的结果是持续微量白蛋白尿或大量白蛋白尿或死亡的发展。

结果

患者平均随访中位数为 18 年(范围 1-19 年);39 例进展为微量白蛋白尿,其中 8 例进一步进展为大量白蛋白尿,24 例死亡。在 Cox 回归模型中,基线对数 u-LFABP 水平预测了微量白蛋白尿的发生,校正了已知的危险因素(性别、年龄、A1C、收缩压和舒张压、白蛋白排泄率、血清肌酐和吸烟)(危险比 [HR] 2.3 [95% CI 1.1-4.6]),并且 u-LFABP 预测了死亡率(调整后的 HR 3.0 [1.3-7.0])。u-LFABP(高于或低于中位数)预测了大量白蛋白尿的发生(调整后的 HR 2.6 [1.2-5.4])。作为连续变量,u-LFABP 倾向于预测大量白蛋白尿(HR 1.9,P = 0.2),但数量较小。

结论

肾小管炎症标志物 u-LFABP 的高水平预测了糖尿病肾病和全因死亡率的发生和进展,独立于尿白蛋白排泄率和其他已建立的危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c451/2875447/97a070a04b05/zdc0051082450001.jpg

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