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糖尿病夏科氏足后神经病变进展的长期影响:一项8.5年的前瞻性病例对照研究。

Long-term effects on the progress of neuropathy after diabetic Charcot foot: an 8.5-year prospective case-control study.

作者信息

Jansen Rasmus Bo, Møller Christensen Tomas, Bülow Jens, Rørdam Lene, Holstein Per E, Svendsen Ole Lander

机构信息

Copenhagen Diabetes Foot Center (CODIF), Bispebjerg Hospital, University of Copenhagen, 2400, Copenhagen NV, Denmark.

Department of Endocrinology, Bispebjerg Hospital, University of Copenhagen, 2400, Copenhagen NV, Denmark.

出版信息

BMC Res Notes. 2018 Feb 20;11(1):140. doi: 10.1186/s13104-018-3253-5.

Abstract

OBJECTIVE

Charcot foot is a severe complication to diabetes mellitus, associated with diabetic neuropathy. Any long-term effects of a Charcot foot on the progress of neuropathy are still largely unexplored. The objective was to investigate whether a previous Charcot foot had any long-term effects on the progress of neuropathy.

RESULTS

An 8.5-year follow-up case-control study of 49 individuals with diabetes mellitus, 24 of whom also had Charcot foot at baseline visit in 2005-2007. Neuropathy was assessed with a questionnaire, biothesiometry, heart rate variability and venous occlusion plethysmography. Of the 49 baseline participants, 22 were able to participate in the follow-up. Twelve had passed away in the meantime. Heart rate variability was unchanged in both groups; from 9.7 to 7.2 beats/min (p = 0.053) in the Charcot group, and 14.3 to 12.6 beats/min (p = 0.762) in the control group. Somato-sensoric neuropathy showed no difference between baseline and follow-up in the Charcot group (from 39.1 to 38.5 V) (p = 0.946), but a significantly worsened sensitivity in the control group (from 25.1 to 38.9 V) (p = 0.002). In conclusion, we found that any differences in somatic or cardial autonomic neuropathy present at baseline had disappeared at follow-up after 8.5 years.

摘要

目的

夏科氏足是糖尿病的一种严重并发症,与糖尿病神经病变相关。夏科氏足对神经病变进展的任何长期影响在很大程度上仍未得到充分研究。目的是调查既往夏科氏足是否对神经病变的进展有任何长期影响。

结果

对49名糖尿病患者进行了一项为期8.5年的随访病例对照研究,其中24人在2005 - 2007年基线访视时也患有夏科氏足。通过问卷调查、生物感觉测量、心率变异性和静脉阻塞体积描记法评估神经病变。在49名基线参与者中,22人能够参与随访。在此期间有12人去世。两组的心率变异性均无变化;夏科氏组从9.7次/分钟降至7.2次/分钟(p = 0.053),对照组从14.3次/分钟降至12.6次/分钟(p = 0.762)。体感神经病变在夏科氏组基线和随访之间无差异(从39.1伏降至38.5伏)(p = 0.946),但在对照组中敏感性显著恶化(从25.1伏升至38.9伏)(p = 0.002)。总之,我们发现基线时存在的躯体或心脏自主神经病变的任何差异在8.5年随访后均已消失。

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