Department of Medicine, University of Pittsburgh, Room 401.4, 3708 Fifth Ave, Pittsburgh, PA, 15213, USA.
Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
J Gastroenterol. 2020 Oct;55(10):1000-1009. doi: 10.1007/s00535-020-01703-w. Epub 2020 Jul 17.
Pain is the most debilitating symptom of recurrent acute pancreatitis (RAP) and chronic pancreatitis (CP) and often requires chronic opioids or total pancreatectomy with islet autotransplantation to manage. Pain is a complex experience that can be exacerbated by depression and vice versa. Our aim was to test the hypothesis that depression-associated genes are associated with a constant-severe pain experience in RAP/CP patients.
A retrospective study was done using North American Pancreatitis Study II (NAPS2) genotyped RAP and CP patients with completed case report forms (n = 1,357). Subjects were divided based on pattern of pain and pain severity as constant-severe pain (n = 787) versus not constant-severe pain (n = 570) to conduct a nested genome-wide association study. The association between reported antidepressant medication use and depression gene loci was tested.
Constant-severe pain was reported in 58% (n = 787) of pancreatitis patients. No differences in sex or alcohol consumption were found based on pain severity. Antidepressant use was reported in 28% (n = 223), and they had lower SF-12 mental quality of life (MCS, p < 2.2 × 10). Fifteen loci associated with constant-severe pain (p < 0.00001) were found to be in or near depression-associated genes including ROBO2, CTNND2, SGCZ, CNTN5 and BAIAP2. Three of these genes respond to antidepressant use (SGCZ, ROBO2, and CTNND2).
Depression is a major co-factor in the pain experience. This genetic predisposition to depression may have utility in counseling patients and in instituting early antidepressant therapy for pain management of pancreatitis patients. Prospective randomized trials are warranted.
Clinicaltriasl.gov.# NCT01545167.
疼痛是复发性急性胰腺炎(RAP)和慢性胰腺炎(CP)最使人虚弱的症状,通常需要长期使用阿片类药物或全胰切除术伴胰岛自体移植来治疗。疼痛是一种复杂的体验,可能会因抑郁而加重,反之亦然。我们的目的是检验这样一个假设,即与抑郁相关的基因与 RAP/CP 患者的持续严重疼痛体验有关。
使用北美胰腺炎研究 II(NAPS2)进行了一项回顾性研究,对已完成病例报告表的 RAP 和 CP 患者进行了基因分型(n=1357)。根据疼痛模式和疼痛严重程度将受试者分为持续严重疼痛(n=787)和非持续严重疼痛(n=570),进行巢式全基因组关联研究。检验了报告的抗抑郁药物使用与抑郁基因座之间的关联。
58%(n=787)的胰腺炎患者报告有持续严重的疼痛。疼痛严重程度与性别或饮酒无差异。报告使用抗抑郁药的有 28%(n=223),他们的 SF-12 心理健康量表(MCS)评分较低(p<2.2×10)。发现 15 个与持续严重疼痛相关的基因座(p<0.00001)位于或靠近与抑郁相关的基因内,包括 ROBO2、CTNND2、SGCZ、CNTN5 和 BAIAP2。其中三个基因对抗抑郁药有反应(SGCZ、ROBO2 和 CTNND2)。
抑郁是疼痛体验的主要伴随因素。这种对抑郁的遗传易感性可能有助于为患者提供咨询,并为胰腺炎患者的疼痛管理实施早期抗抑郁治疗。需要进行前瞻性随机试验。
Clinicaltrials.gov# NCT01545167。