Lee Hyo Jeong, Jung Kee Wook, Chung Sun Ju, Hong Seung-Mo, Kim Juyeon, Lee Jeong Hoon, Hwang Sung Wook, Ryu Ho-Sung, Kim Mi Jung, Lee Ho-Su, Seo Myeongsook, Park Sang Hyoung, Yang Dong-Hoon, Ye Byong Duk, Byeon Jeong-Sik, Choe Jaewon, Jung Hwoon-Yong, Yang Suk-Kyun, Myung Seung-Jae
Health Screening and Promotion Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Department of Gastroenterology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
J Neurogastroenterol Motil. 2018 Jul 30;24(3):469-478. doi: 10.5056/jnm17141.
BACKGROUND/AIMS: α-Synucleinopathy in the brain is the neuropathological hallmark of Parkinson's disease (PD). However, the functional impact of α-synucleinopathy in the enteric nervous system remains unknown. We aim to evaluate the association between gastrointestinal (GI) dysfunction and α-synuclein (αSYN) pathology in the stomach and colon of PD patients and controls, as well as to investigate the association between the αSYN pathology in GI tract and future PD risk.
A total of 35 PD patients and 52 neurologically intact subjects were enrolled in this study. Endoscopic biopsies were performed, and then immunohistochemical staining for αSYN was performed. All subjects completed the validated Rome III questionnaire for the assessment of GI symptoms. The association between GI symptoms and the αSYN pathology in GI mucosa was evaluated. Incident PD cases were assessed during a median follow-up of 46 months.
The proportion of self-reported constipation and functional constipation through the Rome III questionnaire was significantly higher in PD patients than in controls ( < 0.001 and = 0.015). However, no significant association was found between the αSYN pathology in the stomach and colon mucosa and constipation, as well as other GI symptoms including dyspepsia symptoms and abdominal discomfort or pain, regardless of the presence or absence of clinical PD ( > 0.05). No incident PD cases were diagnosed during study period.
Our present study suggests that the deposition of αSYN in the mucosal enteric nervous system may not be reflected by functional impairment of the affected segment of the gut.
背景/目的:大脑中的α-突触核蛋白病是帕金森病(PD)的神经病理学标志。然而,α-突触核蛋白病在肠神经系统中的功能影响仍不清楚。我们旨在评估PD患者和对照组胃和结肠中胃肠(GI)功能障碍与α-突触核蛋白(αSYN)病理学之间的关联,并研究胃肠道中αSYN病理学与未来PD风险之间的关联。
本研究共纳入35例PD患者和52例神经功能正常的受试者。进行内镜活检,然后进行αSYN免疫组织化学染色。所有受试者均完成了用于评估GI症状的经过验证的罗马III问卷。评估GI症状与GI黏膜中αSYN病理学之间的关联。在中位随访46个月期间评估新发PD病例。
通过罗马III问卷自我报告的便秘和功能性便秘的比例在PD患者中显著高于对照组(<0.001和=0.015)。然而,无论是否存在临床PD,胃和结肠黏膜中的αSYN病理学与便秘以及其他GI症状(包括消化不良症状和腹部不适或疼痛)之间均未发现显著关联(>0.05)。在研究期间未诊断出新发PD病例。
我们目前的研究表明,αSYN在黏膜肠神经系统中的沉积可能不会通过肠道受影响节段的功能损害反映出来。