Department of Maternal and Child Health Care, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, 13 Hangkong Road, Wuhan, Hubei, China.
Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, 100 Hongkong Road, Wuhan, Hubei, China.
Biomed Res Int. 2022 Mar 7;2022:1499454. doi: 10.1155/2022/1499454. eCollection 2022.
Childhood overweight and obesity (OW/OB) is a worldwide public health problem, and its genetic risks remain unclear.
To investigate risks of OW/OB associated with genetic variances in rs543874 and rs10913469, rs11030104 and rs6265, rs11191580, rs11165675, rs2531995, rs7869969, rs2237892, and rs2968990 in Chinese infants at 12-month old.
We conducted a case-control study with 734 infants included at delivery and followed up to 12-month old. The classification and regression tree analysis were used to generate the structure of the gene-gene interactions, while the unconditional multivariate logistic regression models were applied to analyze the single SNP, gene-gene interactions, and cumulative effects of the genotypes on OW/OB, adjusted for potential confounders.
There were 219 (29.84%) OW/OB infants. Rs543874 G allele and rs11030104 AA genotype increased the risk of OW/OB in 12-month-old infants ( < 0.05). Those carrying both rs11030104 AA genotype and rs10913469 C allele had 4.3 times greater OW/OB than those carrying rs11030104 G allele, rs11191580 C allele, rs11165675 A allele, and rs543874 AA genotype. Meanwhile, the risk of OW/OB increased with the number of the risk genotypes individuals harbored.
Rs543874, rs11030104, and rs11191580 were associated with OW/OB in 12-month-old Chinese infants, and the three SNPs together with rs10913469 and rs11165675 had a combined effect on OW/OB.
儿童超重和肥胖(OW/OB)是一个全球性的公共卫生问题,但其遗传风险尚不清楚。
探究 rs543874 和 rs10913469、rs11030104 和 rs6265、rs11191580、rs11165675、rs2531995、rs7869969、rs2237892 和 rs2968990 这 5 个基因座上的遗传变异与中国 12 个月大婴儿 OW/OB 相关的风险。
我们开展了一项病例对照研究,纳入了 734 名分娩婴儿,并随访至 12 个月。采用分类回归树分析生成基因-基因相互作用结构,采用无条件多变量逻辑回归模型分析单核苷酸多态性、基因-基因相互作用以及基因型对 OW/OB 的累积效应,同时调整潜在混杂因素。
共有 219 名(29.84%)婴儿为 OW/OB。rs543874 的 G 等位基因和 rs11030104 的 AA 基因型增加了 12 个月大婴儿 OW/OB 的风险(<0.05)。同时携带 rs11030104 的 AA 基因型和 rs10913469 的 C 等位基因的婴儿与携带 rs11030104 的 G 等位基因、rs11191580 的 C 等位基因、rs11165675 的 A 等位基因和 rs543874 的 AA 基因型的婴儿相比,OW/OB 的风险增加了 4.3 倍。此外,个体携带的风险基因型数量越多,OW/OB 的风险就越高。
rs543874、rs11030104 和 rs11191580 与中国 12 个月大婴儿的 OW/OB 相关,rs11030104、rs11191580、rs543874、rs10913469 和 rs11165675 这 5 个 SNPs 联合作用对 OW/OB 有影响。