A Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic Pain

被引:59
作者
Meng, Weihua [1 ]
Deshmukh, Harshal A. [1 ]
Donnelly, Louise A. [2 ]
Torrance, Nicola [1 ]
Colhoun, Helen M. [1 ]
Palmer, Colin N. A. [2 ]
Smith, Blair H. [1 ]
机构
[1] Univ Dundee, Ninewells Hosp & Med Sch, Med Res Inst, Div Populat Hlth Sci, Dundee DD2 4BF, Scotland
[2] Univ Dundee, Ninewells Hosp & Med Sch, Med Res Inst, Ctr Pharmacogenet & Pharmacogenom, Dundee DD1 9SY, Scotland
基金
英国惠康基金;
关键词
Neuropathic pain; GWAS; Heritability; Sex-specific; TOLL-LIKE RECEPTORS; GENERAL-POPULATION; NERVE INJURY; PHARMACOLOGICAL-TREATMENT; RISK-FACTORS; EPIDEMIOLOGY; SENSITIVITY; ACTIVATION; MODEL; MICE;
D O I
10.1016/j.ebiom.2015.08.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Neuropathic pain is defined as pain arising as a direct consequence of a lesion or a disease affecting the somatosensory system and it affects around 1 in 4 diabetic patients in the UK. The purpose of this genome-wide association study (GWAS) was to identify genetic contributors to this disorder. Cases of neuropathic pain were defined as diabetic patients with a multiple prescription history of at least one of five drugs specifically indicated for the treatment of neuropathic pain. Controls were diabetic individuals who were not prescribed any of these drugs, nor amitriptyline, carbamazepine, or nortriptyline. Overall, 961 diabetic neuropathic pain cases and 3260 diabetic controls in the Genetics of Diabetes Audit and Research Tayside (GoDARTS) cohort were identified. We found a cluster in the Chr1p35.1 (ZSCAN20-TLR12P) with a lowest P value of 2.74 x 10(-7) at rs71647933 in females and a cluster in the Chr8p23.1, next to HMGB1P46 with a lowest P value of 8.02 x 10(-7) at rs6986153 in males. Sex-specific narrow sense heritability was higher in males (30.0%) than in females (14.7%). This GWAS on diabetic neuropathic pain provides evidence for the sex-specific involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) with the disorder, indicating the need for further research. (C) 2015 The Authors. Published by Elsevier B.V.
引用
收藏
页码:1386 / 1393
页数:8
相关论文
共 64 条
[1]   Prevalence and Characteristics of Painful Diabetic Neuropathy in a Large Community-Based Diabetic Population in the UK [J].
Abbott, Caroline A. ;
Malik, Rayaz A. ;
van Ross, Ernest R. E. ;
Kulkarni, Jai ;
Boulton, Andrew J. M. .
DIABETES CARE, 2011, 34 (10) :2220-2224
[2]   EFNS guidelines on the pharmacological treatment of neuropathic pain: 2010 revision [J].
Attal, N. ;
Cruccu, G. ;
Baron, R. ;
Haanpaa, M. ;
Hansson, P. ;
Jensen, T. S. ;
Nurmikko, T. .
EUROPEAN JOURNAL OF NEUROLOGY, 2010, 17 (09) :1113-E88
[3]   Epidemiology, public health burden, and treatment of diabetic peripheral neuropathic pain: A review [J].
Barrett, Amy M. ;
Lucero, Melanie A. ;
Le, Trong ;
Robinson, Rebecca L. ;
Dworkin, Robert H. ;
Chappell, Amy S. .
PAIN MEDICINE, 2007, 8 :S50-S62
[4]   Haploview: analysis and visualization of LD and haplotype maps [J].
Barrett, JC ;
Fry, B ;
Maller, J ;
Daly, MJ .
BIOINFORMATICS, 2005, 21 (02) :263-265
[5]   TLR7 Ligands induce higher IFN-α production in females [J].
Berghofer, Beate ;
Frommer, Ture ;
Haley, Gabriela ;
Fink, Ludger ;
Bein, Gregor ;
Hackstein, Holger .
JOURNAL OF IMMUNOLOGY, 2006, 177 (04) :2088-2096
[6]   Glial TLR4 receptor as new target to treat neuropathic pain: Efficacy of a new receptor antagonist in a model of peripheral nerve injury in mice [J].
Bettoni, Isabella ;
Comelli, Francesca ;
Rossini, Clara ;
Granucci, Francesca ;
Giagnoni, Gabriella ;
Peri, Francesco ;
Costa, Barbara .
GLIA, 2008, 56 (12) :1312-1319
[7]   Enhanced glucose control for preventing and treating diabetic neuropathy [J].
Callaghan, B. C. ;
Little, A. A. ;
Feldman, E. L. ;
Hughes, R. A. C. .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2012, (06)
[8]   Disruption of the P2X7 purinoceptor gene abolishes chronic inflammatory and neuropathic pain [J].
Chessell, IP ;
Hatcher, JP ;
Bountra, C ;
Michel, AD ;
Hughes, JP ;
Green, P ;
Egerton, J ;
Murfin, M ;
Richardson, J ;
Peck, WL ;
Grahames, CBA ;
Casula, MA ;
Yiangou, Y ;
Birch, R ;
Anand, P ;
Buell, GN .
PAIN, 2005, 114 (03) :386-396
[9]   Pseudogene-mediated posttranscriptional silencing of HMGA1 can result in insulin resistance and type 2 diabetes [J].
Chiefari, Eusebio ;
Iiritano, Stefania ;
Paonessa, Francesco ;
Le Pera, Ilaria ;
Arcidiacono, Biagio ;
Filocamo, Mirella ;
Foti, Daniela ;
Liebhaber, Stephen A. ;
Brunetti, Antonio .
NATURE COMMUNICATIONS, 2010, 1
[10]  
Cook-Sather S.D., 2014, PAIN, V155, P1383