School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; NeuroImaging Network (NIN), Universal Scientific Education and Research Network (USERN), Tehran University of Medical Sciences, Tehran, Iran.
Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran; MetaCognition Interest Group (MCIG), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
Sleep Med. 2021 May;81:268-284. doi: 10.1016/j.sleep.2021.02.040. Epub 2021 Feb 24.
Narcolepsy, a sleep disorder characterized by loss of hypocretin neurons, has been associated with metabolic disturbances. Although the metabolic alterations in narcolepsy patients are widely investigated in the literature, the results are controversial. We performed a systematic search of literature to identify metabolic profiling studies in narcolepsy patients. A total of 48 studies were included in the meta-analysis. Narcolepsy patients exhibited higher prevalence of obesity (log OR = 0.93 [0.73-1.13], P < 0.001), diabetes mellitus (log OR = 0.64 [0.34, 0.94], P < 0.001), hypertension (log OR = 0.33 [0.11, 0.55], P < 0.001), and dyslipidemia (log OR = 1.19 [0.60, 1.77], P < 0.001) compared with non-narcoleptic controls. Narcolepsy was associated with higher BMI (SMD = 0.50 [0.32-0.68], P < 0.001), waist circumference (MD = 8.61 [2.03-15.19], P = 0.01), and plasma insulin (SMD = 0.61 [0.14-1.09], P = 0.01). Levels of fasting blood glucose (SMD = -0.25 [-0.61,0.10], P = 0.15), BMR-RMR (SMD = -0.17 [-0.52-0.18], P = 0.34), systolic blood pressure (SMD = 0.29 [-0.39-0.97], P = 0.40), diastolic blood pressure (SMD = 0.39 [-0.62, 1.40], P = 0.45), CSF melanin-concentrating hormone (MD = 5.56 [-30.79-41.91], P = 0.76), serum growth hormone (SMD = 7.84 [-7.90-23.57], P = 0.33), as well as plasma and CSF leptin (SMD = 0.10 [-1.32-1.51], P = 0.89 and MD = 0.01 [-0.02-0.04], P = 0.56, respectively) did not significantly differ between narcolepsy patients and controls. These findings necessitate early screening of metabolic alterations and cardiovascular risk factors in narcolepsy patients to reduce the morbidity and mortality rates.
发作性睡病是一种以下丘脑分泌素神经元缺失为特征的睡眠障碍性疾病,与代谢紊乱有关。尽管发作性睡病患者的代谢改变在文献中得到了广泛研究,但结果存在争议。我们进行了系统性文献检索,以确定发作性睡病患者的代谢谱研究。共有 48 项研究纳入荟萃分析。与非发作性睡病对照组相比,发作性睡病患者肥胖(优势比 [OR] = 0.93 [0.73-1.13],P < 0.001)、糖尿病(OR = 0.64 [0.34-0.94],P < 0.001)、高血压(OR = 0.33 [0.11-0.55],P < 0.001)和血脂异常(OR = 1.19 [0.60-1.77],P < 0.001)的患病率更高。发作性睡病与更高的 BMI(标准化均数差 [SMD] = 0.50 [0.32-0.68],P < 0.001)、腰围(MD = 8.61 [2.03-15.19],P = 0.01)和血浆胰岛素(SMD = 0.61 [0.14-1.09],P = 0.01)有关。空腹血糖(SMD = -0.25 [-0.61,0.10],P = 0.15)、BMR-RMR(SMD = -0.17 [-0.52-0.18],P = 0.34)、收缩压(SMD = 0.29 [-0.39-0.97],P = 0.40)、舒张压(SMD = 0.39 [-0.62,1.40],P = 0.45)、脑脊液黑素细胞刺激素(MD = 5.56 [-30.79-41.91],P = 0.76)、血清生长激素(SMD = 7.84 [-7.90-23.57],P = 0.33)以及血浆和脑脊液瘦素(SMD = 0.10 [-1.32-1.51],P = 0.89 和 MD = 0.01 [-0.02-0.04],P = 0.56)在发作性睡病患者和对照组之间没有显著差异。这些发现需要对发作性睡病患者进行早期代谢改变和心血管危险因素筛查,以降低发病率和死亡率。