Tufts University School of Medicine, Boston, Massachusetts.
Division of Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
JAMA Netw Open. 2024 Sep 3;7(9):e2431949. doi: 10.1001/jamanetworkopen.2024.31949.
The gut-first hypothesis of Parkinson disease (PD) has gained traction, yet potential inciting events triggering Parkinson pathology from gut-related factors remain unclear. While Helicobacter pylori infection is linked to mucosal damage (MD) and PD, it is unknown how upper gastrointestinal MD from any source increases PD risk.
To evaluate any association between upper endoscopy findings of MD and subsequent clinical PD diagnosis.
DESIGN, SETTING, AND PARTICIPANTS: This was a retrospective cohort study of patients with no PD history undergoing upper endoscopy with biopsy between January 2000 and December 2005, with final follow-up assessments completed July 31, 2023. The study was conducted within the Mass General Brigham system, a multicenter network in the greater Boston, Massachusetts, area. Patients with MD were matched 1:3 to patients without MD based on age, sex, and date of initial endoscopy.
MD, defined as erosions, esophagitis, ulcers, or peptic injury, observed on upper endoscopy or pathology reports.
The relative risk of PD given a history of MD, estimated using incident rate ratio (IRR) and multivariate Cox proportional hazard ratios (HRs).
Of 9350 patients, participants had a mean (SD) age of 52.3 (20.3) years; 5177 (55.4%) were male; and 269 (2.9%) were Asian, 737 (7.9%) Black, and 6888 (73.7%) White. Most participants underwent endoscopy between the ages of 50 and 64 years (2842 [30.4%]). At baseline, patients with MD were more likely to have a history of H pylori infection, proton-pump inhibitor use, chronic nonsteroidal anti-inflammatory drug use, gastroesophageal reflux disease, smoking, constipation, and dysphagia. The mean (SD) follow-up time was 14.9 (6.9) years for the whole cohort, during which patients with MD were more likely to develop PD (IRR, 4.15; 95% CI, 2.89-5.97; P < .001) than those without MD, even after covariate adjustment (HR, 1.76; 95% CI 1.11-2.51; P = .01). Constipation, dysphagia, older age, and higher Charlson-Deyo Comorbidity Index were also associated with higher PD risk.
In this cohort study, a history of upper gastrointestinal MD was associated with elevated risk of developing a clinical PD diagnosis. Increased vigilance among patients with MD for future PD risk may be warranted.
肠道优先假说已被广泛接受,但仍不清楚肠道相关因素引发帕金森病(PD)病理的潜在触发因素。虽然幽门螺杆菌感染与黏膜损伤(MD)和 PD 有关,但尚不清楚任何来源的上消化道 MD 如何增加 PD 风险。
评估上消化道内镜检查 MD 结果与随后的临床 PD 诊断之间的任何关联。
设计、地点和参与者:这是一项回顾性队列研究,纳入了 2000 年 1 月至 2005 年 12 月期间无 PD 病史、接受上消化道内镜检查和活检的患者,最终随访评估于 2023 年 7 月 31 日完成。该研究在马萨诸塞州波士顿地区的大型综合医疗保健系统内进行,该系统是一个多中心网络。根据年龄、性别和首次内镜检查日期,将 MD 患者与无 MD 患者 1:3 匹配。
MD 定义为上消化道内镜检查或病理报告中观察到的糜烂、食管炎、溃疡或消化性损伤。
使用发病率比(IRR)和多变量 Cox 比例风险比(HR)估计 MD 病史下 PD 的相对风险。
在 9350 名患者中,参与者的平均(SD)年龄为 52.3(20.3)岁;5177 名(55.4%)为男性;269 名(2.9%)为亚洲人,737 名(7.9%)为黑人,6888 名(73.7%)为白人。大多数参与者在 50 至 64 岁之间接受内镜检查(2842 名[30.4%])。在基线时,MD 患者更有可能有幽门螺杆菌感染、质子泵抑制剂使用、慢性非甾体抗炎药使用、胃食管反流病、吸烟、便秘和吞咽困难的病史。整个队列的平均(SD)随访时间为 14.9(6.9)年,与无 MD 的患者相比,MD 患者更有可能发展为 PD(IRR,4.15;95%CI,2.89-5.97;P<0.001),即使在调整了协变量后也是如此(HR,1.76;95%CI 1.11-2.51;P=0.01)。便秘、吞咽困难、年龄较大和更高的 Charlson-Deyo 合并症指数也与更高的 PD 风险相关。
在这项队列研究中,上消化道 MD 史与 PD 临床诊断风险升高相关。对于 MD 患者,未来 PD 风险可能需要更高的警惕性。