Quality of life in scleroderma-related interstitial lung disease and its association with respiratory clinical parameters.

IF 1.2 Q3 RHEUMATOLOGY Journal of Scleroderma and Related Disorders Pub Date : 2025-02-24 eCollection Date: 2025-10-01 DOI:10.1177/23971983251318827
Thayalan Ponniah, Chee Kuan Wong, Choung Min Ng, Jasmin Raja
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Abstract

Objectives: Interstitial lung disease in systemic sclerosis has a significant impact in the quality of life. This prospective study was designed to determine the correlation between quality of life in systemic sclerosis-interstitial lung disease patients using patient-reported outcome measures and the lung function test parameters, with assessment done at baseline and 1 year.

Methods: In total, 63 consecutive systemic sclerosis-interstitial lung disease patients underwent lung function test, 6-minute walk distance, and quality of life-validated questionnaires (King's Brief Interstitial Lung Disease and Functional Assessment of Chronic Illness Therapy dyspnea). King's Brief Interstitial Lung Disease covers three components, namely chest, breathlessness, and psychological symptoms. The Functional Assessment of Chronic Illness Therapy dyspnea score has Part I (breathlessness symptoms) and Part II (physical limitation due to breathlessness). All assessments except for 6-minute walk distance were done both at baseline and at 12 months.

Results: Both forced vital capacity predicted percentage at baseline and 12 months had significant negative correlation with the Functional Assessment of Chronic Illness Therapy dyspnea score Part I (p values: 0.038 and <0.001, respectively). Both forced vital capacity and diffuse capacity for carbon monoxide predicted percentage at 12 months were also negatively correlated with Functional Assessment of Chronic Illness Therapy dyspnea score Part II (p values: 0.001 and 0.010, respectively). There was no significant correlation between King's Brief Interstitial Lung Disease score and the lung function parameters, at both baseline and at 1-year interval. Positive significant correlation was observed between forced vital capacity predicted percentage at baseline and 6-minute walk distance (p = 0.001).

Conclusion: Systemic sclerosis-interstitial lung disease affects quality of life, which is best assessed using the Functional Assessment of Chronic Illness Therapy dyspnea score as it correlates significantly with the lung function test parameters.

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硬皮病相关性间质性肺病患者的生活质量及其与呼吸系统临床参数的关系
目的:间质性肺疾病对系统性硬化症患者的生活质量有显著影响。这项前瞻性研究旨在通过患者报告的结果测量和肺功能测试参数确定全身性硬化-间质性肺病患者生活质量之间的相关性,并在基线和1年进行评估。方法:共63例连续的系统性硬化症-间质性肺病患者进行肺功能测试、6分钟步行距离和生活质量验证问卷(King’s Brief间质性肺病和慢性疾病治疗呼吸困难的功能评估)。金氏短暂间质性肺病包括三个组成部分,即胸部、呼吸困难和心理症状。慢性疾病治疗功能评估呼吸困难评分分为第一部分(呼吸困难症状)和第二部分(呼吸困难引起的身体限制)。除6分钟步行距离外,所有评估均在基线和12个月时进行。结果:基线和12个月时强迫肺活量预测百分比与慢性疾病治疗功能评估呼吸困难评分第一部分呈显著负相关(p值分别为0.038和0.001和0.010)。在基线和1年的时间间隔中,King's短暂间质性肺疾病评分与肺功能参数之间没有显著相关性。基线时肺活量预测百分比与6分钟步行距离呈正相关(p = 0.001)。结论:系统性硬化症-间质性肺病影响生活质量,使用慢性疾病治疗功能评估呼吸困难评分最好,因为它与肺功能测试参数显著相关。
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0.00%
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31
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