Vitamin D Level, Weight, Height, and BMI Among Children with Cystic Fibrosis: A Retrospective Study

M. Ahmadi, Mohammadreza Mirkarimi, Shabnam Khanifar, H. Javaherizadeh, Mohsen Ali Samir
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Abstract

Background: Cystic fibrosis (CF) stands as the most common chronic multisystem and fatal inherited disease. Objectives: The present study aimed to assess the clinical presentation and laboratory findings in children with CF. Methods: This retrospective cross-sectional study reviewed the records of CF patients over a 2-year period beginning in 2018. The diagnosis of CF was confirmed based on clinical manifestations, sweat chloride tests, or genetic studies. Children aged ≥ 2 years were included; nevertheless, patients without sweat chloride tests or genetic studies were excluded. This study recorded demographic features, gastrointestinal manifestations, vitamin D levels, and the number of hospital admissions. A pediatric gastroenterologist conducted fecal elastase and stool fat analyses to evaluate pancreatic insufficiency. Vitamin D levels < 30 ng/mL were considered vitamin D insufficiency; however, levels < 20 ng/mL indicated a vitamin D deficiency. A P-value < 0.05 was considered statistically significant. Results: This study included 59 children (37 male and 22 female) in the study. Low weight, height, and body mass index (BMI) percentiles (< 5) were most frequently observed. Approximately 86.4% of the patients had consanguineous parents, and 40.7% had affected siblings. Failure to thrive (FTT) (49.2%) and recurrent respiratory infections (45.8%) were the most common clinical presentations. A majority (57.7%) of the patients were diagnosed before the age of 1 year. The mean number of admissions in the past 2 years was 3, and 58% of the cases reported gastrointestinal symptoms. A significant correlation was observed between vitamin D levels and the number of hospital admissions (Pearson coefficient = 0.298, P = 0.042). Conclusions: In this study, there was a high prevalence of vitamin D insufficiency and FTT in children with CF. Additionally, there was a significant correlation between vitamin D levels and the number of hospital admissions over a 2-year period.
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囊性纤维化儿童的维生素 D 水平、体重、身高和体重指数:一项回顾性研究
背景:囊性纤维化(CF)是最常见的慢性多系统致命性遗传疾病。研究目的本研究旨在评估囊性纤维化患儿的临床表现和实验室检查结果。方法:这是一项回顾性横断面研究:这项回顾性横断面研究回顾了自 2018 年开始的两年内 CF 患者的病历。CF的诊断是根据临床表现、汗液氯化物检测或基因研究确诊的。年龄≥2岁的儿童被纳入研究范围;然而,未进行汗液氯化物检测或基因研究的患者被排除在外。本研究记录了人口统计学特征、胃肠道表现、维生素 D 水平和入院次数。一名儿科胃肠病专家进行了粪便弹性蛋白酶和粪便脂肪分析,以评估胰腺功能不全。维生素D水平<30纳克/毫升被认为是维生素D不足;然而,维生素D水平<20纳克/毫升则表示维生素D缺乏。P 值小于 0.05 视为具有统计学意义。研究结果本研究共纳入 59 名儿童(37 名男性和 22 名女性)。体重、身高和体重指数(BMI)百分位数(小于 5)偏低的情况最为常见。约 86.4% 的患者父母是近亲,40.7% 的患者有受影响的兄弟姐妹。发育不良(49.2%)和反复呼吸道感染(45.8%)是最常见的临床表现。大多数患者(57.7%)在一岁前被确诊。过去两年入院的平均次数为 3 次,58% 的病例报告了胃肠道症状。维生素 D 水平与入院次数之间存在明显相关性(皮尔逊系数 = 0.298,P = 0.042)。结论在这项研究中,CF 患儿维生素 D 不足和 FTT 的发病率很高。此外,维生素 D 水平与两年内入院次数之间存在显著相关性。
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