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 in | American journal of respiratory and critical care medicine Vol. 178; no. 7; pp. 682 - 687 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Am Thoracic Soc
01.10.2008
American Lung Association American Thoracic Society |
Subjects | |
Online Access | Get full text |
ISSN | 1073-449X 1535-4970 1535-4970 |
DOI | 10.1164/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. |
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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 |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20706267$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/18635892$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1164/rccm.200303-403WS 10.1196/annals.1321.007 10.4049/jimmunol.169.10.5934 10.1172/JCI116963 10.1164/ajrccm.159.1.9712108 10.1164/rccm.200611-1717OC 10.1016/j.jaci.2005.02.023 10.1183/09031936.05.00035205 10.1016/j.jaci.2004.08.005 10.1093/emboj/20.24.7108 10.1016/S1081-1206(10)61707-3 10.1164/ajrccm.162.6.ats9-00 10.1152/ajpendo.00471.2005 10.1172/JCI200319246 10.1038/clpt.1990.167 10.1056/NEJMoa050580 10.1172/JCI117936 10.1164/rccm.200507-1046OC 10.1074/jbc.M411760200 10.1183/09031936.06.00077205 10.1073/pnas.121455098 10.1016/j.rmed.2007.06.031 10.4049/jimmunol.171.6.3262 10.1152/japplphysiol.00847.2006 10.1183/09031936.05.00034805 10.1016/j.jaci.2006.10.025 10.1164/ajrccm.161.1.ats11-99 10.1172/JCI20514 10.1172/JCI117899 10.1164/rccm.200602-231PP 10.1172/JCI118504 10.1164/rccm.200304-503OC 10.1677/joe.0.1780005 10.1016/j.steroids.2005.02.006 |
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Keywords | Lung disease Obesity Intensive care Respiratory disease therapy Nutrition disorder Glucocorticoid Asthma Treatment Bronchus disease Obstructive pulmonary disease Nutritional status Resuscitation |
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Notes | SourceType-Scholarly Journals-1 ObjectType-News-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 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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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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Title | Body Mass and Glucocorticoid Response in Asthma |
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