Female sex is a risk factor for painful diabetic peripheral neuropathy: the EURODIAB prospective diabetes complications study

被引:25
作者
Elliott, Jackie [1 ,2 ]
Sloan, Gordon [1 ,2 ]
Stevens, Lynda [3 ]
Selvarajah, Dinesh [1 ,2 ]
Cruccu, Giorgio [4 ]
Gandhi, Rajiv A. [1 ,2 ]
Kempler, Peter [5 ]
Fuller, John H. [6 ]
Chaturvedi, Nishi [7 ]
Tesfaye, Solomon [1 ,2 ]
机构
[1] Royal Hallamshire Hosp, Diabet Res Unit, Sheffield, S Yorkshire, England
[2] Univ Sheffield, Dept Oncol & Metab, Sheffield, S Yorkshire, England
[3] UCL, Dept Epidemiol & Publ Hlth, London, England
[4] Univ Roma La Sapienza, Dept Neurol Sci, Rome, Italy
[5] Semmelweis Univ, Dept Med 1, Budapest, Hungary
[6] Imperial Coll Sci Technol & Med, Epidemiol & Publ Hlth, London, England
[7] UCL, MRC Unit Lifelong Hlth & Ageing, Inst Cardiovasc Sci, London, England
基金
英国惠康基金;
关键词
Diabetic peripheral neuropathy; Epidemiology; Neuropathic pain; Painful diabetic neuropathy; Painful neuropathy; Type 1 diabetes mellitus; PREVALENCE; POLYNEUROPATHY; PHENOTYPE; SEVERITY;
D O I
10.1007/s00125-023-06025-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesisWhile the risk factors for diabetic peripheral neuropathy (DPN) are now well recognised, the risk factors for painful DPN remain unknown. We performed analysis of the EURODIAB Prospective Complications Study data to elucidate the incidence and risk factors of painful DPN.MethodsThe EURODIAB Prospective Complications Study recruited 3250 participants with type 1 diabetes who were followed up for 7.3 +/- 0.6 (mean +/- SD) years. To evaluate DPN, a standardised protocol was used, including clinical assessment, quantitative sensory testing and autonomic function tests. Painful DPN (defined as painful neuropathic symptoms in the legs in participants with confirmed DPN) was assessed at baseline and follow-up.ResultsAt baseline, 234 (25.2%) out of 927 participants with DPN had painful DPN. At follow-up, incident DPN developed in 276 (23.5%) of 1172 participants. Of these, 41 (14.9%) had incident painful DPN. Most of the participants who developed incident painful DPN were female (73% vs 48% painless DPN p=0.003) and this remained significant after adjustment for duration of diabetes and HbA1c (OR 2.69 [95% CI 1.41, 6.23], p=0.004). The proportion of participants with macro- or microalbuminuria was lower in those with painful DPN compared with painless DPN (15% vs 34%, p=0.02), and this association remained after adjusting for HbA1c, diabetes duration and sex (p=0.03).Conclusions/interpretationIn this first prospective study to investigate the risk factors for painful DPN, we definitively demonstrate that female sex is a risk factor for painful DPN. Additionally, there is less evidence of diabetic nephropathy in incident painful, compared with painless, DPN. Thus, painful DPN is not driven by cardiometabolic factors traditionally associated with microvascular disease. Sex differences may therefore play an important role in the pathophysiology of neuropathic pain in diabetes. Future studies need to look at psychosocial, genetic and other factors in the development of painful DPN.
引用
收藏
页码:190 / 198
页数:9
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