Duque Abigail, Lin Jue, Jeliffe-Pawlowski Laura, Coleman-Phox Kim, Rand Larry, Wojcicki Janet M
Division of Pediatric Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, University of California San Francisco, San Francisco, California, USA.
Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, California, USA.
Pediatr Obes. 2025 Sep;20(9):e70034. doi: 10.1111/ijpo.70034. Epub 2025 Jun 17.
Previous studies suggest that in utero exposures may impact future weight gain trajectories in infancy. Leukocyte telomere length (LTL) collected at birth may be an additional variable to test in models for childhood obesity as adult studies suggest that LTL may be predictive of metabolic disease.
Using a primarily Latinx mother-child longitudinal cohort design, we assessed the relationship between newborn LTL measured via quantitative PCR and obesity at 12 months (WFA ≥ 95th percentile). Secondary outcomes included weight-for-age (WFA) Z scores at 12 months and covariates included birth anthropometrics and maternal prenatal health. Logistic and linear regression models were used to assess independent predictors for infant obesity and WFA Z scores.
We followed 302 children until 12 months including 65.89% with Latinx ethnicity and 4.97% had obesity at 12 months. Independent predictors of obesity at 12 months included higher birthweight Z scores (OR 2.24, 1.16, 5.05) and WFA Z scores at 6 months (OR 1.56, 1.19, 2.05). Longer LTL at birth and higher Apgar scores at 5 min were protective (OR 0.04, 95%CI 0.002, 0.79 and OR 0.30, 95%CI 0.13-0.72, respectively). LTL at birth was negatively associated with WFA Z scores at 12 months of age in multivariable models (Coeff = -0.58, 95%CI -1.05, -0.12).
LTL at birth may be a marker, in addition to birthweight, that can be used to assess an infant's risk for subsequent obesity. Future studies are needed to better assess and determine possible maternal exposures associated with shorter newborn LTL.
先前的研究表明,子宫内暴露可能会影响婴儿期未来的体重增加轨迹。出生时采集的白细胞端粒长度(LTL)可能是儿童肥胖模型中需要测试的另一个变量,因为成人研究表明LTL可能预测代谢疾病。
采用主要为拉丁裔母婴纵向队列设计,我们评估了通过定量PCR测量的新生儿LTL与12个月时肥胖(体重与年龄比(WFA)≥第95百分位数)之间的关系。次要结局包括12个月时的年龄别体重(WFA)Z评分,协变量包括出生时人体测量指标和母亲产前健康状况。使用逻辑回归和线性回归模型评估婴儿肥胖和WFA Z评分的独立预测因素。
我们对302名儿童进行了随访,直至12个月,其中65.89%为拉丁裔,4.97%在12个月时患有肥胖症。12个月时肥胖的独立预测因素包括较高的出生体重Z评分(比值比[OR] 2.24、1.16、5.05)和6个月时的WFA Z评分(OR 1.56、1.19、2.05)。出生时较长的LTL和5分钟时较高的阿氏评分具有保护作用(分别为OR 0.04,95%置信区间[CI] 0.002,0.79和OR 0.30,95%CI 0.13 - 0.72)。在多变量模型中,出生时的LTL与12个月龄时的WFA Z评分呈负相关(系数 = -0.58,95%CI -1.05,-0.12)。
出生时的LTL可能是除出生体重外的一个标志物,可用于评估婴儿随后发生肥胖的风险。需要进一步的研究来更好地评估和确定与新生儿LTL较短相关的可能的母亲暴露情况。