Pediatrics Research Group, Girona Institute for Biomedical Research, Girona, Spain.
Int J Obes (Lond). 2013 Feb;37(2):182-7. doi: 10.1038/ijo.2012.27. Epub 2012 Mar 6.
Shorter sleep duration predisposes to obesity, but the mechanisms whereby sleep deprivation affects body weight are poorly understood. We tested whether this association is modulated by the obesity genes FTO, TMEM18 and NRXN3.
Body mass index (BMI), waist circumference, visceral fat (abdominal ultrasound), homeostasis model assessment for insulin resistance (HOMA-IR), systolic blood pressure (SBP) and sleep time per 24 h were assessed in 297 asymptomatic children (151 boys, 146 girls; age range 5-9 years; BMI s.d. score range -2.0-4.0). Associations between sleep duration and the abovementioned outcomes were tested for three common single-nucleotide polymorphisms (SNPs), namely FTO (rs9939609), TMEM 18 (rs4854344) and NRXN3 (rs10146997), as well as for their combination.
TT homozygotes (but not A(*) carriers) for the FTO SNP, exhibited nominal associations between decreasing sleep duration and increasing BMI, waist circumference, visceral fat and HOMA-IR (all P<0.05). Similar associations were observed in children with risk alleles (but not in those without risk alleles) for the TMEM18 and NRXN3 SNPs (P<0.05 to P<0.0001). The three SNPs had additive effects on the negative associations between sleep and, respectively, BMI (P<0.001), waist (P<0.005), visceral fat (P<0.001), HOMA-IR (P=0.010) and SBP (P<0.0005). The combined effects on obesity measures and SBP remained significant after correction for multiple testing. On average, 2 h of sleep less per night was associated with an increase in BMI of 1.0 s.d. (95% confidence interval 0.5-1.6 s.d.) and with 8.0 cm (95% confidence interval 3.6-12.2 cm) more waist circumference in genetically susceptible children.
By age 7, common variations in FTO, TMEM18 and NRXN3 influence the vulnerability to metabolic complications of sleep deprivation. Further genetic studies are warranted to replicate these findings in other populations.
睡眠时间较短会导致肥胖,但睡眠不足影响体重的机制尚不清楚。我们检测了这种关联是否受肥胖基因 FTO、TMEM18 和 NRXN3 的调节。
297 名无症状儿童(男 151 名,女 146 名;年龄 5-9 岁;体重指数标准差评分范围-2.0-4.0)接受了体重指数(BMI)、腰围、内脏脂肪(腹部超声)、胰岛素抵抗稳态模型评估(HOMA-IR)、收缩压(SBP)和 24 小时睡眠时间的评估。测试了三种常见的单核苷酸多态性(SNP),即 FTO(rs9939609)、TMEM18(rs4854344)和 NRXN3(rs10146997),以及它们的组合与睡眠时间之间的关系。
FTO SNP 的 TT 纯合子(而非 A(*)携带者)与睡眠时间减少和 BMI、腰围、内脏脂肪和 HOMA-IR 增加之间存在名义关联(所有 P<0.05)。在 TMEM18 和 NRXN3 SNP 的风险等位基因儿童中也观察到类似的关联(但在没有风险等位基因的儿童中没有)(P<0.05 至 P<0.0001)。三个 SNP 对睡眠与 BMI(P<0.001)、腰围(P<0.005)、内脏脂肪(P<0.001)、HOMA-IR(P=0.010)和 SBP(P<0.0005)之间的负相关具有相加效应。经过多次检验校正后,对肥胖指标和 SBP 的联合影响仍然显著。平均而言,每晚睡眠时间减少 2 小时与 BMI 增加 1.0 s.d.(95%置信区间 0.5-1.6 s.d.)和腰围增加 8.0 cm(95%置信区间 3.6-12.2 cm)有关在遗传易感儿童中。
在 7 岁时,FTO、TMEM18 和 NRXN3 的常见变异影响了睡眠剥夺导致代谢并发症的易感性。需要进一步的遗传研究来复制这些在其他人群中的发现。