Update on the genetics of the fibromyalgia syndrome

被引:71
作者
Ablin, Jacob N. [1 ,2 ]
Buskila, Dan [3 ,4 ]
机构
[1] Tel Aviv Sourasky Med Ctr, Inst Rheumatol, IL-64239 Tel Aviv, Israel
[2] Tel Aviv Univ, Sackler Sch Med, IL-69978 Tel Aviv, Israel
[3] Ben Gurion Univ Negev, Soroka Med Ctr, Dept Med H, IL-84105 Beer Sheva, Israel
[4] Ben Gurion Univ Negev, Fac Hlth Sci, Beer Sheva, Israel
来源
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2015年 / 29卷 / 01期
关键词
Centralized pain; Fibromyalgia; Neuropathic pain; T102C POLYMORPHISM; RECEPTOR GENE; RISK-FACTORS; PAIN; ASSOCIATION; FIBROSITIS; MICRORNAS; NEUROENDOCRINE; SENSITIVITY; HAPLOTYPES;
D O I
10.1016/j.berh.2015.04.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fibromyalgia syndrome (FMS), a condition characterized by chronic widespread pain and tenderness, is a complex condition considered to represent a paradigm of centralized pain. FMS has demonstrated a clear familial aggregation, and hence it is considered to have a genetic background. Multiple candidate-gene studies have been conducted in this field, focusing on target genes that play a role in the transmission and processing of pain. While many of these have focused in the past on markers related to neurotransmitter systems such as catecholamines (catechol-O-methyltransferase (COMT)) and serotonin, novel target genes have recently emerged. In addition, genome-wide sequencing scanning (genome-wide association study (GWAS)) is increasingly being harnessed for the study of chronic pain, including FMS. Micro RNAs are another novel field of research related to posttranscriptional inhibition of gene expression, which are currently regarding the pathogenesis of FMS. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:20 / 28
页数:9
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