1型糖尿病患者小纤维神经病变与晚期糖基化终产物较高的皮肤积聚之间的关系

A. Araszkiewicz, A. Gandecka, M. Nowicki, A. Uruska, A. Malińska, K. Kowalska, B. Wierusz-Wysocka, D. Zozulinska-Ziolkiewicz
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PGP 9.5‑immunoreactive nerve fibers were counted to assess intraepidermal nerve fiber density (IENFD) in skin biopsy. The accumulation of AGEs in the skin was assessed on the basis of skin autofluorescence (AF).  RESULTS Patients with DPN (45%), compared with those without neuropathy, had higher skin AF (2.6 AU [IQR, 2.3-3.1 AU] vs 2.1 AU [IQR, 1.8-2.5 AU]; P <0.001) and lower IENFD (10 fibers/mm [IQR, 7-14 fibers/mm] vs 12 fibers/mm [IQR, 8-16 fibers/mm]; P = 0.005). We found a positive correlation between skin AF and patients' age (Rs = 0.44; P <0.001), diabetes duration (Rs = 0.32; P <0.001), and a negative correlation between skin AF and the estimated glomerular filtration rate (Rs = -0.26, P <0.001) and IENFD (Rs = -0.22; P = 0.004). In a multiple linear regression analysis, skin AF was independently associated with age (β = 0.45; P <0.001), glycated hemoglobin level (β = 0.19; P = 0.007), and IENFD (β = - 0.14; P = 0.04) (R2 = 0.27; P <0.001). In multivariate logistic regression, the presence of DPN was independently associated with skin AF (odds ratio, 4.16; 95% confidence interval, 1.88-9.20; P <0.001). CONCLUSIONS The presence of DPN, and particularly small fiber neuropathy, is associated with a higher accumulation of AGEs in the skin of patients with type 1 diabetes.","PeriodicalId":20343,"journal":{"name":"Polskie Archiwum Medycyny Wewnetrznej","volume":"11 1","pages":"847-853"},"PeriodicalIF":0.0000,"publicationDate":"2016-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"14","resultStr":"{\"title\":\"Association between small fiber neuropathy and higher skin accumulation of advanced glycation end products in patients with type 1 diabetes.\",\"authors\":\"A. Araszkiewicz, A. Gandecka, M. Nowicki, A. Uruska, A. Malińska, K. Kowalska, B. Wierusz-Wysocka, D. 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引用次数: 14

摘要

晚期糖基化终产物(AGEs)在糖尿病周围神经病变(DPN)的发病机制中起着至关重要的作用。该研究的目的是评估长期1型糖尿病患者皮肤中AGEs积累与DPN存在的关系。患者和方法我们评估了178例1型糖尿病患者(99例男性;年龄,43岁[四分位数间距[IQR], 34-54岁];病程25年[IQR, 18-31年])。如果出现以下5种异常中的2种或2种以上,则诊断为DPN:神经病变症状、踝关节反射缺乏、触觉、温度和/或振动感觉受损。计数PGP 9.5免疫反应性神经纤维,以评估皮肤活检中表皮内神经纤维密度(IENFD)。根据皮肤自身荧光(AF)测定AGEs在皮肤中的积累情况。结果:与无神经病变的患者相比,DPN患者(45%)的皮肤AF更高(2.6 AU [IQR, 2.3-3.1 AU] vs 2.1 AU [IQR, 1.8-2.5 AU];P <0.001)和较低的IENFD(10根纤维/mm [IQR, 7-14根纤维/mm] vs 12根纤维/mm [IQR, 8-16根纤维/mm];P = 0.005)。我们发现皮肤房颤与患者年龄呈正相关(Rs = 0.44;P <0.001)、糖尿病病程(Rs = 0.32;P <0.001),皮肤AF与肾小球滤过率(Rs = -0.26, P <0.001)和IENFD (Rs = -0.22;P = 0.004)。在多元线性回归分析中,皮肤AF与年龄独立相关(β = 0.45;P <0.001),糖化血红蛋白水平(β = 0.19;P = 0.007), IENFD (β = - 0.14;P = 0.04) (r2 = 0.27;P < 0.001)。在多因素logistic回归中,DPN的存在与皮肤AF独立相关(优势比4.16;95%置信区间为1.88-9.20;P < 0.001)。结论:DPN的存在,特别是小纤维神经病变,与1型糖尿病患者皮肤中AGEs的较高积累有关。
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Association between small fiber neuropathy and higher skin accumulation of advanced glycation end products in patients with type 1 diabetes.
INTRODUCTION Advanced glycation end products (AGEs) play a crucial role in the pathogenesis of diabetic peripheral neuropathy (DPN). OBJECTIVES The aim of the study was to assess the skin accumulation of AGEs in patients with long‑lasting type 1 diabetes in relation to the presence of DPN. PATIENTS AND METHODS We evaluated 178 patients with type 1 diabetes (99 men; age, 43 years [interquartile range [IQR], 34-54 years]; disease duration, 25 years [IQR, 18-31 years]). DPN was diagnosed if 2 or more of the following 5 abnormalities were present: symptoms of neuropathy, lack of ankle reflexes, and impaired sensation of touch, temperature, and/or vibration. PGP 9.5‑immunoreactive nerve fibers were counted to assess intraepidermal nerve fiber density (IENFD) in skin biopsy. The accumulation of AGEs in the skin was assessed on the basis of skin autofluorescence (AF).  RESULTS Patients with DPN (45%), compared with those without neuropathy, had higher skin AF (2.6 AU [IQR, 2.3-3.1 AU] vs 2.1 AU [IQR, 1.8-2.5 AU]; P <0.001) and lower IENFD (10 fibers/mm [IQR, 7-14 fibers/mm] vs 12 fibers/mm [IQR, 8-16 fibers/mm]; P = 0.005). We found a positive correlation between skin AF and patients' age (Rs = 0.44; P <0.001), diabetes duration (Rs = 0.32; P <0.001), and a negative correlation between skin AF and the estimated glomerular filtration rate (Rs = -0.26, P <0.001) and IENFD (Rs = -0.22; P = 0.004). In a multiple linear regression analysis, skin AF was independently associated with age (β = 0.45; P <0.001), glycated hemoglobin level (β = 0.19; P = 0.007), and IENFD (β = - 0.14; P = 0.04) (R2 = 0.27; P <0.001). In multivariate logistic regression, the presence of DPN was independently associated with skin AF (odds ratio, 4.16; 95% confidence interval, 1.88-9.20; P <0.001). CONCLUSIONS The presence of DPN, and particularly small fiber neuropathy, is associated with a higher accumulation of AGEs in the skin of patients with type 1 diabetes.
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