Body mass index is associated with reduced exhaled nitric oxide and higher exhaled 8-isoprostanes in asthmatics
© Komakula et al. 2007
Received: 28 December 2006
Accepted: 16 April 2007
Published: 16 April 2007
Recently, it has been shown that increasing body mass index (BMI) in asthma is associated with reduced exhaled NO. Our objective in this study was to determine if the BMI-related changes in exhaled NO differ across asthmatics and controls, and to determine if these changes are related to increased airway oxidative stress and systemic levels of leptin and adiponectin.
Observational study of the association of BMI, leptin, and adiponectin with exhaled nitric oxide (NO) and exhaled 8-isoprostanes in 67 non-smoking patients with moderate to severe persistent asthma during baseline conditions and 47 controls. Measurements included plasma levels of leptin, adiponectin, exhaled breath condensates for 8-isoprostanes, exhaled NO, pulmonary function tests, and questionnaires regarding asthma severity and control.
In asthmatics, BMI and the ratio of leptin to adiponectin were respectively associated with reduced levels of exhaled NO (β = -0.04 [95% C.I. -0.07, -0.1], p < 0.003) and (β = -0.0018 [95% C.I. -0.003, -0.00034], p = 0.01) after adjusting for confounders. Also, BMI was associated with increased levels of exhaled 8-isoprostanes (β = 0.30 [95% C.I. 0.003, 0.6], p = 0.03) after adjusting for confounders. In contrast, we did not observe these associations in the control group of healthy non-asthmatics with a similar weight distribution.
In adults with stable moderate to severe persistent asthma, but not in controls, BMI and the plasma ratio of leptin/adiponectin is associated with reduced exhaled NO. Also, BMI is associated with increased exhaled 8-isoprostanes. These results suggest that BMI in asthmatics may increase airway oxidative stress and could explain the BMI-related reductions in exhaled NO.
In recent years, there has been a parallel increase in the prevalence of both asthma and obesity. This has led to the speculation that increased BMI is a risk factor for asthma . Several cross sectional studies have shown higher odds for developing asthma among obese children and adults [2–5]; however, these studies were limited by their inability to address the direction of this association, and were susceptible to confounding factors . Prospective studies have shown that increasing BMI antedates the diagnosis of asthma incidence and bronchial hyperresponsiveness. This temporal pattern supports the idea that obesity may actually cause versus simply associate with asthma [7–11]. Further, obese asthmatics are also at increased risk of having more severe respiratory symptoms, increased emergency room visits, and poor asthma control [5, 12–16]. The mechanisms by which obesity increases asthma incidence or increases disease severity in asthmatics are unknown.
Recent experimental data suggest that obesity-related changes in adipokines could play a critical role in mediating airway inflammation and bronchial hyperresponsiveness (BHR) . Leptin, an adipokine elevated in obesity and known to induce satiety, has been shown to up-regulate various cytokines, promoting a state of chronic inflammation . Compared to saline treated mice, leptin-infused mice had higher systemic IgE levels and increased bronchial hyperresponsiveness only after ovalbumin (OVA) inhalation . In contrast, adiponectin, which is reduced in obesity, and has anti-inflammatory and antioxidant properties [19–21], has been shown to reduce BHR and decrease airway inflammation following OVA inhalation in mice . However, whether or not leptin and/or adiponectin can affect exhaled NO (nitric oxide) levels and measures of airway oxidative stress in asthmatics are unknown.
In a recent study, exhaled NO was inversely correlated with BMI in subjects with asthma, yet a potential explanation for this finding was not offered . The purpose of this study was to examine the association between BMI and adipokines (leptin and adiponectin) with exhaled NO in asthmatics and healthy controls, and to determine whether BMI-related changes in exhaled NO can be attributed to changes in airway oxidative stress by measuring exhaled 8-isoprostanes.
This study was conducted at Grady Memorial Hospital in Atlanta, Georgia with the approval of the institutional review board. Inclusion criteria included: participants 18 to 70 years of age, who were previously diagnosed with moderate to severe persistent asthma (Global Initiative for Asthma (GINA) class III – IV)  requiring treatment with inhaled corticosteroids, ≥ 12% post-bronchodilator increase in FEV1 (Forced exhalation volume in one second) and a post-bronchodilator FEV1/FVC (Forced vital capacity) ratio greater than 0.70. Exclusion criteria included: current smokers, ex-smokers who stopped smoking at least one year prior to study enrolment, or total-life smoking history > 10 pack-year, and evidence of other lung diseases or any other significant non-pulmonary co-morbidities such as congestive heart failure with ejection fraction < 50%, stable angina, chronic renal failure with serum creatinine > 2.0, documented cirrhosis, other disorders requiring steroid treatment (vasculitis, lupus, or rheumatoid arthritis), advanced cancer, or AIDS. Subjects were also excluded if they had an asthma exacerbation during the month preceding enrolment.
From the hospital personnel, we recruited healthy, non-asthmatics without any history of allergic diseases. The controls were not active smokers, and met the same smoking exclusion criteria used for the study population. Controls were selected to match the gender, race, and weight distribution of the study population.
Height, weight, and waist to hip ratios were obtained in all the participants. Participant's current level of asthma severity was classified according to the 2004 GINA guidelines into mild intermittent (Class I), mild persistent (Class II), moderate persistent (Class III), and severe persistent (Class IV) asthma. Participants also completed the Juniper asthma control questionnaire (ACQ). Atopy was based on a positive or negative skin prick test documented in the clinic records. In all patients, obstructive sleep apnea (OSA) and gastro-esophageal reflux disease (GERD) were ascertained by either medical history or use of medications to relieve GERD symptoms.
Exhaled NO was determined using an on-line continuous chemiluminescence analyzer (CDL 88 sq Michigan, USA) after overnight fasting following the American Thoracic Society guidelines prior to spirometry . Exhaled breath condensate (EBC) was collected using the Rtube, a non-invasive breath condensate collection device (Charlottesville, VA). To produce the condensate we used a metal sleeve at an initial temperature of -10 Celsius, and instructed subjects to breathe normally for 15 minutes while using a nose-clip. After the collection session, the samples were immediately stored in -70°C until analyzed. Exhaled 8-isoprostanes were determined in duplicate using an immunoassay (Cayman Chemical, Ann Arbor, MI, USA) . Pre and post-bronchodilator spirometry were determined according to ATS guidelines . Functional residual capacity (FRC) was done using a nitrogen gas dilution technique (CDL 88 sq Michigan, USA).
In overnight fasting blood samples, we determined levels of leptin and adiponectin. Adipokine levels were determined in duplicate using Luminex analysis (Linco research Inc., St. Charles Missouri) .
We used the Kruskal Wallis to compare non-normally distributed variables across BMI categories, and a t-test to compare means between asthmatics and controls. The chi square statistic was used to test the distribution of categorical variables. We modelled the association of BMI and adipokines (leptin, adiponectin, the leptin/adiponectin ratio) with the log-normal of exhaled NO or exhaled 8-isoprostanes using multivariable regression analysis. For the asthma subjects, we adjusted the model for the following potential confounders: age, gender, atopy, mean Juniper scores, degree of airflow obstruction (FEV1/FVC), diagnosis of GERD, use of long-acting beta agonists, and anti-leukotriene drugs. Given that all subjects with asthma were taking inhaled corticosteroids, this medication was not adjusted for in the model. Regression models were checked for influential points, collinearity and distribution of residuals. Statistical analysis was done using SAS 9.1 (Cary, NC), a p< 0.05 was considered significant.
Characteristics of the study population
Average age in years (Range)
48.9 (18 – 69)
Gender (% female)
Ex-smokers n (%)
Average Pack-per-year (95% C.I.)
4 (2 – 5)
Average body weight in pounds (95% C.I.)
198 (186 – 209)
Average BMI (95% C.I.)
32 (31 – 35)
Normal weight (BMI ≥ 18 ≤ 25) (%)
Overweight (BMI > 25 < 30)
Obese (BMI ≥ 30)
Average waist/hip ratio (95% C.I.)
0.87 (0.85 – 0.9)
GERD treatment (%)
Obstructive sleep apnea (%)
Average FEV1 (95% C.I.)
2.1 (2.0 – 2.3)
Average FVC (95% C.I.)
2.8 (2.6 – 3.0)
Average FEV1/FVC (95% C.I.)
0.80 (0.7 – 0.8)
Average FRC (95% C.I.)
3.2 (2.8 – 3.5)
Average Exhaled NO (95% C.I.) (ppb)*
25 (19 – 30)
Average Exhaled 8-isoprostanes (95% C.I.) (pg/ml)
11 (9.6 – 12.4)
Average Adiponectin (μg/ml) (95% C.I.)
3 (2.9 – 3.4)
Average Leptin (ng/ml) (95% C.I.)
15 (12 – 18)
The majority of participants were females, African American, obese, and 70% had a positive skin test for allergens documented in the clinic charts. Approximately a third of the population were ex-smokers, although the average amount of pack-years smoked was only 4. None of the patients had evidence of significant chronic airway obstruction. The mean post-bronchodilator FEV1 and FVC percent predicted were respectively 73% (95% C.I. 70 – 79) and 81% (95% C.I. 75 – 86).
Clinical measures of asthma severity and control
Association of BMI with exhaled NO and exhaled 8-isoprostanes
Association of leptin and adiponectin with exhaled NO and exhaled 8-isoprostanes
There were no significant associations between leptin or adiponectin with exhaled log-NO; however, the ratio of leptin (ng/ml) to adiponectin (μg/ml) (mean 0.0049 [95% C.I. 0.003–0.005]) was significantly associated with exhaled log-NO in univariate (β = -0.00035 [95% C.I. -0.002, -0.0003; p = 0.04]) and multivariate (β = -0.0018 [95% C.I. -0.003, -0.00034; p = 0.01]) analysis adjusting for confounders. The correlation between the leptin/adiponectin ratio and the log-NO was r 2 = -0.28 (p = 0.04). We did not observe significant associations between leptin, adiponectin, and their ratio with exhaled 8-isoprostanes.
Comparison between asthmatics and the control population
A total of 47 controls were recruited for the study. Their average age was 40 years (Range: 20 – 62) and was lower than in the asthmatics (p < 0.01). The mean weight was 186 lb (95% C.I. 174 – 198) and 51% were obese, 78% were female, and 88% were African American. These values did not statistically differ from the study population. Compared to the asthmatics, controls had lower exhaled NO levels (13 ppb [95% C.I. 10–15])(p< 0.01), higher FEV1 (2.7 L [95% C.I. 2.5–3]), FVC (3 L [95% C.I. 2.8–3]) and FEV1/FVC ratio (0.86 [95% C.I. 0.8–0.9]), and similar FRC (2.9 L [95% C.I. 2.5–3.3]). The levels of leptin (16 ng/ml [95% C.I. 12–20]) and adiponectin (31 μg/ml [95% C.I. 28–35]) did not differ across groups, nor did the levels of exhaled 8-isoprostanes (11 pg/ml [95% C.I. 8–13.8]).
This study evaluated the association of BMI and systemic levels of leptin and adiponectin with levels of exhaled NO and exhaled 8-isoprostanes in subjects with stable asthma and healthy controls. In subjects with asthma, BMI and the systemic leptin/adiponectin ratio were independently associated with a reduction in exhaled NO, and BMI was associated with increased levels of exhaled 8-isoprostanes. In contrast, these associations were not observed in healthy controls with a similar weight distribution. To our knowledge, this is the first study describing the association between BMI, leptin and adiponectin with exhaled NO and exhaled 8-isoprostanes in adults with asthma and in healthy controls.
Although there is compelling epidemiological evidence to support an association between obesity and asthma, plausible mechanisms for this association remain poorly understood. It has been proposed that either obesity-related changes in adipokines and/or the chronic systemic inflammation in obesity, could lead to a parallel increase in airway inflammation. Exhaled NO, a sensitive biomarker of airway inflammation in asthma, would therefore be expected to be higher in obese versus non-obese asthmatics . However, studies on BMI and exhaled NO do not clearly support this assertion. Some studies have found a positive correlation between BMI and exhaled NO in healthy adults [30, 31], whereas others have reported no differences between obese and non-obese asthmatic children . In contrast, our results showed that exhaled NO was inversely associated with BMI, after adjusting for potential confounders in stable asthmatics. Our results are similar to the findings from Barros et al, that showed a negative association between BMI and exhaled NO (r 2 = -0.32 vs. r 2 = -0.35 in our study) in 297 non-smoking asthmatics with a mean BMI of 26 (95% C.I. 25.4 – 26.5) after controlling for potential confounders . The negative association between BMI and exhaled NO does not necessarily imply that increasing BMI leads to less airway inflammation; it could imply however, that increasing BMI could lead to changes in baseline airway NO redox metabolism, through an increase in baseline airway oxidative stress. In the presence of increased reactive oxygen species, airway NO can be readily converted into reactive nitrogen species (RNS) . Because the total measured exhaled NO is the end product of NO produced – NO consumed, an increase in the RNS/NO ratio would result in lower measured exhaled NO levels .
Our data support this hypothesis by showing a significant association of BMI with exhaled 8-isoprostanes. Studies have shown that asthmatics have higher levels of exhaled 8-isoprostanes than non-asthmatics, and that levels increase with asthma severity [35–37]. In addition, BMI has been associated with higher levels of plasma and urinary levels of 8-isprostanes in men and women [38, 39]. In contrast to the inverse association between exhaled 8-isoprostanes and exhaled NO observed in our study, Montushi et al reported a positive correlation ; however, this correlation was observed in only 12 mild asthmatics that were not on inhaled corticosteroids, and was not reported for patients with more severe disease that were on inhaled corticosteroids; further, no data on body weight was provided. It is possible that the association between exhaled 8-isoprostanes with exhaled NO changes, depending on whether or not this association is determined during an asthma exacerbation or during baseline conditions.
Alternatively, increasing BMI may lead to an increase in airway oxidative stress via obesity-related changes in adipokines. For example, Leptin increases proportionately with BMI and has been shown to produce reactive oxygen species (ROS) [40, 41] through multiple mechanisms including, endothelin-1 receptor activation, reduced Nicotine Adenine Dinucleotide (NAD(p)H) oxidase activation, and production of Tumor Necrosis Factor alpha (TNF-α) [42–44]. Further, leptin levels in the bronchoalveolar lavage fluid are increased in obese mice models, and instillation of leptin in the airway is associated with acute lung injury in the presence of hyperoxia . In contrast, adiponectin is inversely associated with biomarkers of inflammation and with BMI [19, 46], and low levels of adiponectin have been associated with increased systemic oxidative stress, and reduced NO production from endothelial cells [47, 48].
It is possible that the amount of oxidative stress necessary to shift the airway redox balance towards conversion of airway nitric oxide into RNS exists only when there is a certain balance of leptin and adiponectin. For example, obesity leads to increased leptin and reduced adiponectin; this obesity-induced state of hyperleptinemia and hypoadiponectinemia is associated with increased systemic inflammation and oxidative stress [46, 49]. It is therefore possible that reaching a certain threshold of obesity-related systemic oxidative stress also results in increased airway oxidative stress. In our study, the ratio of leptin to adiponectin was not associated with exhaled levels of 8-isoprostanes, which may be indicative that other adipokine-independent pathways exist in increasing BMI-related airway oxidation.
This study has some important limiting features. First, the majority of our study population was African American, female, either overweight or obese, and previously diagnosed with moderate to severe disease. These characteristics may limit the external validity of our study, particularly since women appear to be more susceptible to obesity-mediated increase in asthma severity or asthma incidence ; further, these results may not apply to asthmatics with milder forms of asthma severity. Second, determination of causation is impossible and determination of specific mechanisms is difficult in an observational study design. Our results do provide a mechanistic hypothesis by which obesity relates to asthma; however, these results cannot provide information as to why obesity increases the risk for asthma incidence. Third, using questionnaires to evaluate conditions such as obstructive sleep apnea and GERD has a lower sensitivity; therefore, our results could be affected by residual confounding from these misclassified co-morbid conditions. We have to also consider that un-measured confounders, including a more detailed assessment of glycemic control might have important effects on the magnitude of both systemic and airway oxidative stress. Fourth, due to the fact that asthmatics were on several inhaled medications, it is difficult to determine the extent these medicines affected our results. Though all asthmatics were on inhaled corticosteroids, the various dosages and the variable effects they may have on individual patients may confound our results. However, in the study by Barros et al , the association between BMI and exhaled NO was not attenuated when adjusting for inhaled corticosteroids. Further, in the 4-state U.S. National Asthma Survey (NAS) the proportion of asthmatics using ICS is not higher among the obese. In the NAS the use of inhaled corticosteroids among 1059 normal weight asthmatics was 28%, compared to 30% in 985 overweight and 34% in 1015 obese subjects with asthma (p = 0.09) (unpublished observation) . Fifth, plasma adipokines and exhaled 8-isoprostane levels were only available in 50 and 56 out of 65 patients respectively, and could be a potential source of bias; however, we would expect this bias to be small if any, as the absence of these biological samples was not systematic, and was a consequence of random patient refusal. Sixth, although obese and overweight subjects had higher mean Juniper ACQ, we were not able to detect meaningful differences in asthma severity across BMI categories, given the size of patient population; however, our intention was to minimize differences in asthma severity across BMI categories, to assure that the association between BMI and airway biomarkers were not biased by differences in asthma severity. Seventh, our study is limited by determining airway oxidation stress using 8-isoprostanes using a commercial EIA kit which, although this method is highly specific and has been validated by gas chromatography, there have been contradictory results in the reproducibility of this essay . Further; we did not explore other airway biomarkers of inflammation and reactive nitrogen species. Finally, we did not assess directly the atopy status in the controls, and are therefore unable to determine how underlying atopy affected the comparison of NO across adults with and without asthma.
In summary, this study shows that in asthmatics, in the absence of an exacerbation, BMI and the leptin/adiponectin ratio are associated with reduced exhaled NO, and BMI is associated with increased exhaled 8-isoprostanes, possibly reflecting an increase in baseline airway oxidative stress. It remains to be elucidated whether these BMI-related changes in airway oxidation, which were determined during baseline conditions, can be associated with increased bronchial hyperresponsiveness and increased asthma severity. Because these associations were not observed among the controls, our results suggests that BMI alone is not sufficient to produce airway changes in airway NO and airway oxidative stress. Overall, these findings provide important hypothesis-generating information in understanding how obesity associates with asthma severity.
We would like to thank Dr. Roland H. Ingram Jr. for his critical input in developing this manuscript.
- Tantisira KG, Weiss ST: Complex Interaction in complex traits: Obesity and asthma. Thorax 2001, 56:ii64-ii74.PubMed CentralPubMed
- Brenner JS, Kelly CS, Wenger AD, Brich SM, Morrow AL: Asthma and obesity in adolescents: is there an association? J Asthma 2001, 38:509–515.View ArticlePubMed
- Cassol V, Rizzato TM, Teche SP, Basso DF, Centenaro DF, Maldonado M, Moraes EZ, Hirakata VN, Sole D, Menna-Barreto SS: Obesity and its relationship with asthma prevalence and severity in adolescents from southern Brazil. J Asthma 2006, 43:57–60.View ArticlePubMed
- Celedon JC, Palmer LJ, Litonjua AA, Weiss ST, Wang B, Fang Z, Xu X: Body mass index and asthma in adults in families of subjects with asthma in Anqing, China. Am J Respir Crit Care Med 2001, 164:1835–1840.View ArticlePubMed
- Luder E, Melnik TA, DiMaio M: Association of being overweight with greater asthma symptoms in inner city black and Hispanic children. J Pediatr 1998, 132:699–703.View ArticlePubMed
- Shore SA, Johnston RA: Obesity and asthma. Pharmacol Ther 2006, 110:83–102.View ArticlePubMed
- Camargo CA Jr., Weiss ST, Zhang S, Willett WC, Speizer FE: Prospective study of body mass index, weight change, and risk of adult-onset asthma in women. Arch Intern Med 1999, 159:2582–2588.View ArticlePubMed
- Beckett WS, Jacobs DR Jr., Yu X, Iribarren C, Williams OD: Asthma is associated with weight gain in females but not males, independent of physical activity. Am J Respir Crit Care Med 2001, 164:2045–2050.View ArticlePubMed
- Chen Y, Dales R, Krewski D, Breithaupt K: Increased effects of smoking and obesity on asthma among female Canadians: the National Population Health Survey, 1994–1995. Am J Epidemiol 1999, 150:255–262.View ArticlePubMed
- Stanley AH, Demissie K, Rhoads GG: Asthma development with obesity exposure: observations from the cohort of the National Health and Nutrition Evaluation Survey Epidemiologic Follow-up Study (NHEFS). J Asthma 2005, 42:97–99.View ArticlePubMed
- Nystad W, Meyer HE, Nafstad P, Tverdal A, Engeland A: Body mass index in relation to adult asthma among 135,000 Norwegian men and women. Am J Epidemiol 2004, 160:969–976.View ArticlePubMed
- Akerman MJ, Calacanis CM, Madsen MK: Relationship between asthma severity and obesity. J Asthma 2004, 41:521–526.View ArticlePubMed
- Belamarich PF, Luder E, Kattan M, Mitchell H, Islam S, Lynn H, Crain EF: Do obese inner-city children with asthma have more symptoms than nonobese children with asthma? Pediatrics 2000, 106:1436–1441.View ArticlePubMed
- von Mutius E, Schwartz J, Neas LM, Dockery D, Weiss ST: Relation of body mass index to asthma and atopy in children: the National Health and Nutrition Examination Study III. Thorax 2001, 56:835–838.PubMed CentralView ArticlePubMed
- Varraso R, Siroux V, Maccario J, Pin I, Kauffmann F: Asthma severity is associated with body mass index and early menarche in women. Am J Respir Crit Care Med 2005, 171:334–339.View ArticlePubMed
- Thomson CC, Clark S, Camargo CA Jr.: Body mass index and asthma severity among adults presenting to the emergency department. Chest 2003, 124:795–802.View ArticlePubMed
- Loffreda S, Yang SQ, Lin HZ, Karp CL, Brengman ML, Wang DJ, Klein AS, Bulkley GB, Bao C, Noble PW, Lane MD, Diehl AM: Leptin regulates proinflammatory immune responses. FASEB J 1998, 12:57–65.PubMed
- Shore SA, Schwartzman IN, Mellema MS, Flynt L, Imrich A, Johnston RA: Effect of leptin on allergic airway responses in mice. J Allergy Clin Immunol 2005, 115:103–109.View ArticlePubMed
- Engeli S, Feldpausch M, Gorzelniak K, Hartwig F, Heintze U, Janke J, Mohlig M, Pfeiffer AF, Luft FC, Sharma AM: Association between adiponectin and mediators of inflammation in obese women. Diabetes 2003, 52:942–947.View ArticlePubMed
- Katsuki A, Suematsu M, Gabazza EC, Murashima S, Nakatani K, Togashi K, Yano Y, Adachi Y, Sumida Y: Increased oxidative stress is associated with decreased circulating levels of adiponectin in Japanese metabolically obese, normal-weight men with normal glucose tolerance. Diabetes Res Clin Pract 2006, 73:310–314.View ArticlePubMed
- Nakanishi S, Yamane K, Kamei N, Nojima H, Okubo M, Kohno N: A protective effect of adiponectin against oxidative stress in Japanese Americans: the association between adiponectin or leptin and urinary isoprostane. Metabolism 2005, 54:194–199.View ArticlePubMed
- Shore S, Terry RD, Flynt L, Xu A, Hug C: Adiponectin attenuates allergen-induced airway inflammation and hyperresponsiveness in mice. J Allergy Clin Immunol 2006., In press:
- Barros R, Moreira A, Fonseca J, Moreira P, Fernandes L, Ferraz de Oliveira J, Delagado L, Castel-Branco MG: Obesity and airway inflammation in asthma. J Allergy Clin Immunol 2006, 117:1501–1502.View ArticlePubMed
- GINA (Global Initiative for Asthma) Workshop Report, Global Strategy for Asthma Management and Prevention [http://www.ginasthma.com/Guidelineitem.asp] 2004, 74–75.
- Juniper EF, O'Byrne PM, Guyatt GH, Ferrie PJ, King DR: Development and validation of a questionnaire to measure asthma control. Eur Respir J 1999, 14:902–907.View ArticlePubMed
- ATS/ERS Recommendations for Standardized Procedures for the Online and Offline Measurement of Exhaled Lower Respiratory Nitric Oxide and Nasal Nitric Oxide, 2005Am J Resp Crit Care Med 2005, 171:912–930.
- Carpagnano GE, Kharitonov SA, Foschino-Barbaro MP, Resta O, Gramiccioni E, Barnes PJ: Supplementary oxygen in healthy subjects and those with COPD increases oxidative stress and airway inflammation. Thorax 2004, 59:1016–1019.PubMed CentralView ArticlePubMed
- Standardization of Spirometry, 1994 Update. American Thoracic SocietyAm J Resp Crit Care Med 1995, 152:1107–1136.
- Liu MY, Xydakis AM, Hoogeveen RC, Jones PH, Smith EO, Nelson KW, Ballantyne CM: Multiplexed analysis of biomarkers related to obesity and the metabolic syndrome in human plasma, using the Luminex-100 system. Clin Chem 2005, 51:1102–1109.View ArticlePubMed
- KM DWG, Van der Ent CK, Prins I, Tersmette JM, Uiterwaal CS: Exhaled nitric oxide: the missing link between asthma and obesity? J Allergy Clin Immunol 2005, 115:419–420.View Article
- Tsang KW, Ip SK, Leung R, Tipoe GL, Chan SL, Shum IH, Ip MS, Yan C, Fung PC, Chan-Yeung M, Lam W: Exhaled nitric oxide: the effects of age, gender and body size. Lung 2001, 179:83–91.View ArticlePubMed
- Leung TF, Li CY, Lam CW, Au CS, Yung E, Chan IH, Wong GW, Fok TF: The relation between obesity and asthmatic airway inflammation. Pediatr Allergy Immunol 2004, 15:344–350.View ArticlePubMed
- Gow AJ: The biological chemistry of nitric oxide as it pertains to the extrapulmonary effects of inhaled nitric oxide. Proc Am Thorac Soc 2006, 3:150–152.PubMed CentralView ArticlePubMed
- Nguyen TA, Woo-Park J, Hess M, Goins M, Urban P, Vaughan J, Smith A, Hunt J: Assaying all of the nitrogen oxides in breath modifies the interpretation of exhaled nitric oxide. Vascul Pharmacol 2005, 43:379–384.View ArticlePubMed
- Antczak A, Montuschi P, Kharitonov S, Gorski P, Barnes PJ: Increased exhaled cysteinyl-leukotrienes and 8-isoprostane in aspirin-induced asthma. Am J Respir Crit Care Med 2002, 166:301–306.View ArticlePubMed
- Baraldi E, Ghiro L, Piovan V, Carraro S, Ciabattoni G, Barnes PJ, Montuschi P: Increased exhaled 8-isoprostane in childhood asthma. Chest 2003, 124:25–31.View ArticlePubMed
- Montuschi P, Corradi M, Ciabattoni G, Nightingale J, Kharitonov SA, Barnes PJ: Increased 8-isoprostane, a marker of oxidative stress, in exhaled condensate of asthma patients. Am J Respir Crit Care Med 1999, 160:216–220.View ArticlePubMed
- Keaney JF Jr., Larson MG, Vasan RS, Wilson PW, Lipinska I, Corey D, Massaro JM, Sutherland P, Vita JA, Benjamin EJ: Obesity and systemic oxidative stress: clinical correlates of oxidative stress in the Framingham Study. Arterioscler Thromb Vasc Biol 2003, 23:434–439.View ArticlePubMed
- Urakawa H, Katsuki A, Sumida Y, Gabazza EC, Murashima S, Morioka K, Maruyama N, Kitagawa N, Tanaka T, Hori Y, Nakatani K, Yano Y, Adachi Y: Oxidative stress is associated with adiposity and insulin resistance in men. J Clin Endocrinol Metab 2003, 88:4673–4676.View ArticlePubMed
- Beltowski J, Wojcicka G, Jamroz A: Leptin decreases plasma paraoxonase 1 (PON1) activity and induces oxidative stress: the possible novel mechanism for proatherogenic effect of chronic hyperleptinemia. Atherosclerosis 2003, 170:21–29.View ArticlePubMed
- Bouloumie A, Marumo T, Lafontan M, Busse R: Leptin induces oxidative stress in human endothelial cells. FASEB J 1999, 13:1231–1238.PubMed
- Shen J, Sakaida I, Uchida K, Terai S, Okita K: Leptin enhances TNF-alpha production via p38 and JNK MAPK in LPS-stimulated Kupffer cells. Life Sci 2005, 77:1502–1515.View ArticlePubMed
- Xu FP, Chen MS, Wang YZ, Yi Q, Lin SB, Chen AF, Luo JD: Leptin induces hypertrophy via endothelin-1-reactive oxygen species pathway in cultured neonatal rat cardiomyocytes. Circulation 2004, 110:1269–1275.View ArticlePubMed
- Dong F, Zhang X, Ren J: Leptin regulates cardiomyocyte contractile function through endothelin-1 receptor-NADPH oxidase pathway. Hypertension 2006, 47:222–229.View ArticlePubMed
- Bellmeyer A, Martino JM, Chandel NS, Scott Budinger GR, Dean DA, Mutlu GM: Leptin Resistance Protects Mice from Hyperoxia-induced Acute Lung Injury. Am J Respir Crit Care Med 2007, 175:587–594.PubMed CentralView ArticlePubMed
- Ronti T, Lupattelli G, Mannarino E: The endocrine function of adipose tissue: an update. Clin Endocrinol (Oxf) 2006, 64:355–365.
- Hattori S, Hattori Y, Kasai K: Hypoadiponectinemia is caused by chronic blockade of nitric oxide synthesis in rats. Metabolism 2005, 54:482–487.View ArticlePubMed
- Hattori Y, Akimoto K, Gross SS, Hattori S, Kasai K: Angiotensin-II-induced oxidative stress elicits hypoadiponectinaemia in rats. Diabetologia 2005, 48:1066–1074.View ArticlePubMed
- Ouchi N, Kihara S, Funahashi T, Matsuzawa Y, Walsh K: Obesity, adiponectin and vascular inflammatory disease. Curr Opin Lipidol 2003, 14:561–566.View ArticlePubMed
- National Asthma Survey [http://www.cdc.gov/nchs/about/major/slaits/nas.htm] 2007.
- Horvath I, Hunt J, Barnes PJ, Alving K, Antczak A, Baraldi E, Becher G, van Beurden WJ, Corradi M, Dekhuijzen R, Dweik RA, Dwyer T, Effros R, Erzurum S, Gaston B, Gessner C, Greening A, Ho LP, Hohlfeld J, Jobsis Q, Laskowski D, Loukides S, Marlin D, Montuschi P, Olin AC, Redington AE, Reinhold P, van Rensen EL, Rubinstein I, Silkoff P, Toren K, Vass G, Vogelberg C, Wirtz H: Exhaled breath condensate: methodological recommendations and unresolved questions. Eur Respir J 2005, 26:523–548.View ArticlePubMed
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