Zehra Yavuz, Merve Uzun, Turay Mutlu, Gürkan Değirmencioğlu, Mehmet Hanifi Çanakçı, Dilek İşcan, Halil Önder, İsmet Murat Melek, Selim Selçuk Çomoğlu
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引用次数: 0
Abstract
Aims: Functional gastrointestinal disorders (FGIDs) are part of the non-motor spectrum of idiopathic Parkinson's disease (iPD). The prevalence and relevance of Rome IV-defined functional bowel disorders (FBDs) remain unclear. This study evaluated FBD prevalence and correlates in iPD using a gastroenterology-based control group.
Methods: This cross-sectional study included 64 iPD patients and 64 controls without neurological disease with Rome IV-defined FGIDs. FGIDs were assessed using the Rome IV Diagnostic Questionnaire. Non-motor symptoms, mood, and quality of life were evaluated using NMSS, Hamilton scales, PDQ-39, and GIQLI. Multivariable analyses were performed.
Results: FBD prevalence did not differ between iPD and the FGID-enriched control group (20.3% vs. 21.9%, p = 0.828; adjusted OR 0.83, 95% CI 0.23-2.95, p = 0.774). Within iPD, FBD positivity was associated with worse PDQ-39 scores and higher non-motor burden, particularly in attention/memory and sexual domains. Anxiety severity was negatively associated with GIQLI.
Conclusion: In this FGID-enriched comparison, FBD prevalence was not higher in iPD. However, FBDs were associated with greater non-motor burden and poorer quality of life. These findings suggest FGIDs may be associated with variation in the non-motor phenotype rather than disease risk. Interpretation should be cautious due to control selection and demographic imbalance.
目的:功能性胃肠疾病(fgid)是特发性帕金森病(iPD)非运动谱的一部分。罗马iv定义的功能性肠病(fbd)的患病率和相关性尚不清楚。本研究使用以胃肠病学为基础的对照组来评估FBD在iPD中的患病率及其相关因素。方法:这项横断面研究包括64名iPD患者和64名没有神经系统疾病的对照,并伴有罗马iv定义的FGIDs。fgid采用Rome IV诊断问卷进行评估。采用NMSS、Hamilton量表、PDQ-39和GIQLI评估非运动症状、情绪和生活质量。进行多变量分析。结果:FBD患病率在iPD和fgid富集对照组之间无差异(20.3% vs. 21.9%, p = 0.828;校正OR 0.83, 95% CI 0.23-2.95, p = 0.774)。在iPD中,FBD阳性与较差的PDQ-39评分和较高的非运动负担相关,特别是在注意/记忆和性领域。焦虑严重程度与GIQLI呈负相关。结论:在这个fgid富集的比较中,iPD中FBD的患病率并不高。然而,fbd与更大的非运动负担和更差的生活质量有关。这些发现表明,fgid可能与非运动表型的变异有关,而不是与疾病风险有关。由于对照选择和人口不平衡,解释应谨慎。