Department of Nursing, International Institutes of Medicine, The Fourth Affiliated Hospital, Zhejiang University School of Medicine, Yiwu, Zhejiang, China.
Department of Biobehavioral Sciences, Teachers College-Columbia University, New York, NY, United States of America.
PLoS One. 2024 Mar 8;19(3):e0300074. doi: 10.1371/journal.pone.0300074. eCollection 2024.
Observational studies have suggested associations between sedentary behaviors (SB), physical activity (PA), sleep duration (SD), and obesity, but the causal relationships remain unclear.
We used Mendelian randomization (MR) with genetic variation as instrumental variables (IVs) to assess the causality between SB/PA/SD and obesity. Genetic variants associated with SB/PA/SD were obtained from Genome-wide association study (GWAS), and obesity data came from FinnGen. The primary MR analysis used the instrumental variable weighted (IVW) method, with sensitivity tests including Cochran Q, MR-Egger intercepts, and MR-Radial. Expression Quantitative Trait Loci (eQTL) analysis was applied to identify significant genetic associations and biological pathways in obesity-related tissues.
The MR analysis revealed causal relationships between four SB-related lifestyle patterns and obesity. Specifically, increased genetic liability to television watching (IVW MR Odds ratio [OR] = 1.55, [95% CI]:[1.27, 1.90], p = 1.67×10-5), computer use ([OR] = 1.52, [95% CI]:[1.08, 2.13], p = 1.61×10-2), leisure screen time (LST) ([OR] = 1.62, [95% CI] = [1.43, 1.84], p = 6.49×10-14, and driving (MR [OR] = 2.79, [95% CI]:[1.25, 6.21], p = 1.23×10-2) was found to increase the risk of obesity. Our findings indicate that no causal relationships were observed between SB at work, sedentary commuting, PA, SD, and obesity. The eQTL analysis revealed strong associations between specific genes (RPS26, TTC12, CCDC92, NICN1) and SNPs (rs10876864, rs2734849, rs4765541, rs7615206) in both subcutaneous and visceral adipose tissues, which are associated with these SBs. Enrichment analysis further revealed that these genes are involved in crucial biological pathways, including cortisol synthesis, thyroid hormone synthesis, and insulin secretion.
Our findings support a causal relationship between four specific SBs (LST, television watching, computer use, driving) and obesity. These results provide valuable insights into potential interventions to address obesity effectively, supported by genetic associations in the eQTL and enrichment analysis. Further research and public health initiatives focusing on reducing specific SBs may be warranted.
观察性研究表明,久坐行为(SB)、体力活动(PA)、睡眠持续时间(SD)与肥胖之间存在关联,但因果关系尚不清楚。
我们使用孟德尔随机化(MR)方法,利用遗传变异作为工具变量(IVs),评估 SB/PA/SD 与肥胖之间的因果关系。与 SB/PA/SD 相关的遗传变异来自全基因组关联研究(GWAS),肥胖数据来自 FinnGen。主要的 MR 分析采用工具变量加权(IVW)法,敏感性测试包括 Cochran Q、MR-Egger 截距和 MR-Radial。表达数量性状基因座(eQTL)分析用于鉴定肥胖相关组织中具有显著遗传关联和生物学途径的基因。
MR 分析显示,四种与 SB 相关的生活方式与肥胖之间存在因果关系。具体而言,看电视(IVW MR 比值比[OR] = 1.55,[95%CI]:[1.27, 1.90],p = 1.67×10-5)、使用电脑(OR = 1.52,[95%CI]:[1.08, 2.13],p = 1.61×10-2)、休闲屏幕时间(LST)(OR = 1.62,[95%CI] = [1.43, 1.84],p = 6.49×10-14)和驾驶(MR [OR] = 2.79,[95%CI]:[1.25, 6.21],p = 1.23×10-2)与肥胖风险增加有关。我们的发现表明,在工作中 SB、久坐通勤、PA、SD 与肥胖之间没有观察到因果关系。eQTL 分析揭示了特定基因(RPS26、TTC12、CCDC92、NICN1)和 SNP(rs10876864、rs2734849、rs4765541、rs7615206)之间的强烈关联,这些基因与这些 SBs 相关。富集分析进一步表明,这些基因参与了皮质醇合成、甲状腺激素合成和胰岛素分泌等关键生物学途径。
我们的研究结果支持四个特定的 SB(LST、看电视、使用电脑、驾驶)与肥胖之间存在因果关系。这些结果为通过 eQTL 和富集分析中的遗传关联有效解决肥胖问题提供了有价值的见解。进一步的研究和关注减少特定 SB 的公共卫生措施可能是必要的。