The longitudinal impact of low-dose morphine on diurnal cortisol profiles in people with chronic breathlessness and chronic obstructive pulmonary disease (COPD): an exploratory study.

IF 5.8 2区 医学 Q1 Medicine
Diana H Ferreira, Richella Ryan, Nina Smyth, Angela Clow, David C Currow
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引用次数: 0

Abstract

Introduction: Stress activates the hypothalamic-pituitary-adrenal (HPA) axis of which cortisol is an end product. 'Allostatic load' is where systems including the HPA axis are exposed to high, cumulative, physiologic burdens (such as chronic breathlessness) leading to flatter diurnal cortisol slopes and poorer health outcomes. The aim of this hypothesis-generating study explored longitudinal changes in cortisol secretion and any associated changes in breathlessness after introducing regular, low dose morphine or placebo.

Methods: This was an optional, hypothesis-generating sub-study embedded in a multi-site, randomised, double-blind, placebo-controlled trial (RCT) of regular, low-dose morphine for chronic breathlessness and chronic obstructive pulmonary disease. In a blinded dose-increment algorithm by week three, doses were 0 mg-32 mg. Participants in the RCT could elect to continue in a six-month blinded extension. This sub-study excluded people who used non-inhaled corticosteroids in the previous month or were on subcutaneous insulin. Participants collected saliva for cortisol assays for two days at baseline, and ends of weeks 1, 3 and 12 at 3,6 and 12 h after waking, generating sufficient data to calculate diurnal cortisol slopes and areas under the curve (AUC). Samples were analysed using ELISA. Correlations between diurnal cortisol profiles (slope and AUC) and a range of measures were explored.

Results: Twenty mostly female former smokers were in this sub-study. At baseline and the end of week 1, one-way ANOVA between-group analyses showed no significant differences in the log-transformed cortisol slope or ln-AUC. There was a strong correlation between the age-adjusted Charlson Comorbidity Index (CCI) and ln-AUC (r=-0.70, p < 0.001) and moderate correlation with age (r=-0.43, p = 0.06). In the blinded extension study, there was a self-selecting blinded group (n = 7) all on active medication. Global impression of change (GIC) was highly correlated with the diurnal cortisol slope (rs = 0.98, p = 0.01), and with decrease in average breathlessness (r = 0.89, p = 0.04).

Discussion: This hypothesis-generating study did not show a relationship between the diurnal cortisol profile and morphine in people with chronic breathlessness and COPD. For the sub-group still on study at 12weeks, the cortisol curves became steeper as average breathlessness decreased and as global impression of change (GIC) improved, suggesting that reducing breathlessness may potentially positively impact the HPA axis in a sub-group of people.

Trial registration: Registration Number NCT02720822 date registered 28/03/2016.

低剂量吗啡对慢性呼吸困难和慢性阻塞性肺疾病(COPD)患者日皮质醇谱的纵向影响:一项探索性研究
简介:压力激活下丘脑-垂体-肾上腺(HPA)轴,皮质醇是其最终产物。“适应负荷”是指包括下丘脑轴在内的系统暴露于高的、累积的生理负荷(如慢性呼吸困难)下,导致皮质醇的日斜率变平,健康状况变差。这项产生假设的研究的目的是探索皮质醇分泌的纵向变化,以及在引入常规、低剂量吗啡或安慰剂后呼吸困难的任何相关变化。方法:这是一项可选的、产生假设的子研究,嵌入在一项多地点、随机、双盲、安慰剂对照试验(RCT)中,研究常规、低剂量吗啡治疗慢性呼吸困难和慢性阻塞性肺疾病。在第三周的盲法剂量递增算法中,剂量为0 mg-32 mg。随机对照试验的参与者可以选择继续进行6个月的盲法延长试验。这项亚研究排除了在前一个月使用非吸入性皮质类固醇或皮下注射胰岛素的人。参与者在基线时收集唾液进行皮质醇测定,并在第1、3和12周结束时在醒来后的3、6和12小时收集唾液进行皮质醇测定,产生足够的数据来计算日皮质醇斜率和曲线下面积(AUC)。采用ELISA法对样品进行分析。探讨了皮质醇日变化曲线(斜率和AUC)与一系列测量指标之间的相关性。结果:本亚研究共纳入20例戒烟者,多数为女性。在基线和第1周结束时,组间单因素方差分析显示,对数转换的皮质醇斜率或ln-AUC没有显著差异。年龄校正的Charlson合并症指数(CCI)和ln-AUC之间有很强的相关性(r=-0.70, p)。讨论:这项产生假设的研究没有显示慢性呼吸困难和COPD患者的日皮质醇水平和吗啡之间的关系。对于12周仍在研究的亚组,皮质醇曲线随着平均呼吸困难的减少和整体印象变化(GIC)的改善而变得陡峭,这表明减少呼吸困难可能对亚组人群的下丘脑轴有潜在的积极影响。试验注册:注册号NCT02720822,注册日期28/03/2016。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Respiratory Research
Respiratory Research RESPIRATORY SYSTEM-
CiteScore
9.70
自引率
1.70%
发文量
314
审稿时长
4-8 weeks
期刊介绍: Respiratory Research publishes high-quality clinical and basic research, review and commentary articles on all aspects of respiratory medicine and related diseases. As the leading fully open access journal in the field, Respiratory Research provides an essential resource for pulmonologists, allergists, immunologists and other physicians, researchers, healthcare workers and medical students with worldwide dissemination of articles resulting in high visibility and generating international discussion. Topics of specific interest include asthma, chronic obstructive pulmonary disease, cystic fibrosis, genetics, infectious diseases, interstitial lung diseases, lung development, lung tumors, occupational and environmental factors, pulmonary circulation, pulmonary pharmacology and therapeutics, respiratory immunology, respiratory physiology, and sleep-related respiratory problems.
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