Yukiko Kunitomo, Han Woo, Aparna Balasubramanian, Ashraf Fawzy, Cheng Ting Lin, Sarath Raju, Daniel C Belz, Meredith C McCormack, Kirsten Koehler, Nadia N Hansel, Nirupama Putcha
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The objective of this study was to evaluate the association between longitudinal anemia status and COPD outcomes, accounting for comorbid cardiovascular disease.</p><p><strong>Methods: </strong>Serial hemoglobin measures and clinical outcomes were obtained in former smokers with moderate to severe COPD from two clinical studies over a 6-to-9-month period. In the first analysis, the association between repeated measures of time-varying anemia status and outcomes was assessed by generalized estimating equations adjusted for covariates including cardiovascular disease. In the second analysis, each participant's anemia risk profile during the study period was characterized as high versus low anemia risk-growth rate. Mean differences in the progression of COPD outcomes over time between the two groups were assessed using a generalized linear mixed model. Effect modification by baseline coronary artery calcium (CAC) burden was explored.</p><p><strong>Results: </strong>There were 159 individuals with mean age of 66.5 years (± 8.3) and mean FEV<sub>1</sub>% predicted of 51.4% (± 17.0), of which 41% were ever-anemic during the study period. Repeated measures of anemia status were associated with higher St. George's Respiratory Questionnaire (SGRQ) scores (β 2.5, 95% CI: 0.1,4.8, p = 0.04), lower 6-minute walk distance (6MWD) (β -38.6, 95% CI: -67.7,-7.4, p = 0.02), and higher rate of moderate-to-severe exacerbations over the prospective follow-up period (IRR 1.8, 95% CI: 1.1,2.8, p = 0.02). There was effect modification by CAC burden such that with higher burden the mean difference in COPD outcome by anemia status was greater for a subset of symptom scores. Participants with profiles of increasing anemia risk had higher estimated rates of decline in the FEV<sub>1</sub>% predicted and 6MWD and increase in SGRQ scores compared to those with stable or decreasing anemia risk.</p><p><strong>Conclusions: </strong>Longitudinal anemia status trends may be predictive of COPD disease trajectory. 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However, the significance of longitudinal anemia status and variation in anemia status trends over time in COPD are not known. Furthermore, individuals with COPD and smoking history often have multiple comorbidities, in particular cardiovascular disease. The objective of this study was to evaluate the association between longitudinal anemia status and COPD outcomes, accounting for comorbid cardiovascular disease.</p><p><strong>Methods: </strong>Serial hemoglobin measures and clinical outcomes were obtained in former smokers with moderate to severe COPD from two clinical studies over a 6-to-9-month period. In the first analysis, the association between repeated measures of time-varying anemia status and outcomes was assessed by generalized estimating equations adjusted for covariates including cardiovascular disease. In the second analysis, each participant's anemia risk profile during the study period was characterized as high versus low anemia risk-growth rate. Mean differences in the progression of COPD outcomes over time between the two groups were assessed using a generalized linear mixed model. Effect modification by baseline coronary artery calcium (CAC) burden was explored.</p><p><strong>Results: </strong>There were 159 individuals with mean age of 66.5 years (± 8.3) and mean FEV<sub>1</sub>% predicted of 51.4% (± 17.0), of which 41% were ever-anemic during the study period. Repeated measures of anemia status were associated with higher St. George's Respiratory Questionnaire (SGRQ) scores (β 2.5, 95% CI: 0.1,4.8, p = 0.04), lower 6-minute walk distance (6MWD) (β -38.6, 95% CI: -67.7,-7.4, p = 0.02), and higher rate of moderate-to-severe exacerbations over the prospective follow-up period (IRR 1.8, 95% CI: 1.1,2.8, p = 0.02). There was effect modification by CAC burden such that with higher burden the mean difference in COPD outcome by anemia status was greater for a subset of symptom scores. 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引用次数: 0
摘要
背景:贫血是COPD的常见合并症,与发病率增加有关。然而,慢性阻塞性肺病纵向贫血状态和贫血状态随时间变化趋势的意义尚不清楚。此外,患有慢性阻塞性肺病和吸烟史的个体通常有多种合并症,特别是心血管疾病。本研究的目的是评估纵向贫血状态与COPD结局之间的关系,并考虑合并症心血管疾病。方法:从两项6- 9个月的临床研究中获得了中度至重度COPD前吸烟者的一系列血红蛋白测量和临床结果。在第一个分析中,反复测量时变贫血状态和结果之间的关联通过调整协变量(包括心血管疾病)的广义估计方程进行评估。在第二个分析中,每个参与者在研究期间的贫血风险概况被描述为高与低贫血风险增长率。使用广义线性混合模型评估两组间COPD结局进展的平均差异。探讨基线冠状动脉钙负荷对疗效的影响。结果:159例患者平均年龄66.5岁(±8.3岁),平均FEV1%预测值为51.4%(±17.0),其中41%在研究期间出现过贫血。重复测量贫血状态与较高的圣乔治呼吸问卷(SGRQ)评分(β - 2.5, 95% CI: 0.1,4.8, p = 0.04),较低的6分钟步行距离(6MWD) (β -38.6, 95% CI: -67.7,-7.4, p = 0.02)以及在预期随访期间较高的中重度恶化率(IRR 1.8, 95% CI: 1.1,2.8, p = 0.02)相关。CAC负担改变了效果,在症状评分的一个子集中,加重的CAC负担导致贫血状态导致COPD结局的平均差异更大。与贫血风险稳定或降低的参与者相比,贫血风险增加的参与者在FEV1%预测和6MWD的估计下降率和SGRQ评分的增加率更高。结论:纵向贫血状态趋势可预测COPD疾病发展轨迹。通过重复测量分析,贫血状态与COPD发病率相关,在高CAC负担的情况下可能存在更强的相关性。
Longitudinal anemia status and risk for adverse outcomes in former smokers with COPD.
Background: Anemia is a prevalent comorbidity in COPD associated with increased morbidity. However, the significance of longitudinal anemia status and variation in anemia status trends over time in COPD are not known. Furthermore, individuals with COPD and smoking history often have multiple comorbidities, in particular cardiovascular disease. The objective of this study was to evaluate the association between longitudinal anemia status and COPD outcomes, accounting for comorbid cardiovascular disease.
Methods: Serial hemoglobin measures and clinical outcomes were obtained in former smokers with moderate to severe COPD from two clinical studies over a 6-to-9-month period. In the first analysis, the association between repeated measures of time-varying anemia status and outcomes was assessed by generalized estimating equations adjusted for covariates including cardiovascular disease. In the second analysis, each participant's anemia risk profile during the study period was characterized as high versus low anemia risk-growth rate. Mean differences in the progression of COPD outcomes over time between the two groups were assessed using a generalized linear mixed model. Effect modification by baseline coronary artery calcium (CAC) burden was explored.
Results: There were 159 individuals with mean age of 66.5 years (± 8.3) and mean FEV1% predicted of 51.4% (± 17.0), of which 41% were ever-anemic during the study period. Repeated measures of anemia status were associated with higher St. George's Respiratory Questionnaire (SGRQ) scores (β 2.5, 95% CI: 0.1,4.8, p = 0.04), lower 6-minute walk distance (6MWD) (β -38.6, 95% CI: -67.7,-7.4, p = 0.02), and higher rate of moderate-to-severe exacerbations over the prospective follow-up period (IRR 1.8, 95% CI: 1.1,2.8, p = 0.02). There was effect modification by CAC burden such that with higher burden the mean difference in COPD outcome by anemia status was greater for a subset of symptom scores. Participants with profiles of increasing anemia risk had higher estimated rates of decline in the FEV1% predicted and 6MWD and increase in SGRQ scores compared to those with stable or decreasing anemia risk.
Conclusions: Longitudinal anemia status trends may be predictive of COPD disease trajectory. Anemia status by repeated measures analysis is associated with COPD morbidity with potentially stronger associations in the setting of high CAC burden.
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.