Cherniack R M, Colby T V, Flint A, Thurlbeck W M, Waldron J A, Ackerson L, Schwarz M I, King T E
Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, University of Colorado, Denver 80206.
Am J Respir Crit Care Med. 1995 Apr;151(4):1180-8. doi: 10.1164/ajrccm/151.4.1180.
The early stage of idiopathic pulmonary fibrosis (IPF) is thought to involve a smaller number of alveoli and to be characterized predominantly by cellularity and minimal fibrosis, whereas advanced disease involves a large number of alveoli and is characterized predominantly by fibrosis with minimal cellularity. In addition, correlative studies have indicated that prognosis and response to therapy is determined in part by the extent of fibrosis and cellularity. This study was undertaken to determine whether pulmonary function assessment would help distinguish between the cellular and fibrotic phases of this disorder, as determined by a semiquantitative pathology scoring system that comprised four factor scores: fibrosis, cellularity, granulation/connective tissue, and desquamation. Ninety-six untreated patients with biopsy-confirmed IPF (27 never smokers, 32 current smokers, and 37 ex-smokers) were evaluated. In the group as a whole, there was no significant relationship between the fibrosis or the connective/granulation tissue factor scores and any of the physiologic parameters. The DLCO correlated with the "desquamation" and the total pathology scores, whereas the TLC and FVC correlated with the cellularity factor score. In the current smokers, the coefficient of elastic retraction, DLCO/VA, and FEV1/FVC ratio were significantly lower than in never smokers and ex-smokers, and TLC and FVC were higher than in never smokers. Also, the mean cellularity and granulation/connective tissue factor scores were significantly lower, and the desquamation factor score was significantly higher than those in never smokers and ex-smokers. Both age and smoking status were significant for the cellularity factor score, whereas for the connective/granulation tissue factor score, age was not significant but smoking status was.(ABSTRACT TRUNCATED AT 250 WORDS)
特发性肺纤维化(IPF)的早期阶段被认为涉及较少数量的肺泡,主要特征为细胞增多和极少的纤维化,而晚期疾病涉及大量肺泡,主要特征为纤维化且细胞极少。此外,相关性研究表明,预后和对治疗的反应部分取决于纤维化和细胞增多的程度。本研究旨在确定肺功能评估是否有助于区分该疾病的细胞期和纤维化期,这是通过一个半定量病理评分系统确定的,该系统包括四个因子评分:纤维化、细胞增多、肉芽组织/结缔组织和脱屑。对96例经活检确诊为IPF的未治疗患者(27例从不吸烟者、32例当前吸烟者和37例既往吸烟者)进行了评估。在整个组中,纤维化或结缔组织/肉芽组织因子评分与任何生理参数之间均无显著关系。一氧化碳弥散量(DLCO)与“脱屑”及总病理评分相关,而肺总量(TLC)和用力肺活量(FVC)与细胞增多因子评分相关。在当前吸烟者中,弹性回缩系数、DLCO/肺泡容积(VA)和第一秒用力呼气容积/用力肺活量(FEV1/FVC)比值显著低于从不吸烟者和既往吸烟者,且TLC和FVC高于从不吸烟者。此外,平均细胞增多和肉芽组织/结缔组织因子评分显著低于从不吸烟者和既往吸烟者,脱屑因子评分显著高于从不吸烟者和既往吸烟者。年龄和吸烟状态对细胞增多因子评分均有显著影响,而对于结缔组织/肉芽组织因子评分,年龄无显著影响,但吸烟状态有显著影响。(摘要截短于250字)