Li Song, Toneman Masja K, Mangnus Judith P M, Strocchi Stefano, van Boekel Regina L M, Vissers Kris C P, Ten Broek Richard P G, Coenen Marieke J H
Department of Human Genetics, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Department of Surgery, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Anaesthesia. 2025 May;80(5):499-510. doi: 10.1111/anae.16528. Epub 2024 Dec 29.
Chronic pain is one of the most common and severe complications after surgery, affecting quality of life and overall wellbeing of patients. Several risk factors have been identified but the mechanisms of chronic postsurgical pain development remain unclear. This study aimed to identify single-nucleotide polymorphisms associated with developing chronic postsurgical pain after abdominal surgery, one of the most common types of surgery.
A genome-wide association study was performed on 27,603 patients from the UK Biobank who underwent abdominal surgery. The robustness of identified loci was validated by split-half validation analysis. Functionally related top loci were selected for expression validation in clinical samples of adhesions from patients with and without pain.
One locus (rs185545327) reached genome-wide significance for association with chronic postsurgical pain development, and 10 loci surpassed the suggestively significant threshold (p < 1 × 10). In the robustness analysis, eight loci had at least nominal significance. The loci passing the suggestively significant threshold were mapped to 15 genes, of which two loci contained pain-related genes (SRPK2, PDE4D). Although marginally approaching statistical significance in the expression validation of clinical samples, the detection rate and expression level of PDE4D were modestly higher in patients with pain compared with those in the control group.
This study provides preliminary evidence for genetic risk factors implicated in chronic postsurgical pain following abdominal surgery, particularly the PDE4D gene, which has been associated with pain in previous studies. The findings add to evidence suggesting potential for the future development of a clinically applicable tool for personalised risk prediction, aiding clinicians in stratifying patients and enhancing clinical decision-making through individualised risk assessments.
慢性疼痛是手术后最常见且严重的并发症之一,影响患者的生活质量和整体健康状况。虽然已确定了多个风险因素,但慢性术后疼痛的发生机制仍不清楚。本研究旨在确定与腹部手术(最常见的手术类型之一)后发生慢性术后疼痛相关的单核苷酸多态性。
对来自英国生物银行的27603例接受腹部手术的患者进行了全基因组关联研究。通过对半验证分析验证所确定位点的稳健性。选择功能相关的顶级位点在有疼痛和无疼痛患者的粘连临床样本中进行表达验证。
一个位点(rs185545327)与慢性术后疼痛的发生达到全基因组显著性关联,10个位点超过提示性显著阈值(p < 1×10)。在稳健性分析中,8个位点至少具有名义显著性。通过提示性显著阈值的位点被定位到15个基因,其中两个位点包含与疼痛相关的基因(SRPK2、PDE4D)。虽然在临床样本的表达验证中略接近统计学显著性,但与对照组相比,疼痛患者中PDE4D的检测率和表达水平略高。
本研究为腹部手术后慢性术后疼痛的遗传风险因素提供了初步证据,特别是PDE4D基因,该基因在先前的研究中已与疼痛相关。这些发现进一步证明了未来开发临床适用的个性化风险预测工具的潜力,有助于临床医生对患者进行分层,并通过个性化风险评估加强临床决策。