CACNG2 polymorphisms associate with chronic pain after mastectomy

被引:18
作者
Bortsov, Andrey, V [1 ]
Devor, Marshall [2 ,3 ]
Kaunisto, Man A. [4 ]
Kalso, Eija [5 ]
Brufsky, Adam [6 ]
Kehlet, Henrik [7 ]
Aasvang, Eske [7 ]
Bittner, Reinhard [8 ]
Diatchenko, Luda [9 ]
Belfer, Inna [10 ]
机构
[1] Duke Univ, Dept Anesthesiol, Ctr Translat Pain Med, Durham, NC USA
[2] Hebrew Univ Jerusalem, Inst Life Sci, Dept Cell & Dev Biol, Jerusalem, Israel
[3] Hebrew Univ Jerusalem, Ctr Res Pain, Jerusalem, Israel
[4] Univ Helsinki, Inst Mol Med Finland FIMM, Helsinki Inst Life Sci, Helsinki, Finland
[5] Univ Helsinki, Helsinki Univ Hosp, Dept Perioperat Intens Care & Pain Med, Helsinki, Finland
[6] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
[7] Univ Copenhagen, Rigshosp, Sect Surg Pathophysiol, Copenhagen, Denmark
[8] Marienhosp Stuttgart, Ctr Minimal Invas Surg, Dept Gen & Visceral Surg, Stuttgart, Germany
[9] McGill Univ, Alan Edwards Ctr Res Pain, Montreal, PQ, Canada
[10] NIH, Bldg 10, Bethesda, MD 20892 USA
关键词
Breast cancer; CACNG2; Neuropathic pain; Pain genetics; Mastectomy pain; Postsurgical pain; POSTMASTECTOMY PAIN; NEUROPATHIC PAIN; STARGAZIN; SEX; SUSCEPTIBILITY; PREVALENCE; MODULATION; RECEPTORS; MECHANISM; GENETICS;
D O I
10.1097/j.pain.0000000000001432
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Chronic postmastectomy pain (PMP) imposes a major burden on the quality of life of the ever-increasing number of long-term survivors of breast cancer. An earlier report by Nissenbaum et al. claimed that particular polymorphisms in the gene CACNG2 are associated with the risk of developing chronic PMP after breast surgery (Nissenbaum J, Devor M, Settzer Z, Gebauer M, Michaelis M, Tal M, Dorfman R, Abitbul-Yarkoni M, Lu Y, Elahipanah T, delCanho 5, Minert A, Fried K, Persson AK, Shpigler H, Shabo E, Yakir B, Pisante A, Darvasi A. Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2. Genome Res 2010;20: 1180-90). This information is important because in principle, it can inform the surgical, radiological, and chemotherapeutic decision-making process in ways that could mitigate the increased risk of chronic pain. In this study, we revisited this claim by independently evaluating the proposed marker haplotype using 2 different patient cohorts recruited in different research settings. Meta-analysis of these new postmastectomy cohorts and the original cohort confirmed significant association of the CACNG2 haplotype with PMP. In addition, we tested whether the same markers would predict chronic postsurgical pain in men who underwent surgery for inguinal hernia repair, and whether there is significant genetic association with cutaneous thermal sensitivity in postmastectomy and postherniotomy patients. We found that the biomarker is selective because it did not predict pain after laparoscopic hernia repair and was not associated with pain sensitivity to experimentally applied noxious thermal stimuli. We conclude that the A-C-C haplotype at the 3 single-nucleotide polymorphisms (rs4820242, rs2284015, and rs2284017) in the CACNG2 gene is associated with increased risk of developing PMP. This information may advance current knowledge on pathophysiology of PMP and serve as a step forward in the prediction of clinical outcomes and personalized pain management.
引用
收藏
页码:561 / 568
页数:8
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