Concordance of Phantom and Residual Limb Pain Phenotypes in Double Amputees: Evidence for the Contribution of Distinct and Common Individual Factors

被引:14
作者
Streit, Fabian [1 ,4 ]
Bekrater-Bodmann, Robin [2 ]
Diers, Martin [2 ,5 ]
Reinhard, Iris [3 ]
Frank, Josef [1 ]
Wuest, Stefan [1 ,6 ]
Seltzer, Ze'ev [7 ,8 ,9 ]
Flor, Herta [2 ]
Rietschel, Marcella [1 ]
机构
[1] Heidelberg Univ, Med Fac Mannheim, Cent Inst Mental Hlth, Dept Genet Epidemiol Psychiat, Mannheim, Germany
[2] Heidelberg Univ, Med Fac Mannheim, Cent Inst Mental Hlth, Cognit & Clin Neurosci, Mannheim, Germany
[3] Heidelberg Univ, Med Fac Mannheim, Cent Inst Mental Hlth, Biostat, Mannheim, Germany
[4] Univ Trier, Inst Psychobiol, Trier, Germany
[5] Ruhr Univ Bochum, LWL Univ, Dept Psychosomat Med & Psychotherapy, Bochum, Germany
[6] Univ Regensburg, Inst Expt Psychol, D-93053 Regensburg, Germany
[7] Toronto Gen Hosp, Dept Anesthesia & Pain Management, Toronto, ON, Canada
[8] Univ Toronto, Fac Dent, Ctr Study Pain, Toronto, ON, Canada
[9] Univ Toronto, Fac Med, Ctr Study Pain, Toronto, ON, Canada
基金
欧洲研究理事会;
关键词
Phantom limb pain; residual limb pain; concordance; heritability of pain; multiple amputations; GENOME-WIDE ASSOCIATION; NEUROPATHIC PAIN; ENVIRONMENTAL-INFLUENCES; RISK-FACTORS; STUMP PAIN; HERITABILITY; PLASTICITY; METAANALYSIS; REPLICATION; SENSITIVITY;
D O I
10.1016/j.jpain.2015.08.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Most, but not all, limb amputees develop phantom limb pain (PLP) or residual limb pain (RIP), and large interindividual differences in pain intensity and course are apparent. The present cross-sectional study of 122 double amputees investigated the possible role of genetic factors in PLP and RLP, assuming that strong individual predisposition results in high intraindividual concordance in pain phenotype. Intraindividual concordance was observed in 116 (95%) patients for development of PLP and in 110 patients (90%) for development of RLR For both pain types, high intraindividual concordance was also observed for remission and current intensity. Moderate association for lifetime history and current intensity of PLP and RLP was observed both within and between limbs. The high intraindividual concordance in pain phenotypes suggests strong individual predisposition for PLP and RIP development. However, the finding of only moderate association between PLP and RIP suggests that susceptibility to these pain phenomena involves distinct, as well as common, risk factors. Genome-wide studies in large samples of single amputees may facilitate the dissection of these phenotypes and their underlying mechanisms. Perspective: The observation of high intraindividual concordance for PLP and RLP in 122 double amputees suggests that individual factors contribute to post-amputation pain. The relatively low intraindividual association between PLP and RLP suggests that these factors are at least partially specific for each pain type. (C) 2015 by the American Pain Society
引用
收藏
页码:1377 / 1385
页数:9
相关论文
共 52 条
[31]   Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood [J].
Lee, S. H. ;
Yang, J. ;
Goddard, M. E. ;
Visscher, P. M. ;
Wray, N. R. .
BIOINFORMATICS, 2012, 28 (19) :2540-2542
[32]   A genome-wide association study suggests an association of Chr8p21.3 (GFRA2) with diabetic neuropathic pain [J].
Meng, W. ;
Deshmukh, H. A. ;
van Zuydam, N. R. ;
Liu, Y. ;
Donnelly, L. A. ;
Zhou, K. ;
Morris, A. D. ;
Colhoun, H. M. ;
Palmer, C. N. A. ;
Smith, B. H. .
EUROPEAN JOURNAL OF PAIN, 2015, 19 (03) :392-399
[33]   Plasticity in human motor cortex is in part genetically determined [J].
Missitzi, Julia ;
Gentner, Reinhard ;
Geladas, Nickos ;
Politis, Panagiotis ;
Karandreas, Nikos ;
Classen, Joseph ;
Klissouras, Vassilis .
JOURNAL OF PHYSIOLOGY-LONDON, 2011, 589 (02) :297-306
[34]   Pain genetics: past, present and future [J].
Mogil, Jeffrey S. .
TRENDS IN GENETICS, 2012, 28 (06) :258-266
[35]   Heritability of nociception I: Responses of 11 inbred mouse strains on 12 measures of nociception [J].
Mogil, JS ;
Wilson, SG ;
Bon, K ;
Lee, SE ;
Chung, K ;
Raber, P ;
Pieper, JO ;
Hain, HS ;
Belknap, JK ;
Hubert, L ;
Elmer, GI ;
Chung, JM ;
Devor, M .
PAIN, 1999, 80 (1-2) :67-82
[36]   Twin studies of pain [J].
Nielsen, C. S. ;
Knudsen, G. P. ;
Steingrimsdottir, O. A. .
CLINICAL GENETICS, 2012, 82 (04) :331-340
[37]   Individual differences in pain sensitivity: Genetic and environmental contributions [J].
Nielsen, Christopher S. ;
Stubhaug, Audun ;
Price, Donald D. ;
Vassend, Olav ;
Czajkowski, Nikolai ;
Harris, Jennifer R. .
PAIN, 2008, 136 (1-2) :21-29
[38]   The influence of preamputation pain on postamputation stump and phantom pain [J].
Nikolajsen, L ;
Ilkjaer, S ;
Kroner, K ;
Christensen, JH ;
Jensen, TS .
PAIN, 1997, 72 (03) :393-405
[39]   Genome-wide association study identifies a potent locus associated with human opioid sensitivity [J].
Nishizawa, D. ;
Fukuda, K. ;
Kasai, S. ;
Hasegawa, J. ;
Aoki, Y. ;
Nishi, A. ;
Saita, N. ;
Koukita, Y. ;
Nagashima, M. ;
Katoh, R. ;
Satoh, Y. ;
Tagami, M. ;
Higuchi, S. ;
Ujike, H. ;
Ozaki, N. ;
Inada, T. ;
Iwata, N. ;
Sora, I. ;
Iyo, M. ;
Kondo, N. ;
Won, M-J ;
Naruse, N. ;
Uehara-Aoyama, K. ;
Itokawa, M. ;
Koga, M. ;
Arinami, T. ;
Kaneko, Y. ;
Hayashida, M. ;
Ikeda, K. .
MOLECULAR PSYCHIATRY, 2014, 19 (01) :55-62
[40]   pain2:: A neuropathic pain QTL identified on rat chromosome 2 [J].
Nissenbaum, Jonathan ;
Shpigler, Hagai ;
Pisante, Anne ;
delCanho, Sonia ;
Minert, Anne ;
Seltzer, Ze'ev ;
Devor, Marshall ;
Darvasi, Ariel .
PAIN, 2008, 135 (1-2) :92-97