Body mass index and mortality in patients with idiopathic pulmonary fibrosis

被引:129
作者
Alakhras, Mazen
Decker, Paul A.
Nadrous, Hassan F.
Collazo-Clavell, Maria
Ryu, Jay H.
机构
[1] Mayo Clin, Div Pulm & Crit Care Med, Rochester, MN 55905 USA
[2] Mayo Clin, Div Biostat, Rochester, MN 55905 USA
[3] Mayo Clin, Div Endocrinol Diabet Metab & Nutr, Rochester, MN 55905 USA
关键词
body mass index; interstitial lung disease; mortality; nutrition; prognosis; pulmonary fibrosis;
D O I
10.1378/chest.06-2784
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: To examine the relationship between body mass index (BMI) and mortality in patients with idiopathic pulmonary fibrosis (IPF). Methods: We studied a cohort of. patients with IPF who were seen at the Mayo Clinic Rochester from 1994 through 1996. These patients met the current consensus definition of IPF. We excluded patients who had received prior treatment for IPF, had no follow-up data, or had no pulmonary function results available at the index visit. Results: Of the 197 patients fulfilling the inclusion criteria, the mean ( +/- SD) age was 71.4 +/- 8.9 years, 137 patients (70%) were men, and the mean BMI was 28.2 +/- 4.6. These patients were categorized by BMI into the following three groups: < 25; 25 to 30; and >= 30. There were 46 patients (23%) with a BMI of < 25 who had a median survival time of 3.6 years (1-year survival rate, 76% [95% confidence interval (CI), 65 to 90%]; 3-year survival rate, 54% [95% CI, 41 to 70%]). The second group consisted of 85 patients (43%) with a BMI between 25 and 30 who had a median survival time of 3.8 years (1-year survival rate, 84% [95% CI, 76 to 92%]; 3-year survival rate, 58% [95% CI, 48 to 70%]). The final group consisted of 66 patients (34%) with a BMI of >= 30 and who had a median survival time of 5.8 years (1-year survival rate, 91% [95% CI, 84 to 98%]; 3-year survival rate, 69% [95% CI, 58 to 81%]). Using a proportional hazards regression model, survival was significantly associated with BMI (hazard ratio, 0.93 for each I-U increase in BMI; 95% CI, 0.89 to 0.97; p = 0.002) with increased BMI being associated with better survival. Conclusion: Higher BMI was associated with better survival in patients with IPF.
引用
收藏
页码:1448 / 1453
页数:6
相关论文
共 41 条
[1]  
[Anonymous], 2000, AM J RESP CRIT CARE, V161, P646, DOI DOI 10.1164/AJRCCM.161.2.ATS3-00
[2]  
Ask Kjetil, 2006, Proc Am Thorac Soc, V3, P389, DOI 10.1513/pats.200602-021TK
[3]   Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis [J].
Bjoraker, JA ;
Ryu, JH ;
Edwin, MK ;
Myers, JL ;
Tazelaar, HD ;
Schroeder, DR ;
Offord, KP .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (01) :199-203
[4]   C-reactive protein and body mass index predict outcome in end-stage respiratory failure [J].
Cano, NJM ;
Pichard, C ;
Roth, H ;
Court-Fortuné, I ;
Cynober, L ;
Gérard-Boncompain, M ;
Cuvelier, A ;
Laaban, JP ;
Melchior, JC ;
Raphaël, JC ;
Pison, CM .
CHEST, 2004, 126 (02) :540-546
[5]   The body-mass index, airflow obstruction, dyspnea, and exercise capacity index in chronic obstructive pulmonary disease [J].
Celli, BR ;
Cote, CG ;
Marin, JM ;
Casanova, C ;
de Oca, MM ;
Mendez, RA ;
Pinto Plata, V ;
Cabral, HJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (10) :1005-1012
[6]   Predictors of survival in patients receiving domiciliary oxygen therapy or mechanical ventilation - A 10-year analysis of ANTADIR Observatory [J].
Chailleux, E ;
Fauroux, B ;
Binet, F ;
Dautzenberg, B ;
Polu, JM .
CHEST, 1996, 109 (03) :741-749
[7]   Prognostic value of nutritional depletion in patients with COPD treated by long-term oxygen therapy - Data from the ANTADIR Observatory [J].
Chailleux, E ;
Laaban, JP ;
Veale, D .
CHEST, 2003, 123 (05) :1460-1466
[8]   Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosis [J].
Collard, HR ;
King, TE ;
Bartelson, BB ;
Vourlekis, JS ;
Schwarz, MI ;
Brown, KK .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 168 (05) :538-542
[9]  
COX DR, 1972, J R STAT SOC B, V34, P187
[10]   Treatment of idiopathic pulmonary fibrosis [J].
Daniels, Craig E. ;
Ryu, Jay H. .
SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 27 (06) :668-676