Body Mass and Glucocorticoid Response in Asthma

Obesity may alter glucocorticoid response in asthma. To evaluate the relationship between body mass index (BMI, kg/m(2)) and glucocorticoid response in subjects with and without asthma. Nonsmoking adult subjects underwent characterization of lung function, BMI, and spirometric response to prednisone...

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Published inAmerican journal of respiratory and critical care medicine Vol. 178; no. 7; pp. 682 - 687
Main Authors Sutherland, E. Rand, Goleva, Elena, Strand, Matthew, Beuther, David A, Leung, Donald Y. M
Format Journal Article
LanguageEnglish
Published New York, NY Am Thoracic Soc 01.10.2008
American Lung Association
American Thoracic Society
Subjects
Online AccessGet full text
ISSN1073-449X
1535-4970
1535-4970
DOI10.1164/rccm.200801-076OC

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Abstract Obesity may alter glucocorticoid response in asthma. To evaluate the relationship between body mass index (BMI, kg/m(2)) and glucocorticoid response in subjects with and without asthma. Nonsmoking adult subjects underwent characterization of lung function, BMI, and spirometric response to prednisone. Dexamethasone (DEX, 10(-6) M)-induced mitogen-activated protein kinase phosphatase-1 (MKP-1) and baseline tumor necrosis factor (TNF)-alpha expression were evaluated by polymerase chain reaction in peripheral blood mononuclear cells (PBMCs) and bronchoalveolar lavage cells. The relationship between BMI and expression of MKP-1 and TNF-alpha was analyzed. A total of 45 nonsmoking adults, 33 with asthma (mean [SD] FEV(1)% of 70.7 [9.8]%) and 12 without asthma were enrolled. DEX-induced PBMC MKP-1 expression was reduced in overweight/obese versus lean patients with asthma, with mean (+/- SEM) fold-induction of 3.11 (+/-0.46) versus 5.27 (+/-0.66), respectively (P = 0.01). In patients with asthma, regression analysis revealed a -0.16 (+/-0.08)-fold decrease in DEX-induced MKP-1 per unit BMI increase (P = 0.04). PBMC TNF-alpha expression increased as BMI increased in subjects with asthma, with a 0.27 unit increase in log (TNF-alpha [ng/ml]) per unit BMI increase (P = 0.01). The ratio of PBMC log (TNF-alpha):DEX-induced MKP-1 also increased as BMI increased in patients with asthma (+0.09 +/- 0.02; P = 0.004). In bronchoalveolar lavage cells, DEX-induced MKP-1 expression was also reduced in overweight/obese versus lean patients with asthma (1.36 +/- 0.09-fold vs. 1.76 +/- 0.15-fold induction; P = 0.05). Similar findings were not observed in control subjects without asthma. Elevated BMI is associated with blunted in vitro response to dexamethasone in overweight and obese patients with asthma.
AbstractList Obesity may alter glucocorticoid response in asthma. To evaluate the relationship between body mass index (BMI, kg/m(2)) and glucocorticoid response in subjects with and without asthma. Nonsmoking adult subjects underwent characterization of lung function, BMI, and spirometric response to prednisone. Dexamethasone (DEX, 10(-6) M)-induced mitogen-activated protein kinase phosphatase-1 (MKP-1) and baseline tumor necrosis factor (TNF)-alpha expression were evaluated by polymerase chain reaction in peripheral blood mononuclear cells (PBMCs) and bronchoalveolar lavage cells. The relationship between BMI and expression of MKP-1 and TNF-alpha was analyzed. A total of 45 nonsmoking adults, 33 with asthma (mean [SD] FEV(1)% of 70.7 [9.8]%) and 12 without asthma were enrolled. DEX-induced PBMC MKP-1 expression was reduced in overweight/obese versus lean patients with asthma, with mean (+/- SEM) fold-induction of 3.11 (+/-0.46) versus 5.27 (+/-0.66), respectively (P = 0.01). In patients with asthma, regression analysis revealed a -0.16 (+/-0.08)-fold decrease in DEX-induced MKP-1 per unit BMI increase (P = 0.04). PBMC TNF-alpha expression increased as BMI increased in subjects with asthma, with a 0.27 unit increase in log (TNF-alpha [ng/ml]) per unit BMI increase (P = 0.01). The ratio of PBMC log (TNF-alpha):DEX-induced MKP-1 also increased as BMI increased in patients with asthma (+0.09 +/- 0.02; P = 0.004). In bronchoalveolar lavage cells, DEX-induced MKP-1 expression was also reduced in overweight/obese versus lean patients with asthma (1.36 +/- 0.09-fold vs. 1.76 +/- 0.15-fold induction; P = 0.05). Similar findings were not observed in control subjects without asthma. Elevated BMI is associated with blunted in vitro response to dexamethasone in overweight and obese patients with asthma.
Obesity may alter glucocorticoid response in asthma. To evaluate the relationship between body mass index (BMI, kg/m(2)) and glucocorticoid response in subjects with and without asthma. Nonsmoking adult subjects underwent characterization of lung function, BMI, and spirometric response to prednisone. Dexamethasone (DEX, 10(-6) M)-induced mitogen-activated protein kinase phosphatase-1 (MKP-1) and baseline tumor necrosis factor (TNF)-alpha expression were evaluated by polymerase chain reaction in peripheral blood mononuclear cells (PBMCs) and bronchoalveolar lavage cells. The relationship between BMI and expression of MKP-1 and TNF-alpha was analyzed. A total of 45 nonsmoking adults, 33 with asthma (mean [SD] FEV(1)% of 70.7 [9.8]%) and 12 without asthma were enrolled. DEX-induced PBMC MKP-1 expression was reduced in overweight/obese versus lean patients with asthma, with mean (+/- SEM) fold-induction of 3.11 (+/-0.46) versus 5.27 (+/-0.66), respectively (P = 0.01). In patients with asthma, regression analysis revealed a -0.16 (+/-0.08)-fold decrease in DEX-induced MKP-1 per unit BMI increase (P = 0.04). PBMC TNF-alpha expression increased as BMI increased in subjects with asthma, with a 0.27 unit increase in log (TNF-alpha [ng/ml]) per unit BMI increase (P = 0.01). The ratio of PBMC log (TNF-alpha):DEX-induced MKP-1 also increased as BMI increased in patients with asthma (+0.09 +/- 0.02; P = 0.004). In bronchoalveolar lavage cells, DEX-induced MKP-1 expression was also reduced in overweight/obese versus lean patients with asthma (1.36 +/- 0.09-fold vs. 1.76 +/- 0.15-fold induction; P = 0.05). Similar findings were not observed in control subjects without asthma. Elevated BMI is associated with blunted in vitro response to dexamethasone in overweight and obese patients with asthma.
Rationale: Obesity may alter glucocorticoid response in asthma. Objectives: To evaluate the relationship between body mass index (BMI, kg/m2) and glucocorticoid response in subjects with and without asthma. Methods: Nonsmoking adult subjects underwent characterization of lung function, BMI, and spirometric response to prednisone. Dexamethasone (DEX, 10−6 M)-induced mitogen-activated protein kinase phosphatase-1 (MKP-1) and baseline tumor necrosis factor (TNF)-α expression were evaluated by polymerase chain reaction in peripheral blood mononuclear cells (PBMCs) and bronchoalveolar lavage cells. The relationship between BMI and expression of MKP-1 and TNF-α was analyzed. Measurements and Main Results: A total of 45 nonsmoking adults, 33 with asthma (mean [SD] FEV1% of 70.7 [9.8]%) and 12 without asthma were enrolled. DEX-induced PBMC MKP-1 expression was reduced in overweight/obese versus lean patients with asthma, with mean (± SEM) fold-induction of 3.11 (±0.46) versus 5.27 (±0.66), respectively (P = 0.01). In patients with asthma, regression analysis revealed a −0.16 (±0.08)-fold decrease in DEX-induced MKP-1 per unit BMI increase (P = 0.04). PBMC TNF-α expression increased as BMI increased in subjects with asthma, with a 0.27 unit increase in log (TNF-α [ng/ml]) per unit BMI increase (P = 0.01). The ratio of PBMC log (TNF-α):DEX-induced MKP-1 also increased as BMI increased in patients with asthma (+0.09 ± 0.02; P = 0.004). In bronchoalveolar lavage cells, DEX-induced MKP-1 expression was also reduced in overweight/obese versus lean patients with asthma (1.36 ± 0.09-fold vs. 1.76 ± 0.15-fold induction; P = 0.05). Similar findings were not observed in control subjects without asthma. Conclusions: Elevated BMI is associated with blunted in vitro response to dexamethasone in overweight and obese patients with asthma.
Obesity may alter glucocorticoid response in asthma.RATIONALEObesity may alter glucocorticoid response in asthma.To evaluate the relationship between body mass index (BMI, kg/m(2)) and glucocorticoid response in subjects with and without asthma.OBJECTIVESTo evaluate the relationship between body mass index (BMI, kg/m(2)) and glucocorticoid response in subjects with and without asthma.Nonsmoking adult subjects underwent characterization of lung function, BMI, and spirometric response to prednisone. Dexamethasone (DEX, 10(-6) M)-induced mitogen-activated protein kinase phosphatase-1 (MKP-1) and baseline tumor necrosis factor (TNF)-alpha expression were evaluated by polymerase chain reaction in peripheral blood mononuclear cells (PBMCs) and bronchoalveolar lavage cells. The relationship between BMI and expression of MKP-1 and TNF-alpha was analyzed.METHODSNonsmoking adult subjects underwent characterization of lung function, BMI, and spirometric response to prednisone. Dexamethasone (DEX, 10(-6) M)-induced mitogen-activated protein kinase phosphatase-1 (MKP-1) and baseline tumor necrosis factor (TNF)-alpha expression were evaluated by polymerase chain reaction in peripheral blood mononuclear cells (PBMCs) and bronchoalveolar lavage cells. The relationship between BMI and expression of MKP-1 and TNF-alpha was analyzed.A total of 45 nonsmoking adults, 33 with asthma (mean [SD] FEV(1)% of 70.7 [9.8]%) and 12 without asthma were enrolled. DEX-induced PBMC MKP-1 expression was reduced in overweight/obese versus lean patients with asthma, with mean (+/- SEM) fold-induction of 3.11 (+/-0.46) versus 5.27 (+/-0.66), respectively (P = 0.01). In patients with asthma, regression analysis revealed a -0.16 (+/-0.08)-fold decrease in DEX-induced MKP-1 per unit BMI increase (P = 0.04). PBMC TNF-alpha expression increased as BMI increased in subjects with asthma, with a 0.27 unit increase in log (TNF-alpha [ng/ml]) per unit BMI increase (P = 0.01). The ratio of PBMC log (TNF-alpha):DEX-induced MKP-1 also increased as BMI increased in patients with asthma (+0.09 +/- 0.02; P = 0.004). In bronchoalveolar lavage cells, DEX-induced MKP-1 expression was also reduced in overweight/obese versus lean patients with asthma (1.36 +/- 0.09-fold vs. 1.76 +/- 0.15-fold induction; P = 0.05). Similar findings were not observed in control subjects without asthma.MEASUREMENTS AND MAIN RESULTSA total of 45 nonsmoking adults, 33 with asthma (mean [SD] FEV(1)% of 70.7 [9.8]%) and 12 without asthma were enrolled. DEX-induced PBMC MKP-1 expression was reduced in overweight/obese versus lean patients with asthma, with mean (+/- SEM) fold-induction of 3.11 (+/-0.46) versus 5.27 (+/-0.66), respectively (P = 0.01). In patients with asthma, regression analysis revealed a -0.16 (+/-0.08)-fold decrease in DEX-induced MKP-1 per unit BMI increase (P = 0.04). PBMC TNF-alpha expression increased as BMI increased in subjects with asthma, with a 0.27 unit increase in log (TNF-alpha [ng/ml]) per unit BMI increase (P = 0.01). The ratio of PBMC log (TNF-alpha):DEX-induced MKP-1 also increased as BMI increased in patients with asthma (+0.09 +/- 0.02; P = 0.004). In bronchoalveolar lavage cells, DEX-induced MKP-1 expression was also reduced in overweight/obese versus lean patients with asthma (1.36 +/- 0.09-fold vs. 1.76 +/- 0.15-fold induction; P = 0.05). Similar findings were not observed in control subjects without asthma.Elevated BMI is associated with blunted in vitro response to dexamethasone in overweight and obese patients with asthma.CONCLUSIONSElevated BMI is associated with blunted in vitro response to dexamethasone in overweight and obese patients with asthma.
Author Goleva, Elena
Strand, Matthew
Leung, Donald Y. M
Beuther, David A
Sutherland, E. Rand
AuthorAffiliation 1 Department of Medicine, National Jewish Medical and Research Center, Denver, Colorado; 2 Department of Medicine, University of Colorado, Denver, Colorado; 3 Department of Pediatrics, and 4 Division of Biostatistics, National Jewish Medical and Research Center, Denver, Colorado; and 5 Department of Preventive Medicine and Biometrics, and 6 Department of Pediatrics, University of Colorado, Denver, Colorado
AuthorAffiliation_xml – name: 1 Department of Medicine, National Jewish Medical and Research Center, Denver, Colorado; 2 Department of Medicine, University of Colorado, Denver, Colorado; 3 Department of Pediatrics, and 4 Division of Biostatistics, National Jewish Medical and Research Center, Denver, Colorado; and 5 Department of Preventive Medicine and Biometrics, and 6 Department of Pediatrics, University of Colorado, Denver, Colorado
Author_xml – sequence: 1
  fullname: Sutherland, E. Rand
– sequence: 2
  fullname: Goleva, Elena
– sequence: 3
  fullname: Strand, Matthew
– sequence: 4
  fullname: Beuther, David A
– sequence: 5
  fullname: Leung, Donald Y. M
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Issue 7
Keywords Lung disease
Obesity
Intensive care
Respiratory disease
therapy
Nutrition disorder
Glucocorticoid
Asthma
Treatment
Bronchus disease
Obstructive pulmonary disease
Nutritional status
Resuscitation
Language English
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Supported by National Institutes of Health grants HL090982 (E.R.S.), AI070140 and HL36577 (D.Y.M.L.), and M01RR000051.
Correspondence and requests for reprints should be addressed to E. Rand Sutherland, M.D., M.P.H., National Jewish Health Center, 1400 Jackson Street, J-220 Denver, CO 80206. E-mail: sutherlande@njc.org
Originally Published in Press as DOI: 10.1164/rccm.200801-076OC on July 17, 2008
Conflict of Interest Statement: E.R.S. served as an advisor or consultant to Dey, GlaxoSmithKline, and Schering-Plough, and received grant funding from Dey, GlaxoSmithKline, and Novartis between 2005 and 2008. E.G. does not have a financial relationship with a commercial entity that has an interest in the subject of this manuscript. M.S. does not have a financial relationship with a commercial entity that has an interest in the subject of this manuscript. D.A.B. has received $25,000 in investigator-initiated grant support from Merck & Co. D.Y.M.L. does not have a financial relationship with a commercial entity that has an interest in the subject of this manuscript.
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PublicationTitle American journal of respiratory and critical care medicine
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American Lung Association
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Snippet Obesity may alter glucocorticoid response in asthma. To evaluate the relationship between body mass index (BMI, kg/m(2)) and glucocorticoid response in...
Obesity may alter glucocorticoid response in asthma. To evaluate the relationship between body mass index (BMI, kg/m(2)) and glucocorticoid response in...
Obesity may alter glucocorticoid response in asthma.RATIONALEObesity may alter glucocorticoid response in asthma.To evaluate the relationship between body mass...
Rationale: Obesity may alter glucocorticoid response in asthma. Objectives: To evaluate the relationship between body mass index (BMI, kg/m2) and...
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SubjectTerms A. Asthma and Allergy
Adult
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Asthma - complications
Asthma - drug therapy
Biological and medical sciences
Body Mass Index
Bronchoalveolar Lavage Fluid - cytology
Case-Control Studies
Chronic obstructive pulmonary disease, asthma
Dexamethasone - pharmacology
Dual Specificity Phosphatase 1 - drug effects
Female
Glucocorticoids - pharmacology
Humans
In Vitro Techniques
Intensive care medicine
Leukocytes, Mononuclear - drug effects
Leukocytes, Mononuclear - metabolism
Male
Medical sciences
Middle Aged
Obesity - complications
Pneumology
Tumor Necrosis Factor-alpha - drug effects
Title Body Mass and Glucocorticoid Response in Asthma
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