Arnulf Isabelle, Lin Ling, Zhang Jing, Russell I Jon, Ripley Beth, Einen Mali, Nevsimalova Sonia, Bassetti Claudio, Bourgin Patrice, Nishino Seiji, Mignot Emmanuel
Center for Narcolepsy, Department of Psychiatry and Behavioral Sciences, Stanford University, Palo Alto, CA, USA.
Sleep. 2006 Aug;29(8):1017-24. doi: 10.1093/sleep/29.8.1017.
To determine if hypocretin deficiency is associated with abnormally low serum leptin levels, a putative cause of increased body mass index in narcoleptics.
Cross-sectional controlled study.
Three hundred seventy subjects, including 111 healthy controls, 93 narcoleptic subjects with hypocretin deficiency (cerebrospinal fluid [CSF] hypocretin-1 levels < 110 pg/mL), 72 narcoleptic subjects with normal hypocretin levels, and 89 subjects with other sleep disorders
After completing the Stanford Sleepiness Inventory, participants underwent spinal taps and blood sampling for measurement of CSF leptin and hypocretin-1 levels, HLA DQB1*0602 phenotyping, and serum leptin and C-reactive protein levels.
Serum leptin levels were similar in narcoleptic subjects, whether hypocretin-deficient (13.2 +/- 1.7 ng/mL, mean +/- SEM) or not (13.0 +/- 1.8 ng/mL), controls (10.1 +/- 1.1 ng/mL) and subjects with other sleep disorders (11.5 +/- 1.6 ng/mL). Similarly, the CSF leptin levels and the CSF: serum leptin ratios (an indicator of brain leptin uptake) were not different between groups. Serum and CSF leptin levels were higher in women and in subjects with higher body mass indexes. Leptin brain uptake decreased in women, in the aged, and in more-obese subjects. In contrast with a presumed inhibitory effect of leptin on hypocretin-containing cells, CSF leptin levels tended to correlate positively with CSF hypocretin-1 levels. C-reactive protein was higher (4.2 +/- 0.9 mg/L) in narcoleptic subjects with hypocretin deficiency than in controls (1.4 +/- 0.3 mg/L, p = .0055), a difference still significant after adjustment on confounding factors.
Our data do not support a role for leptin in mediating increased body mass index in narcolepsy. A moderate but selective increase in C-reactive protein in hypocretin-1 deficient subjects should prompt research on inflammation in narcolepsy.
确定下丘脑分泌素缺乏是否与血清瘦素水平异常降低相关,血清瘦素水平异常降低被认为是发作性睡病患者体重指数增加的原因。
横断面对照研究。
370名受试者,包括111名健康对照者、93名下丘脑分泌素缺乏的发作性睡病患者(脑脊液[CSF]下丘脑分泌素-1水平<110 pg/mL)、72名下丘脑分泌素水平正常的发作性睡病患者以及89名患有其他睡眠障碍的受试者。
完成斯坦福嗜睡量表后,参与者接受腰椎穿刺和血液采样,以测量脑脊液瘦素和下丘脑分泌素-水平、HLA DQB1*0602基因分型以及血清瘦素和C反应蛋白水平。
发作性睡病患者的血清瘦素水平相似,无论是否存在下丘脑分泌素缺乏(分别为13.2±1.7 ng/mL,均值±标准误)或正常(13.0±1.8 ng/mL),对照组(10.1±1.1 ng/mL)和患有其他睡眠障碍的受试者(11.5±1.6 ng/mL)。同样,各组间脑脊液瘦素水平以及脑脊液:血清瘦素比值(脑内瘦素摄取的指标)并无差异。女性以及体重指数较高的受试者的血清和脑脊液瘦素水平更高。女性、老年人以及肥胖程度更高者的脑内瘦素摄取减少。与瘦素对含下丘脑分泌素细胞的假定抑制作用相反,脑脊液瘦素水平倾向于与脑脊液下丘脑分泌素-1水平呈正相关。下丘脑分泌素缺乏的发作性睡病患者的C反应蛋白水平(4.2±0.9 mg/L)高于对照组(1.4±0.3 mg/L,p = 0.0055),在对混杂因素进行校正后,差异仍然显著。
我们的数据不支持瘦素在介导发作性睡病患者体重指数增加中发挥作用。下丘脑分泌素-1缺乏患者的C反应蛋白有中度但选择性的升高,这应促使对发作性睡病中的炎症进行研究。