Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Department of Neurology, Tianjin Huanhu Hospital, Tianjin, China.
Front Endocrinol (Lausanne). 2021 Nov 17;12:765701. doi: 10.3389/fendo.2021.765701. eCollection 2021.
Abnormal orexin-A levels in cerebrospinal fluid (CSF) have been identified in Alzheimer's disease (AD) and other neurodegenerative diseases. However, few studies have focused on Lewy body disease (LBD) and often with debatable outcomes. Thus, we performed this systematic review and meta-analysis to investigate orexin-A levels in LBD by incorporating data from different studies.
We gathered studies comparing orexin-A levels in patients with LBD and controls (including healthy controls and other dementia subtypes). In the initial search, 117 relevant articles were identified. After a selection process, seven studies, conducted in Japan, USA, Spain, Switzerland, France, Italy, and Netherlands, were chosen.
In total, 179 patients with LBD and 253 controls were included. Patients with LBD had significantly lower mean orexin-A CSF levels when compared with patients with AD [standard mean difference (SMD): -0.35, 95% confidence interval (CI): -0.70 to -0.00, Z = 1.96, P = 0.05], whereas mean orexin-A levels were significantly higher when compared with patients with frontotemporal lobar degeneration (FTLD) (SMD: 0.61, 95% CI: 0.23-0.99, Z = 3.12, P = 0.002). Orexin-A CSF levels in LBD patients were approximately equal to levels in healthy elderly individuals, whereas they were significantly decreased in LBD patients with excessive daytime sleepiness (EDS) (SMD: -0.15, 95% CI: -0.59 to 0.29, Z = 0.67, P = 0.50).
We showed that orexin-A levels in patients with LBD were not very different from those in normal elderly individuals, whereas they were lower than those in AD patients and higher than those in FTLD patients. The influence of hypersomnia on orexin-A levels should be carefully interpreted.
https://www.crd.york.ac.uk/prospero/, identifier CRD42021265900.
脑脊液(CSF)中异常的食欲素-A 水平已在阿尔茨海默病(AD)和其他神经退行性疾病中被确定。然而,很少有研究关注路易体病(LBD),并且结果往往存在争议。因此,我们进行了这项系统评价和荟萃分析,以通过整合来自不同研究的数据来研究 LBD 中的食欲素-A 水平。
我们收集了比较 LBD 患者和对照组(包括健康对照组和其他痴呆亚型)中食欲素-A 水平的研究。在最初的搜索中,确定了 117 篇相关文章。经过筛选过程,选择了来自日本、美国、西班牙、瑞士、法国、意大利和荷兰的七项研究。
总共纳入了 179 例 LBD 患者和 253 例对照组。与 AD 患者相比,LBD 患者的平均 CSF 食欲素-A 水平显著降低[标准均数差(SMD):-0.35,95%置信区间(CI):-0.70 至 -0.00,Z = 1.96,P = 0.05],而与额颞叶变性(FTLD)患者相比,平均食欲素-A 水平显著升高[SMD:0.61,95%CI:0.23-0.99,Z = 3.12,P = 0.002]。LBD 患者的 CSF 食欲素-A 水平与健康老年人的水平大致相当,而在有日间过度嗜睡(EDS)的 LBD 患者中,食欲素-A 水平显著降低[SMD:-0.15,95%CI:-0.59 至 0.29,Z = 0.67,P = 0.50]。
我们表明,LBD 患者的食欲素-A 水平与正常老年人的水平没有太大差异,而低于 AD 患者的水平,高于 FTLD 患者的水平。应仔细解释嗜睡对食欲素-A 水平的影响。
https://www.crd.york.ac.uk/prospero/,标识符 CRD42021265900。