Suppr超能文献

特发性肺纤维化患者是否比其他间质性肺疾病患者更焦虑和抑郁?

Are idiopathic pulmonary fibrosis patients more anxious and depressive than patient's with other interstitial lung disease?

作者信息

Yalnız Enver, Polat Gulru, Demirci Fatma, Deniz Sami, Karadeniz Gulistan, Aydınlı Esra, Vayisoglu Gorkem, Ayrancı Aysu

机构信息

Health Science University Dr.Suat Seren Chest Diseases and Surgery Research and Training Hospital.

出版信息

Sarcoidosis Vasc Diffuse Lung Dis. 2019;36(4):294-301. doi: 10.36141/svdld.v36i4.8418. Epub 2019 May 1.

Abstract

BACKGROUND AND AIM

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive interstitial lung disease (ILD) with unknown etiology that occurs primarily in older adults with a median survival time of 2.5±3.5 years. Since there is no curative treatment for IPF, patients with IPF may have symptoms of depression and anxiety more than those of other interstitial lung diseases. There is a few studies about comparison of anxiety depression with other interstitial lung disease and IPF. In this study, we investigated whether anxiety depression in IPF was more frequent than other ILDs and its effect on quality of life.

METHODS

The study was designed as a prospective study. Age, sex, smoking status, respiratory symptoms, comorbidities, pulmonary function tests, diffusion capacity of the lungs for carbon monoxide (TLCO), SF-36, and depression/anxiety levels, radiological findings, erythrocyte sedimentation rate (ESR), CRP level, blood gas analysis, complete blood count parameters were recorded.

RESULTS

The mean age of 50 IPF and 42 non-IPF interstitial lung disease patients were 67.4±7.1 and 64.9±7.2, respectively. Compared with the non-IPF group, SF-36 total, SF-36 physical function and SF-36 physical role severity were significantly lower in the IPF group, while the GAP score was significantly higher. There was no significant difference between the two groups in HAM-Anxiety and HAM-depression for total scores. But mild anxiety was present in most of non-IPF group. No severe anxiety was observed in this group. Forty-nine of 50 patients with IPF patients had moderate-severe anxiety and the difference was statistically significant compared to non-IPF patients.

CONCLUSIONS

This is one of the first studies of anxiety and depression symptoms are also important in non IPF ILD like IPF. Patients with non-IPF ILD have similar anxiety depression with IPF patients in this study. This study led to the conclusion that anxiety depression should also be evaluated in non-IPF ILD patients.

摘要

背景与目的

特发性肺纤维化(IPF)是一种病因不明的慢性进行性间质性肺疾病(ILD),主要发生于老年人,中位生存时间为2.5±3.5年。由于IPF尚无治愈性治疗方法,与其他间质性肺疾病患者相比,IPF患者可能更易出现抑郁和焦虑症状。关于IPF与其他间质性肺疾病焦虑抑郁情况比较的研究较少。在本研究中,我们调查了IPF患者的焦虑抑郁是否比其他ILD更常见及其对生活质量的影响。

方法

本研究设计为前瞻性研究。记录年龄、性别、吸烟状况、呼吸道症状、合并症、肺功能测试、肺一氧化碳弥散量(TLCO)、SF-36、抑郁/焦虑水平、影像学检查结果、红细胞沉降率(ESR)、CRP水平、血气分析、全血细胞计数参数。

结果

50例IPF患者和42例非IPF间质性肺疾病患者的平均年龄分别为67.4±7.1岁和64.9±7.2岁。与非IPF组相比,IPF组的SF-36总分、SF-36身体功能和SF-36身体角色严重程度显著降低,而GAP评分显著升高。两组在HAM-焦虑和HAM-抑郁总分方面无显著差异。但大多数非IPF组存在轻度焦虑。该组未观察到严重焦虑。50例IPF患者中有49例存在中度至重度焦虑,与非IPF患者相比差异有统计学意义。

结论

这是首批研究之一,表明焦虑和抑郁症状在非IPF的ILD中也很重要,如同在IPF中一样。在本研究中,非IPF的ILD患者与IPF患者有相似的焦虑抑郁情况。本研究得出结论,非IPF的ILD患者也应评估焦虑抑郁情况。

相似文献

1
Are idiopathic pulmonary fibrosis patients more anxious and depressive than patient's with other interstitial lung disease?
Sarcoidosis Vasc Diffuse Lung Dis. 2019;36(4):294-301. doi: 10.36141/svdld.v36i4.8418. Epub 2019 May 1.
6
Prognosis after acute exacerbation in patients with interstitial lung disease other than idiopathic pulmonary fibrosis.
Clin Respir J. 2021 Mar;15(3):336-344. doi: 10.1111/crj.13304. Epub 2020 Dec 10.
9
ILD-specific health-related quality of life in systemic sclerosis-associated ILD compared with IPF.
BMJ Open Respir Res. 2020 Jun;7(1). doi: 10.1136/bmjresp-2020-000598.
10
Plasma Wnt7b protein in rheumatoid arthritis: Detection of interstitial lung disease.
Immunobiology. 2023 Jul;228(4):152397. doi: 10.1016/j.imbio.2023.152397. Epub 2023 May 29.

引用本文的文献

1
Mental health burden in progressive pulmonary fibrosis and idiopathic pulmonary fibrosis: Depression and anxiety.
Sarcoidosis Vasc Diffuse Lung Dis. 2025 Jun 25;42(2):16342. doi: 10.36141/svdld.v42i2.16342.
2
Mood disorder in idiopathic pulmonary fibrosis: response to pulmonary rehabilitation.
ERJ Open Res. 2023 May 22;9(3). doi: 10.1183/23120541.00585-2022. eCollection 2023 May.

本文引用的文献

1
Clinical impact of depression and anxiety in patients with idiopathic pulmonary fibrosis.
PLoS One. 2017 Sep 11;12(9):e0184300. doi: 10.1371/journal.pone.0184300. eCollection 2017.
2
Health-related quality of life in idiopathic pulmonary fibrosis: Data from the Australian IPF Registry.
Respirology. 2017 Jul;22(5):950-956. doi: 10.1111/resp.12989. Epub 2017 Feb 6.
3
Dyspnoea and comorbidity contribute to anxiety and depression in interstitial lung disease.
Respirology. 2014 Nov;19(8):1215-21. doi: 10.1111/resp.12360. Epub 2014 Aug 12.
4
Depression and anxiety predict health-related quality of life in chronic obstructive pulmonary disease: systematic review and meta-analysis.
Int J Chron Obstruct Pulmon Dis. 2014 May 20;9:501-12. doi: 10.2147/COPD.S58136. eCollection 2014.
5
The burden of idiopathic pulmonary fibrosis: an unmet public health need.
Respir Med. 2014 Jul;108(7):955-67. doi: 10.1016/j.rmed.2014.03.015. Epub 2014 Apr 13.
6
Depression in patients with idiopathic pulmonary fibrosis.
Chron Respir Dis. 2013 Aug;10(3):127-33. doi: 10.1177/1479972313493098.
7
Effect of home-based pulmonary rehabilitation in patients with idiopathic pulmonary fibrosis.
Multidiscip Respir Med. 2010 Feb 28;5(1):31-7. doi: 10.1186/2049-6958-5-1-31.
8
A multidimensional index and staging system for idiopathic pulmonary fibrosis.
Ann Intern Med. 2012 May 15;156(10):684-91. doi: 10.7326/0003-4819-156-10-201205150-00004.
9
Depression is a common and chronic comorbidity in patients with interstitial lung disease.
Respirology. 2012 Apr;17(3):525-32. doi: 10.1111/j.1440-1843.2011.02122.x.
10
An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management.
Am J Respir Crit Care Med. 2011 Mar 15;183(6):788-824. doi: 10.1164/rccm.2009-040GL.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验