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首页> 外文期刊>Journal of Korean medical science. >Vitamin D Status and Bone Mineral Density in Children with Inflammatory Bowel Disease Compared to Those with Functional Abdominal Pain
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Vitamin D Status and Bone Mineral Density in Children with Inflammatory Bowel Disease Compared to Those with Functional Abdominal Pain

机译:功能性腹痛患儿与炎症性肠病患儿的维生素D状况和骨矿物质密度

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Low vitamin D has been implicated in reduced bone mineral density (BMD) in children with inflammatory bowel disease (IBD). Our study aimed to evaluate differences in serum 25-hydroxyvitamin D (25[OH]D) and total body less head (TBLH) BMD z-scores in children with Crohn's disease (CD), ulcerative colitis (UC), and those with abdominal pain-related functional gastrointestinal disorder (AP-FGID) as the control group. We also examined the correlation between serum 25(OH)D and TBLH BMD z-score, and factors that affect each of these parameters. A total of 105 children were included and divided into 3 groups: AP-FGID (n = 45), CD (n = 43), and UC (n = 17). Among the 3 study groups, TBLH BMD z-scores were found to be significantly different (0.5 ± 0.8 in CD vs. 0.1 ± 0.8 in UC vs. ?0.1 ± 1.1 in FGID; P = 0.037), despite similar levels of serum 25(OH)D. Within each study group, correlation between serum 25(OH)D and TBLH BMD z-score was not observed. Factors found to affect the TBLH BMD z-score were sex ( P = 0.018), age ( P = 0.005) and serum hemoglobin ( P = 0.041), while factors influencing serum 25(OH)D were sex ( P = 0.018), CD with reference to AP-FGID ( P = 0.020), and serum phosphorus ( P = 0.018). Based on our results, vitamin D is a relatively small contributor to bone loss in pediatric IBD and clinicians should consider female sex, older age, and low hemoglobin as risk factors for low BMD in children with IBD. Go to: Graphical Abstract
机译:低维生素D与炎症性肠病(IBD)儿童的骨矿物质密度(BMD)降低有关。我们的研究旨在评估患有克罗恩病(CD),溃疡性结肠炎(UC)和腹部疾病的儿童的血清25-羟基维生素D(25 [OH] D)和无头颅骨(TBLH)BMD z得分的差异疼痛相关的功能性胃肠道疾病(AP-FGID)为对照组。我们还检查了血清25(OH)D和TBLH BMD z评分之间的相关性,以及影响每个参数的因素。总共包括105名儿童,分为3组:AP-FGID(n = 45),CD(n = 43)和UC(n = 17)。在3个研究组中,尽管血清25水平相似,但发现TBLH BMD z得分有显着差异(CD为0.5±0.8,UC为0.1±0.8,FGID为?0.1±1.1; P = 0.037)。 (OH)D。在每个研究组中,未观察到血清25(OH)D与TBLH BMD z评分之间的相关性。发现影响TBLH BMD z评分的因素是性别(P = 0.018),年龄(P = 0.005)和血清血红蛋白(P = 0.041),而影响血清25(OH)D的因素是性别(P = 0.018), CD参考AP-FGID(P = 0.020)和血清磷(P = 0.018)。根据我们的研究结果,维生素D对小儿IBD骨丢失的贡献相对较小,临床医生应考虑性别,年龄较大和血红蛋白低是IBD儿童BMD低的危险因素。转到:图形摘要

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