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苏格兰儿科癌症患者的5-羟维生素D浓度:一项前瞻性队列研究。

5-Hydroxyvitamin D concentration in paediatric cancer patients from Scotland: a prospective cohort study.

作者信息

Iniesta Raquel Revuelta, Paciarotti Ilenia, Davidson Isobel, McKenzie Jane M, Brand Celia, Chin Richard F M, Brougham Mark F H, Wilson David C

机构信息

1Dietetics, Nutrition and Biological Health Sciences,Queen Margaret University,Edinburgh,EH21 6UU,UK.

3Department of Paediatric Neuroscience,Royal Hospital for Sick Children,Edinburgh,EH9 1LF,UK.

出版信息

Br J Nutr. 2016 Dec;116(11):1926-1934. doi: 10.1017/S0007114516004074. Epub 2016 Dec 15.

Abstract

Children with cancer are potentially at a high risk of plasma 25-hydroxyvitamin D (25(OH)D) inadequacy, and despite UK vitamin D supplementation guidelines their implementation remains inconsistent. Thus, we aimed to investigate 25(OH)D concentration and factors contributing to 25(OH)D inadequacy in paediatric cancer patients. A prospective cohort study of Scottish children aged 75 nmol/l). In all, eighty-two patients (median age 3·9, interquartile ranges (IQR) 1·9-8·8; 56 % males) and thirty-five controls (median age 6·2, IQR 4·8-9·1; 49 % males) were recruited. 25(OH)D inadequacy was highly prevalent in the controls (63 %; 22/35) and in the patients (64 %; 42/65) at both baseline and during treatment (33-50 %). Non-supplemented children had the highest prevalence of 25(OH)D inadequacy at every stage with 25(OH)D median ranging from 32·0 (IQR 21·0-46·5) to 45·0 (28·0-64·5) nmol/l. Older age at baseline (R -0·46; P<0·001), overnutrition (BMI≥85th centile) at 3 months (P=0·005; relative risk=3·1) and not being supplemented at 6 months (P=0·04; relative risk=4·3) may have contributed to lower plasma 25(OH)D. Paediatric cancer patients are not at a higher risk of 25(OH)D inadequacy than healthy children at diagnosis; however, prevalence of 25(OH)D inadequacy is still high and non-supplemented children have a higher risk. Appropriate monitoring and therapeutic supplementation should be implemented.

摘要

患癌儿童血浆25-羟维生素D(25(OH)D)不足的风险可能很高,尽管英国有维生素D补充指南,但这些指南的实施情况仍不一致。因此,我们旨在调查儿科癌症患者的25(OH)D浓度以及导致25(OH)D不足的因素。对75名年龄在1至18岁之间的苏格兰儿童进行了一项前瞻性队列研究,这些儿童被诊断患有癌症或作为健康对照。排除标准包括维生素D缺乏或过量的既往史、严重的急性疾病、正在进行的维生素D补充以及其他可能影响维生素D状态的疾病。通过酶联免疫吸附测定法(ELISA)测量血清25(OH)D浓度。25(OH)D不足定义为血清浓度低于50 nmol/l,严重不足定义为低于25 nmol/l,充足定义为≥75 nmol/l。总共招募了82名患者(中位年龄3.9岁,四分位间距(IQR)1.9 - 8.8岁;56%为男性)和35名对照(中位年龄6.2岁,IQR 4.8 - 9.1岁;49%为男性)。在基线和治疗期间,对照组(63%;22/35)和患者组(64%;42/65)中25(OH)D不足的情况都非常普遍(33 - 50%)。未补充维生素D的儿童在每个阶段25(OH)D不足的患病率最高,25(OH)D中位数范围为32.0(IQR 21.0 - 46.5)至45.0(28.0 - 64.5)nmol/l。基线时年龄较大(R -0.46;P<0.001)、3个月时营养过剩(BMI≥第85百分位数)(P = 0.005;相对风险 = )和6个月时未补充维生素D(P = 0.04;相对风险 = 4.3)可能导致血浆25(OH)D水平降低。在诊断时,儿科癌症患者25(OH)D不足的风险并不高于健康儿童;然而,25(OH)D不足的患病率仍然很高,未补充维生素D的儿童风险更高。应实施适当的监测和治疗性补充。 (注:原文中“relative risk=3·1”处表述不完整,翻译时保留了原文格式)

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