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首页> 外文期刊>Diabetes care >Does the prevailing hypothesis that small-fiber dysfunction precedes large-fiber dysfunction apply to type 1 diabetic patients?
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Does the prevailing hypothesis that small-fiber dysfunction precedes large-fiber dysfunction apply to type 1 diabetic patients?

机译:小纤维功能障碍先于大纤维功能障碍的普遍假设是否适用于1型糖尿病患者?

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OBJECTIVE: The prevailing hypothesis that early subclinical small-fiber injury precedes large-fiber damage in diabetic sensorimotor polyneuropathy (DSP) is based on lower intraepithelial nerve fiber density in type 2 prediabetic patients despite normal nerve conduction studies (NCSs). We aimed to confirm the same hypothesis in type 1 diabetic patients by examining whether: 1) subjects without DSP include a spectrum with both normal and abnormal small-fiber measures and 2) subjects with DSP have concurrent evidence of abnormal small-fiber measures. RESEARCH DESIGN AND METHODS: A healthy control population (n = 53) was used to generate threshold values for four small-fiber tests: cooling detection thresholds (CDTs), laser Doppler imaging of heat-evoked flare (LDIflare), heart rate variability (HRV), and corneal confocal microscopy. Based on NCS results, type 1 diabetic patients (n = 131) were dichotomized according to the presence or absence of DSP. RESULTS: Threshold values derived from healthy control subjects were 26.5°C, 1.4 cm 2, 13%, and 12.9 mm/mm2 for CDT, LDIflare, HRV, and corneal nerve fiber length, respectively. Among type 1 diabetic patients, 57 of 131 had evidence of DSP, and 74 of 133 did not. Using abnormality of any small-fiber test to define small-fiber dysfunction, 55 of 57 (96.5%) DSP patients and 39 of 74 (52.7%) control subjects without DSP had concurrent small-fiber damage. The severity of small-fiber abnormalities worsened with an increasing number of NCS abnormalities (ANOVA, P < 0.01). CONCLUSIONS: Our findings in type 1 diabetes support the prevailing hypothesis that small-fiber dysfunction occurs early in DSP. However, further research is required to determine which combination of small-fiber tests is most suitable as a surrogate marker in clinical trials.
机译:目的:流行的假说是,糖尿病性感觉运动性多发性神经病(DSP)的早期亚临床小纤维损伤先于大纤维损伤是基于尽管神经传导研究(NCS)正常的2型糖尿病前期患者的上皮内神经纤维密度较低。我们旨在通过检查以下方面来证实1型糖尿病患者的相同假设:1)没有DSP的受试者包括正常和异常的小纤维措施的频谱,以及2)患有DSP的受试者同时出现异常的小纤维措施的证据。研究设计与方法:健康对照组(n = 53)用于生成四个小纤维测试的阈值:冷却检测阈值(CDT),热诱发耀斑的激光多普勒成像(LDIflare),心率变异性( HRV)和角膜共聚焦显微镜检查。根据NCS结果,根据是否存在DSP将1型糖尿病患者(n = 131)二分。结果:健康对照组的CDT,LDIflare,HRV和角膜神经纤维长度的阈值分别为26.5°C,1.4 cm 2、13%和12.9 mm / mm2。在1型糖尿病患者中,131名中的57名有DSP证据,而133名中的74名没有DSP证据。使用任何小纤维测试的异常来定义小纤维功能障碍,没有DSP的57名(55.6%)DSP患者中有55名(74.5%)有74名(52.7%)对照组没有同时发生小纤维损伤。随着NCS异常数量的增加,小纤维异常的严重性恶化(ANOVA,P <0.01)。结论:我们在1型糖尿病中的发现支持了普遍的假设,即DSP早期会出现小纤维功能障碍。但是,需要进一步的研究来确定哪种小纤维测试组合最适合作为临床试验中的替代指标。

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