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首页> 外文期刊>Jornal de Pediatria >Prevalence of metabolic syndrome-like in the follow-up of very low birth weight preterm infants and associated factors ☆
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Prevalence of metabolic syndrome-like in the follow-up of very low birth weight preterm infants and associated factors ☆

机译:极低出生体重早产儿的随访中代谢综合征样患病率及相关因素☆

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摘要

Objective: To assess the prevalence of metabolic syndrome-like symptoms in a population of preterm infants with very low birth weight (1500 g) at 2 years of corrected age and identify the occurrence of associated risk factors. Methods: Cross-sectional study during a five-year period, including preterm infants born with very low birth weight evaluated at 2 years of corrected age. Metabolic syndrome-like symptoms was defined by the presence of three or more of these criteria: abdominal circumference ≥ 90th percentile, fasting blood glucose ≥ 100 mg/dL, triglycerides ≥ 110 mg/dL, HDL cholesterol ≤ 40 mg/dL, and blood pressure ≥ 90th percentile. Results: A total of 214 preterm infants with birth weight 1500 g were evaluated. The prevalence of metabolic syndrome-like symptoms at 2 years of corrected age was 15.1%. Arterial hypertension was present in 57.5%, HDL ≤ 40 mg/dL in 29.2%, hypertriglyceridemia in 22.6%, and abdominal circumference above the 90th percentile in 18.8%. Only 3.7% had hyperglycemia. The presence of periventricular leukomalacia was an independent risk factor for arterial hypertension at this age (OR 2.34, 95% CI: 0.079–0.69, p = 0.008). Overweight and obesity at 2 years of corrected age were independently associated with metabolic syndrome-like symptoms (OR 2.75, 95% CI: 1.19–6.36, p = 0.018). Conclusion: Metabolic syndrome-like symptoms can be observed in very low birth weight preterm infants as early as 2 years of corrected age. Overweight and early-onset obesity are significant risk factors for metabolic syndrome-like symptoms, which deserves appropriate intervention for this high-risk population.
机译:目的:评估在校正年龄的2岁时出生体重非常低(<1500 g)的早产儿中代谢综合征样症状的发生率,并确定相关危险因素的发生。方法:为期五年的横断面研究,包括在校正年龄的2岁时评估的出生时极低体重的早产儿。代谢综合征样症状由以下三个或三个以上标准定义:腹围≥90%,空腹血糖≥100 mg / dL,甘油三酸酯≥110 mg / dL,HDL胆固醇≤40 mg / dL和血液压力≥90%。结果:评估了214名出生体重<1500 g的早产儿。在校正年龄的2岁时,代谢综合征样症状的患病率为15.1%。动脉高血压的发生率为57.5%,HDL≤40 mg / dL的发生率为29.2%,高甘油三酯血症的发生率为22.6%,腹围高于90%的患者为18.8%。只有3.7%的人有高血糖症。脑室周围白细胞软化的存在是该年龄段动脉高血压的独立危险因素(OR 2.34,95%CI:0.079-0.69,p = 0.008)。在校正年龄的2岁时超重和肥胖与代谢综合征样症状独立相关(OR 2.75,95%CI:1.16-6.36,p = 0.018)。结论:早在校正年龄的2岁就可以在极低出生体重的早产儿中观察到类似代谢综合征的症状。超重和早发型肥胖是代谢综合症样症状的重要危险因素,对此高危人群应采取适当的干预措施。

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