Diabetic polyneuropathies: update on research definition, diagnostic criteria and estimation of severity

被引:340
作者
Dyck, Peter J. [1 ]
Albers, James W. [2 ]
Andersen, Henning [3 ]
Arezzo, Joseph C. [4 ]
Biessels, Geert-Jan [5 ]
Bril, Vera [6 ]
Feldman, Eva L. [2 ]
Litchy, William J. [1 ]
O'Brien, Peter C. [7 ]
Russell, James W. [8 ]
机构
[1] Mayo Clin, Dept Neurol, Rochester, MN 55905 USA
[2] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
[3] Aarhus Univ Hosp, DK-8000 Aarhus, Denmark
[4] Albert Einstein Coll Med, Dept Neurosci, New York, NY USA
[5] Rudolf Magnus Inst Pharmacol, Utrecht, Netherlands
[6] Univ Toronto, Dept Med, Toronto, ON, Canada
[7] Mayo Clin, Div Biostat, Rochester, MN 55905 USA
[8] Univ Maryland, Dept Neurol, Baltimore, MD 21201 USA
关键词
diabetic polyneuropathy; diabetic sensorimotor polyneuropathy; atypical diabetic polyneuropathy; classification; definitions; IMPAIRED GLUCOSE-TOLERANCE; NERVE-CONDUCTION; MICROVASCULAR COMPLICATIONS; ENDONEURIAL MICROVESSELS; PERIPHERAL NEUROPATHY; NATURAL-HISTORY; RISK-FACTORS; DESIGN; REPRODUCIBILITY; ABNORMALITIES;
D O I
10.1002/dmrr.1226
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Prior to a joint meeting of the Neurodiab Association and International Symposium on Diabetic Neuropathy held in Toronto, Ontario, Canada, 13-18 October 2009, Solomon Tesfaye, Sheffield, UK, convened a panel of neuromuscular experts to provide an update on polyneuropathies associated with diabetes (Toronto Consensus Panels on DPNs, 2009). Herein, we provide definitions of typical and atypical diabetic polyneuropathies (DPNs), diagnostic criteria, and approaches to diagnose sensorimotor polyneuropathy as well as to estimate severity. Diabetic sensorimotor polyneuropathy (DSPN), or typical DPN, usually develops on long-standing hyperglycaemia, consequent metabolic derangements and microvessel alterations. It is frequently associated with microvessel retinal and kidney disease - but other causes must be excluded. By contrast, atypical DPNs are intercurrent painful and autonomic small-fibre polyneuropathies. Recognizing that there is a need to detect and estimate severity of DSPN validly and reproducibly, we define subclinical DSPN using nerve conduction criteria and define possible, probable, and confirmed clinical levels of DSPN. For conduct of epidemiologic surveys and randomized controlled trials, it is necessary to pre-specify which attributes of nerve conduction are to be used, the criterion for diagnosis, reference values, correction for applicable variables, and the specific criterion for DSPN. Herein, we provide the performance characteristics of several criteria for the diagnosis of sensorimotor polyneuropathy in healthy subject-and diabetic subject cohorts. Also outlined here are staged and continuous approaches to estimate severity of DSPN. Copyright (C) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:620 / 628
页数:9
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