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Sex differences in physiological progression of idiopathic pulmonary fibrosis

dc.contributor.authorHan, MeiLan K.
dc.contributor.authorMurray, Susan
dc.contributor.authorFell, Charlene D.
dc.contributor.authorFlaherty, Kevin R.
dc.contributor.authorToews, Galen B.
dc.contributor.authorMyers, Jeffrey L.
dc.contributor.authorColby, Thomas V.
dc.contributor.authorTravis, William D
dc.contributor.authorKazerooni, Ella A.
dc.contributor.authorGross, Barry H.
dc.contributor.authorMartinez, Fernando J.
dc.date.accessioned2012-07-04T01:12:58Z
dc.date.available2012-07-04T01:12:58Z
dc.date.issued2008
dc.identifier.citationEuropean Respiratory Journal 2008 vol. 31 no. 6, pp. 1183 – 1188 <http://hdl.handle.net/2027.42/91966>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/91966
dc.description.abstractIn idiopathic pulmonary fibrosis, incidence is higher in males, and females may have better survival. The aim of the present study was to determine whether the rate of increase in desaturation during serial 6-min walk testing would be greater, and survival worse, for males versus females. Serial changes in the percentage of maximum desaturation area (DA) over 1 yr were estimated using mixed models in 215 patients. DA was defined as the total area above the curve created using desaturation percentage values observed during each minute of the 6-min walk test. Multivariate Cox regression assessed survival differences. Adjusting for baseline DA, 6-min walk distance, change in 6-min walk distance over time and smoking history, the percentage of maximum DA increased by an average of 2.83 and 1.37% per month for males and females, respectively. Females demonstrated better survival overall, which was more pronounced in patients who did not desaturate below 88% on ambulation at baseline and after additionally adjusting for 6-month relative changes in DA and forced vital capacity. These data suggest that differences in disease progression contribute to, but do not completely explain, better survival of females with idiopathic pulmonary fibrosis.en_US
dc.description.sponsorshipThis work was supported by National Institutes of Health grants 5P50HL56402, U10HL080371, 2K24HL04212, K12RR024987 and K23HL68713, and the Alberta Heritage Medical Foundation.en_US
dc.language.isoen_USen_US
dc.subjectDesaturationen_US
dc.subjectInterstitial Lung Diseaseen_US
dc.subject6-min Walk Testen_US
dc.subjectSurvivalen_US
dc.titleSex differences in physiological progression of idiopathic pulmonary fibrosisen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPublic Health
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/91966/1/2008 ERJ - Sex Differences in Physiologic Progression of Idiopathic Pulmonary Fibrosis.pdf
dc.identifier.sourceEuropean Respiratory Journalen_US
dc.owningcollnamePublic Health, School of (SPH)


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