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2
Serum 25-hydroxyvitamin D concentrations and prevalence estimates of hypovitaminosis D in the U.S. population based on assay-adjusted data.基于检测调整后数据的美国人群血清 25-羟维生素 D 浓度和维生素 D 缺乏症患病率估计。
J Nutr. 2012 Mar;142(3):498-507. doi: 10.3945/jn.111.151977. Epub 2012 Feb 8.
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Evaluation of 25-hydroxy vitamin D assay on the immunodiagnostic systems iSYS analyser.评估 iSYS 免疫诊断系统上 25-羟维生素 D 检测。
Ann Clin Biochem. 2012 Mar;49(Pt 2):159-65. doi: 10.1258/acb.2011.011018. Epub 2011 Dec 7.
4
Revised reference curves for bone mineral content and areal bone mineral density according to age and sex for black and non-black children: results of the bone mineral density in childhood study.根据年龄和性别修订的黑人和非黑人儿童骨矿物质含量和面积骨密度参考曲线:儿童骨密度研究结果。
J Clin Endocrinol Metab. 2011 Oct;96(10):3160-9. doi: 10.1210/jc.2011-1111. Epub 2011 Sep 14.
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Skeletal health of children and adolescents with inflammatory bowel disease.炎症性肠病患儿和青少年的骨骼健康。
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Bone mineral density, vitamin D, and disease activity in children newly diagnosed with inflammatory bowel disease.新诊断为炎症性肠病儿童的骨矿物质密度、维生素 D 和疾病活动度。
Dig Dis Sci. 2011 Mar;56(3):825-9. doi: 10.1007/s10620-010-1380-5. Epub 2010 Aug 20.
10
Low 25-hydroxyvitamin D levels in adolescents: race, season, adiposity, physical activity, and fitness.青少年体内 25-羟维生素 D 水平较低:种族、季节、肥胖、身体活动和健康状况。
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非裔美国克罗恩病儿童的维生素 D 状况和骨密度。

Vitamin D status and bone mineral density in African American children with Crohn disease.

机构信息

*Department of Pediatrics, Division of Gastroenterology, Hepatology, and Nutrition, Emory School of Medicine and Children's Healthcare of Atlanta †Department of Medicine, Division of Endocrinology, Metabolism, and Lipids ‡Department of Human Genetics, Emory University School of Medicine, Atlanta, GA.

出版信息

J Pediatr Gastroenterol Nutr. 2013 Nov;57(5):587-93. doi: 10.1097/MPG.0b013e31829e0b89.

DOI:10.1097/MPG.0b013e31829e0b89
PMID:23760229
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3845217/
Abstract

BACKGROUND

Vitamin D deficiency and low bone mineral density (BMD) are complications of inflammatory bowel disease. Vitamin D deficiency is more prevalent among African Americans compared with whites. There are little data comparing differences in serum 25-hydroxyvitamin D (25OHD) concentrations and BMD between African American and white children with Crohn disease (CD).

METHODS

We compared serum 25OHD concentrations of African American children with CD (n = 52) to white children with CD (n = 64) and healthy African American controls (n = 40). We also analyzed BMD using dual-energy x-ray absorptiometry results from our pediatric CD population.

RESULTS

African American children with CD had lower serum 25OHD concentrations (16.1 [95% confidence interval, CI 14.5-17.9] ng/mL) than whites with CD (22.3 [95% CI 20.2-24.6] ng/mL; P < 0.001). African Americans with CD and controls exhibited similar serum 25OHD concentration (16.1 [95% CI 14.5-17.9] vs 16.3 [95% CI 14.4-18.4] ng/mL; NS). African Americans with CD exhibited no difference in serum 25OHD concentration when controlling for seasonality, disease severity, and surgical history, although serum 25OHD concentration was significantly decreased in overweight children (body mass index ≥85%, P = 0.003). Multiple regression analysis demonstrated that obese African American girls with CD had the lowest serum 25OHD concentrations (9.6 [95% CI 6.8-13.5] ng/mL). BMD was comparable between African American and white children with CD (z score -0.4 ± 0.9 vs -0.7 ± 1.2; NS).

CONCLUSIONS

African American children with CD are more likely to have vitamin D deficiency compared with white children with CD, but have similar BMD. CD disease severity and history of surgery do not affect serum 25OHD concentrations among African American children with CD. African American children have low serum 25OHD concentrations, independent of CD, compared with white children. Future research should focus on how race affects vitamin D status and BMD in children with CD.

摘要

背景

维生素 D 缺乏和低骨密度(BMD)是炎症性肠病的并发症。与白人相比,非裔美国人中维生素 D 缺乏更为普遍。目前,比较非裔美国儿童与白人儿童克罗恩病(CD)患者血清 25-羟维生素 D(25OHD)浓度和 BMD 差异的数据较少。

方法

我们比较了 52 例非裔美国 CD 患儿(n=52)与 64 例白人 CD 患儿(n=64)和 40 例健康非裔美国对照组(n=40)的血清 25OHD 浓度。我们还利用我们儿科 CD 人群的双能 X 线吸收法(DXA)结果分析了 BMD。

结果

非裔美国 CD 患儿的血清 25OHD 浓度(16.1 [95%置信区间,CI 14.5-17.9]ng/mL)低于白人 CD 患儿(22.3 [95%CI 20.2-24.6]ng/mL;P<0.001)。非裔美国 CD 患儿和对照组的血清 25OHD 浓度相似(16.1 [95%CI 14.5-17.9]与 16.3 [95%CI 14.4-18.4]ng/mL;NS)。尽管超重儿童(体重指数≥85%,P=0.003)的血清 25OHD 浓度显著降低,但在控制季节性、疾病严重程度和手术史后,非裔美国 CD 患儿的血清 25OHD 浓度无差异。多元回归分析显示,肥胖的非裔美国 CD 女孩血清 25OHD 浓度最低(9.6 [95%CI 6.8-13.5]ng/mL)。非裔美国和白人 CD 患儿的 BMD 相当(z 评分-0.4 ± 0.9 与-0.7 ± 1.2;NS)。

结论

与白人 CD 患儿相比,非裔美国 CD 患儿更易发生维生素 D 缺乏,但 BMD 相似。CD 疾病严重程度和手术史并不影响非裔美国 CD 患儿的血清 25OHD 浓度。与白人儿童相比,非裔美国儿童无论是否患有 CD,其血清 25OHD 浓度均较低。未来的研究应重点关注种族如何影响 CD 患儿的维生素 D 状态和 BMD。