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短期口服皮质类固醇对哮喘成人饮食摄入、体重和身体成分的影响:一项随机对照试验。

Effects of short-term oral corticosteroid intake on dietary intake, body weight and body composition in adults with asthma - a randomized controlled trial.

机构信息

Centre for Asthma and Respiratory Disease, Hunter Medical Research Institute, University of Newcastle, Newcastle, NSW, Australia.

School of Medicine and Public Health, University of Newcastle, Newcastle, NSW, Australia.

出版信息

Clin Exp Allergy. 2015 May;45(5):908-919. doi: 10.1111/cea.12505.

Abstract

BACKGROUND

Oral corticosteroids (OCS) are an efficacious treatment for asthma exacerbations, yet risk of adverse effects may decrease patient adherence to therapy. In particular, changes in appetite and dietary intake, which lead to weight gain and changes in body composition, are considered undesirable.

OBJECTIVE

To determine whether 10-day OCS therapy in adults with asthma causes changes in leptin, appetite, dietary intake, body weight and body composition.

METHODS

Double-blinded, placebo-controlled randomized cross-over trial of 10 days prednisolone (50 mg) in adults with stable asthma (n = 55) (ACTRN12611000562976). Pre- and post-assessment included spirometry, body weight, body composition measured by dual-energy X-ray absorptiometry and bioelectrical impedance analysis, appetite measured using a validated visual analogue scale (VAS) and dietary intake assessed using 4-day food records. Leptin was measured as a biomarker of appetite and eosinophils as an adherence biomarker. Outcomes were analysed by generalized linear mixed models.

RESULTS

Subject adherence was confirmed by a significant decrease in blood eosinophils (× 10(9) /L) following prednisolone compared to placebo [Coef. -0.29, 95% CI: (-0.39, -0.19) P < 0.001]. There was no difference in serum leptin (ng/mL) [Coef. 0.13, 95% CI: (-3.47, 3.72) P = 0.945] or appetite measured by VAS (mm) [Coef. -4.93, 95% CI: (-13.64, 3.79) P = 0.267] following prednisolone vs. placebo. There was no difference in dietary intake (kJ/day) [Coef. 255, 95% CI: (-380, 891) P = 0.431], body weight (kg) [Coef. -0.38, 95% CI: (-0.81, 0.05) P = 0.083] or body fat (%) [Coef. -0.31, 95% CI: (-0.81, 0.20) P = 0.230]. Symptoms including sleep and gastrointestinal disturbance were reported significantly more often during prednisolone vs. placebo.

CONCLUSIONS AND CLINICAL RELEVANCE

Short-term OCS in stable asthma did not induce significant changes in appetite, dietary intake, body weight or composition, although other adverse effects may require medical management. This evidence may assist in increasing medication adherence of asthmatics prescribed OCS for exacerbations.

摘要

背景

口服皮质类固醇(OCS)是治疗哮喘加重的有效方法,但不良反应的风险可能会降低患者对治疗的依从性。特别是,食欲和饮食摄入的变化会导致体重增加和身体成分的变化,这被认为是不理想的。

目的

确定 10 天 OCS 治疗是否会导致哮喘成人的瘦素、食欲、饮食摄入、体重和身体成分发生变化。

方法

对 55 例稳定期哮喘患者(ACTRN12611000562976)进行为期 10 天的泼尼松龙(50mg)双盲、安慰剂对照随机交叉试验。预评估和后评估包括肺活量测定、体重、通过双能 X 射线吸收法和生物电阻抗分析测量的身体成分、使用经过验证的视觉模拟量表(VAS)测量的食欲以及通过 4 天食物记录评估的饮食摄入。瘦素作为食欲的生物标志物,嗜酸性粒细胞作为依从性的生物标志物进行测量。使用广义线性混合模型分析结果。

结果

通过与安慰剂相比,泼尼松龙治疗后血液嗜酸性粒细胞(× 10(9) /L)显著下降,这证实了受试者的依从性[Coef. -0.29, 95% CI: (-0.39, -0.19) P < 0.001]。与安慰剂相比,血清瘦素(ng/mL)[Coef. 0.13, 95% CI: (-3.47, 3.72) P = 0.945]或 VAS 测量的食欲[Coef. -4.93, 95% CI: (-13.64, 3.79) P = 0.267]没有差异。饮食摄入(kJ/天)[Coef. 255, 95% CI: (-380, 891) P = 0.431]、体重(kg)[Coef. -0.38, 95% CI: (-0.81, 0.05) P = 0.083]或体脂百分比[Coef. -0.31, 95% CI: (-0.81, 0.20) P = 0.230]无差异。与安慰剂相比,泼尼松龙治疗期间报告的症状(包括睡眠和胃肠道不适)明显更多。

结论和临床相关性

稳定期哮喘患者短期使用 OCS 不会引起食欲、饮食摄入、体重或身体成分的显著变化,尽管其他不良反应可能需要医学治疗。这一证据可能有助于提高哮喘患者服用 OCS 治疗加重的依从性。

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