Longitudinal Phenotypes and Mortality in Preserved Ratio Impaired Spirometry in the COPDGene Study

Increasing awareness of the prevalence and significance of Preserved Ratio Impaired Spirometry (PRISm), alternatively known as restrictive or Global Initiative for Chronic Obstructive Lung Disease (GOLD)-unclassified spirometry, has expanded the body of knowledge on cross-sectional risk factors. How...

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Published inAmerican journal of respiratory and critical care medicine Vol. 198; no. 11; pp. 1397 - 1405
Main Authors Wan, Emily S., Fortis, Spyridon, Regan, Elizabeth A., Hokanson, John, Han, MeiLan K., Casaburi, Richard, Make, Barry J., Crapo, James D., DeMeo, Dawn L., Silverman, Edwin K., Beaty, Terri, Begum, Ferdouse, Castaldi, Peter J., Cho, Michael, Boueiz, Adel R., Foreman, Marilyn G., Halper-Stromberg, Eitan, Hayden, Lystra P., Hersh, Craig P., Hetmanski, Jacqueline, Hobbs, Brian D., Hokanson, John E., Laird, Nan, Lange, Christoph, Lutz, Sharon M., McDonald, Merry-Lynn, Parker, Margaret M., Qiao, Dandi, Won, Sungho, Sakornsakolpat, Phuwanat, Prokopenko, Dmitry, Al Qaisi, Mustafa, Coxson, Harvey O., Gray, Teresa, Hoffman, Eric A., Humphries, Stephen, Jacobson, Francine L., Judy, Philip F., Kazerooni, Ella A., Kluiber, Alex, Lynch, David A., Newell, John D., Ross, James C., San Jose Estepar, Raul, Schroeder, Joyce, Sieren, Jered, Stinson, Douglas, Stoel, Berend C., Tschirren, Juerg, Van Beek, Edwin, van Ginneken, Bram, van Rikxoort, Eva, Washko, George, Wilson, Carla G., Jensen, Robert, Everett, Douglas, Crooks, Jim, Moore, Camille, Strand, Matt, Hughes, John, Kinney, Gregory, Pratte, Katherine, Young, Kendra A., Bhatt, Surya, Bon, Jessica, Make, Barry, Martinez, Carlos, Murray, Susan, Regan, Elizabeth, Soler, Xavier, Bowler, Russell P., Kechris, Katerina, Banaei-Kashani, Farnoush, Curtis, Jeffrey L., Martinez, Carlos H., Pernicano, Perry G., Hanania, Nicola, Alapat, Philip, Atik, Mustafa, Bandi, Venkata, Boriek, Aladin, Guntupalli, Kalpatha, Guy, Elizabeth, Nachiappan, Arun, Parulekar, Amit, Hersh, Craig, Barr, R. Graham, Austin, John, D’Souza, Belinda, Pearson, Gregory D. N., Rozenshtein, Anna, Thomashow, Byron, MacIntyre, Neil
Format Journal Article
LanguageEnglish
Published United States American Thoracic Society 01.12.2018
Subjects
Online AccessGet full text
ISSN1073-449X
1535-4970
1535-4970
DOI10.1164/rccm.201804-0663OC

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Abstract Increasing awareness of the prevalence and significance of Preserved Ratio Impaired Spirometry (PRISm), alternatively known as restrictive or Global Initiative for Chronic Obstructive Lung Disease (GOLD)-unclassified spirometry, has expanded the body of knowledge on cross-sectional risk factors. However, longitudinal studies of PRISm remain limited. To examine longitudinal patterns of change in lung function, radiographic characteristics, and mortality of current and former smokers with PRISm. Current and former smokers, aged 45 to 80 years, were enrolled in COPDGene (phase 1, 2008-2011) and returned for a 5-year follow-up (phase 2, 2012-2016). Subjects completed questionnaires, spirometry, chest computed tomography scans, and 6-minute-walk tests at both study visits. Baseline characteristics, longitudinal change in lung function, and mortality were assessed by post-bronchodilator lung function categories: PRISm (FEV /FVC < 0.7 and FEV  < 80%), GOLD0 (FEV /FVC > 0.7 and FEV  > 80%), and GOLD1-4 (FEV /FVC < 0.7). Although the prevalence of PRISm was consistent (12.4-12.5%) at phases 1 and 2, subjects with PRISm exhibited substantial rates of transition to and from other lung function categories. Among subjects with PRISm at phase 1, 22.2% transitioned to GOLD0 and 25.1% progressed to GOLD1-4 at phase 2. Subjects with PRISm at both phase 1 and phase 2 had reduced rates of FEV decline (-27.3 ± 42.1 vs. -33.0 ± 41.7 ml/yr) and comparable proportions of normal computed tomography scans (51% vs. 52.7%) relative to subjects with stable GOLD0 spirometry. In contrast, incident PRISm exhibited accelerated rates of lung function decline. Subjects with PRISm at phase 1 had higher mortality rates relative to GOLD0 and lower rates relative to the GOLD1-4 group. PRISm is highly prevalent, is associated with increased mortality, and represents a transitional state for significant subgroups of subjects. Additional studies to characterize longitudinal progression in PRISm are warranted.
AbstractList Rationale: Increasing awareness of the prevalence and significance of Preserved Ratio Impaired Spirometry (PRISm), alternatively known as restrictive or Global Initiative for Chronic Obstructive Lung Disease (GOLD)-unclassified spirometry, has expanded the body of knowledge on cross-sectional risk factors. However, longitudinal studies of PRISm remain limited. Objectives: To examine longitudinal patterns of change in lung function, radiographic characteristics, and mortality of current and former smokers with PRISm. Methods: Current and former smokers, aged 45 to 80 years, were enrolled in COPDGene (phase 1, 2008–2011) and returned for a 5-year follow-up (phase 2, 2012–2016). Subjects completed questionnaires, spirometry, chest computed tomography scans, and 6-minute-walk tests at both study visits. Baseline characteristics, longitudinal change in lung function, and mortality were assessed by post-bronchodilator lung function categories: PRISm (FEV 1 /FVC < 0.7 and FEV 1  < 80%), GOLD0 (FEV 1 /FVC > 0.7 and FEV 1  > 80%), and GOLD1–4 (FEV 1 /FVC < 0.7). Measurements and Main Results: Although the prevalence of PRISm was consistent (12.4–12.5%) at phases 1 and 2, subjects with PRISm exhibited substantial rates of transition to and from other lung function categories. Among subjects with PRISm at phase 1, 22.2% transitioned to GOLD0 and 25.1% progressed to GOLD1–4 at phase 2. Subjects with PRISm at both phase 1 and phase 2 had reduced rates of FEV 1 decline (−27.3 ± 42.1 vs. −33.0 ± 41.7 ml/yr) and comparable proportions of normal computed tomography scans (51% vs. 52.7%) relative to subjects with stable GOLD0 spirometry. In contrast, incident PRISm exhibited accelerated rates of lung function decline. Subjects with PRISm at phase 1 had higher mortality rates relative to GOLD0 and lower rates relative to the GOLD1–4 group. Conclusions: PRISm is highly prevalent, is associated with increased mortality, and represents a transitional state for significant subgroups of subjects. Additional studies to characterize longitudinal progression in PRISm are warranted.
Rationale: Increasing awareness of the prevalence and significance of Preserved Ratio Impaired Spirometry (PRISm), alternatively known as restrictive or Global Initiative for Chronic Obstructive Lung Disease (GOLD)-unclassified spirometry, has expanded the body of knowledge on cross-sectional risk factors. However, longitudinal studies of PRISm remain limited. Objectives: To examine longitudinal patterns of change in lung function, radiographic characteristics, and mortality of current and former smokers with PRISm. Methods: Current and former smokers, aged 45 to 80 years, were enrolled in COPDGene (phase 1, 2008-2011) and returned for a 5-year follow-up (phase 2, 2012-2016). Subjects completed questionnaires, spirometry, chest computed tomography scans, and 6-minute-walk tests at both study visits. Baseline characteristics, longitudinal change in lung function, and mortality were assessed by post-bronchodilator lung function categories: PRISm (FEV1/FVC, 0.7 and FEV1,80%), GOLD0 (FEV1/FVC.0.7 and FEV1.80%), and GOLD1-4 (FEV1/FVC,0.7). Measurements and Main Results: Although the prevalence of PRISm was consistent (12.4-12.5%) at phases 1 and 2, subjects with PRISm exhibited substantial rates of transition to and from other lung function categories. Among subjects with PRISm at phase 1, 22.2% transitioned to GOLD0 and 25.1% progressed to GOLD1-4 at phase 2. Subjects with PRISm at both phase 1 and phase 2 had reduced rates of FEV1 decline (227.3642.1 vs. 233.0641.7 ml/yr) and comparable proportions of normal computed tomography scans (51% vs. 52.7%) relative to subjects with stable GOLD0 spirometry. In contrast, incident PRISm exhibited accelerated rates of lung function decline. Subjects with PRISm at phase 1 had higher mortality rates relative to GOLD0 and lower rates relative to the GOLD1-4 group. Conclusions: PRISm is highly prevalent, is associated with increased mortality, and represents a transitional state for significant subgroups of subjects. Additional studies to characterize longitudinal progression in PRISm are warranted.
Increasing awareness of the prevalence and significance of Preserved Ratio Impaired Spirometry (PRISm), alternatively known as restrictive or Global Initiative for Chronic Obstructive Lung Disease (GOLD)-unclassified spirometry, has expanded the body of knowledge on cross-sectional risk factors. However, longitudinal studies of PRISm remain limited.RATIONALEIncreasing awareness of the prevalence and significance of Preserved Ratio Impaired Spirometry (PRISm), alternatively known as restrictive or Global Initiative for Chronic Obstructive Lung Disease (GOLD)-unclassified spirometry, has expanded the body of knowledge on cross-sectional risk factors. However, longitudinal studies of PRISm remain limited.To examine longitudinal patterns of change in lung function, radiographic characteristics, and mortality of current and former smokers with PRISm.OBJECTIVESTo examine longitudinal patterns of change in lung function, radiographic characteristics, and mortality of current and former smokers with PRISm.Current and former smokers, aged 45 to 80 years, were enrolled in COPDGene (phase 1, 2008-2011) and returned for a 5-year follow-up (phase 2, 2012-2016). Subjects completed questionnaires, spirometry, chest computed tomography scans, and 6-minute-walk tests at both study visits. Baseline characteristics, longitudinal change in lung function, and mortality were assessed by post-bronchodilator lung function categories: PRISm (FEV1/FVC < 0.7 and FEV1 < 80%), GOLD0 (FEV1/FVC > 0.7 and FEV1 > 80%), and GOLD1-4 (FEV1/FVC < 0.7).METHODSCurrent and former smokers, aged 45 to 80 years, were enrolled in COPDGene (phase 1, 2008-2011) and returned for a 5-year follow-up (phase 2, 2012-2016). Subjects completed questionnaires, spirometry, chest computed tomography scans, and 6-minute-walk tests at both study visits. Baseline characteristics, longitudinal change in lung function, and mortality were assessed by post-bronchodilator lung function categories: PRISm (FEV1/FVC < 0.7 and FEV1 < 80%), GOLD0 (FEV1/FVC > 0.7 and FEV1 > 80%), and GOLD1-4 (FEV1/FVC < 0.7).Although the prevalence of PRISm was consistent (12.4-12.5%) at phases 1 and 2, subjects with PRISm exhibited substantial rates of transition to and from other lung function categories. Among subjects with PRISm at phase 1, 22.2% transitioned to GOLD0 and 25.1% progressed to GOLD1-4 at phase 2. Subjects with PRISm at both phase 1 and phase 2 had reduced rates of FEV1 decline (-27.3 ± 42.1 vs. -33.0 ± 41.7 ml/yr) and comparable proportions of normal computed tomography scans (51% vs. 52.7%) relative to subjects with stable GOLD0 spirometry. In contrast, incident PRISm exhibited accelerated rates of lung function decline. Subjects with PRISm at phase 1 had higher mortality rates relative to GOLD0 and lower rates relative to the GOLD1-4 group.MEASUREMENTS AND MAIN RESULTSAlthough the prevalence of PRISm was consistent (12.4-12.5%) at phases 1 and 2, subjects with PRISm exhibited substantial rates of transition to and from other lung function categories. Among subjects with PRISm at phase 1, 22.2% transitioned to GOLD0 and 25.1% progressed to GOLD1-4 at phase 2. Subjects with PRISm at both phase 1 and phase 2 had reduced rates of FEV1 decline (-27.3 ± 42.1 vs. -33.0 ± 41.7 ml/yr) and comparable proportions of normal computed tomography scans (51% vs. 52.7%) relative to subjects with stable GOLD0 spirometry. In contrast, incident PRISm exhibited accelerated rates of lung function decline. Subjects with PRISm at phase 1 had higher mortality rates relative to GOLD0 and lower rates relative to the GOLD1-4 group.PRISm is highly prevalent, is associated with increased mortality, and represents a transitional state for significant subgroups of subjects. Additional studies to characterize longitudinal progression in PRISm are warranted.CONCLUSIONSPRISm is highly prevalent, is associated with increased mortality, and represents a transitional state for significant subgroups of subjects. Additional studies to characterize longitudinal progression in PRISm are warranted.
Increasing awareness of the prevalence and significance of Preserved Ratio Impaired Spirometry (PRISm), alternatively known as restrictive or Global Initiative for Chronic Obstructive Lung Disease (GOLD)-unclassified spirometry, has expanded the body of knowledge on cross-sectional risk factors. However, longitudinal studies of PRISm remain limited. To examine longitudinal patterns of change in lung function, radiographic characteristics, and mortality of current and former smokers with PRISm. Current and former smokers, aged 45 to 80 years, were enrolled in COPDGene (phase 1, 2008-2011) and returned for a 5-year follow-up (phase 2, 2012-2016). Subjects completed questionnaires, spirometry, chest computed tomography scans, and 6-minute-walk tests at both study visits. Baseline characteristics, longitudinal change in lung function, and mortality were assessed by post-bronchodilator lung function categories: PRISm (FEV /FVC < 0.7 and FEV  < 80%), GOLD0 (FEV /FVC > 0.7 and FEV  > 80%), and GOLD1-4 (FEV /FVC < 0.7). Although the prevalence of PRISm was consistent (12.4-12.5%) at phases 1 and 2, subjects with PRISm exhibited substantial rates of transition to and from other lung function categories. Among subjects with PRISm at phase 1, 22.2% transitioned to GOLD0 and 25.1% progressed to GOLD1-4 at phase 2. Subjects with PRISm at both phase 1 and phase 2 had reduced rates of FEV decline (-27.3 ± 42.1 vs. -33.0 ± 41.7 ml/yr) and comparable proportions of normal computed tomography scans (51% vs. 52.7%) relative to subjects with stable GOLD0 spirometry. In contrast, incident PRISm exhibited accelerated rates of lung function decline. Subjects with PRISm at phase 1 had higher mortality rates relative to GOLD0 and lower rates relative to the GOLD1-4 group. PRISm is highly prevalent, is associated with increased mortality, and represents a transitional state for significant subgroups of subjects. Additional studies to characterize longitudinal progression in PRISm are warranted.
Author Schroeder, Joyce
MacIntyre, Neil
Fortis, Spyridon
Rozenshtein, Anna
Moore, Camille
Curtis, Jeffrey L.
Beaty, Terri
Stoel, Berend C.
Hughes, John
Sakornsakolpat, Phuwanat
Casaburi, Richard
Hanania, Nicola
Lange, Christoph
Gray, Teresa
Atik, Mustafa
McDonald, Merry-Lynn
Newell, John D.
Martinez, Carlos
Laird, Nan
Regan, Elizabeth A.
Kinney, Gregory
Murray, Susan
van Ginneken, Bram
Soler, Xavier
Sieren, Jered
Everett, Douglas
Hersh, Craig
Pratte, Katherine
Martinez, Carlos H.
Foreman, Marilyn G.
Washko, George
Wan, Emily S.
Make, Barry
Boueiz, Adel R.
van Rikxoort, Eva
Hoffman, Eric A.
Van Beek, Edwin
Crapo, James D.
Hayden, Lystra P.
Alapat, Philip
Lynch, David A.
Hobbs, Brian D.
Qiao, Dandi
Lutz, Sharon M.
Stinson, Douglas
Barr, R. Graham
Kazerooni, Ella A.
Tschirren, Juerg
Jacobson, Francine L.
Silverman, Edwin K.
Pernicano, Perry G.
Parker, Margaret M.
Strand, Matt
Hersh, Craig P.
Hetmanski, Jacqueline
Hokanson, John E.
Judy, Philip F.
Kluiber, Alex
Castaldi, Peter J.
Guy, Elizabeth
Ross, James C.
Boriek, Aladin
Crooks, Jim
Pearson, Gregory D. N.
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  fullname: Austin, John
– sequence: 96
  givenname: Belinda
  surname: D’Souza
  fullname: D’Souza, Belinda
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  surname: Thomashow
  fullname: Thomashow, Byron
– sequence: 100
  givenname: Neil
  surname: MacIntyre
  fullname: MacIntyre, Neil
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29874098$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Contributor Schroeder, Joyce
Crapo, James D
Rozenshtein, Anna
Moore, Camille
Beaty, Terri
Hughes, John
Sakornsakolpat, Phuwanat
Ross, James C
Lynch, David A
Hanania, Nicola
Newell, Jr, John D
Lange, Christoph
Gray, Teresa
Foreman, Marilyn G
Hobbs, Brian D
Atik, Mustafa
Pernicano, Perry G
Regan, Elizabeth A
McDonald, Merry-Lynn
Martinez, Carlos
Hayden, Lystra P
Laird, Nan
Kinney, Gregory
Murray, Susan
van Ginneken, Bram
Soler, Xavier
Curtis, Jeffrey L
Sieren, Jered
Everett, Douglas
Judy, Philip F
Hersh, Craig
Pratte, Katherine
Washko, George
DeMeo, Dawn L
Castaldi, Peter J
Make, Barry
van Rikxoort, Eva
Van Beek, Edwin
Martinez, Carlos H
Alapat, Philip
Hersh, Craig P
Lutz, Sharon M
Qiao, Dandi
Kazerooni, Ella A
D'Souza, Belinda
Stinson, Douglas
Young, Kendra A
Tschirren, Juerg
Boueiz, Adel R
Hokanson, John E
Stoel, Berend C
Strand, Matt
Barr, R Graham
Han, MeiLan K
Hetmanski, Jacqueline
Bowler, Russell P
Kluiber, Alex
Guy, Elizabeth
Pearson, Gregory D N
Boriek, Aladin
Crooks, Jim
Begum, Ferdouse
Won, Sungho
Jacobson, Francine L
Guntupalli, Kalpatha
Al Qaisi, Must
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spirometry mortality
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spirometry classification
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Snippet Increasing awareness of the prevalence and significance of Preserved Ratio Impaired Spirometry (PRISm), alternatively known as restrictive or Global Initiative...
Rationale: Increasing awareness of the prevalence and significance of Preserved Ratio Impaired Spirometry (PRISm), alternatively known as restrictive or Global...
Rationale: Increasing awareness of the prevalence and significance of Preserved Ratio Impaired Spirometry (PRISm), alternatively known as restrictive or Global...
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StartPage 1397
SubjectTerms Aged
Aged, 80 and over
Bronchodilators
Chronic obstructive pulmonary disease
Epidemiology
Female
Follow-Up Studies
Humans
Longitudinal Studies
Lung - physiopathology
Lung diseases
Male
Medical imaging
Middle Aged
Mortality
Original
Phenotype
Pulmonary Disease, Chronic Obstructive - diagnosis
Pulmonary Disease, Chronic Obstructive - epidemiology
Pulmonary Disease, Chronic Obstructive - physiopathology
Questionnaires
Respiratory Function Tests - methods
Respiratory Function Tests - statistics & numerical data
Risk Factors
Smokers - statistics & numerical data
Smoking
Spirometry - methods
Surveys and Questionnaires
Survival analysis
Systematic review
United States - epidemiology
Young adults
Title Longitudinal Phenotypes and Mortality in Preserved Ratio Impaired Spirometry in the COPDGene Study
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Volume 198
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