Abstract
Background
Established indicators of central obesity include waist circumference, waist to height ratio and the conicity index. Studies utilizing such measures (as opposed to body mass index (BMI) percentiles) to characterize the association between obesity and asthma are lacking despite the fact that these measures have been shown to be most relevant for many other chronic diseases.
Objectives
To examine measures assessing the distribution of obesity in the context of childhood allergic rhinitis and asthma, and to elucidate the association of obesity, including central obesity, with allergic asthma in children.
Methods
Children with allergic rhinitis with (cases) or without (controls) asthma were recruited. BMI percentiles were derived using national growth charts. Waist circumference, waist to height ratio, and conicity index were obtained.
Results
Central obesity was associated with asthma, asthma severity, lower lung function, and reduced atopy in asthmatics.
Conclusion
Measures of central obesity are more associated with the presence of asthma and asthma severity in children with allergic rhinitis when compared to standard BMI measures.
Clinical Implication
Current practices of measuring weight and height in pediatric clinics that treat children with allergic rhinitis should include waist circumference measurements to better assess obesity and asthma risk.
Keywords: Asthma, Obesity, Children, BMI percentiles, Waist circumference
Introduction
Obesity is a major public health problem that often begins in childhood and is increasing at an alarming rate1. Obesity affects multiple target organs and is associated with other diseases, including asthma2. The parallel rise in the prevalence of asthma and obesity suggests that these disorders may be linked3, 4. Compared with non-asthmatics, BMI in adults with asthma is 44–48% higher across three cross-sectional US health surveys5. Further support for an association between asthma and obesity is provided by prospective studies, which show that risk for asthma increases with increasing BMI6–9. Indeed, a recent meta-analysis confirmed that obesity is a strong risk factor for incident asthma10; risk for asthma increased from being overweight to obese in a dose-response fashion10. Notably, as obese asthmatics lose weight, their asthma symptoms and lung function improve11.
While the above studies are performed in adults, childhood studies that investigate the relationship between asthma and obesity are few and contradictory12–16. Several studies report increased prevalence of obesity in asthmatics5, 8, 17, while others fail to find such a relationship18–20. Inconsistent findings may result in part from the inadequate classification of obesity phenotypes.
One of the most widely used tools to screen for obesity is BMI. However, BMI is an indicator of relative body weight that may not adequately reflect fat distribution21, and may underestimate or overestimate obesity in children since wide variations in body fat may occur within the same BMI percentile group22. Also, children undergo complex growth-related shifts in fat distribution independent of BMI23. Thus, individuals classified as obese using BMI may not be classified as obese using more direct measures of body fat. There is strong agreement that health risks for obesity are most associated with fat distribution rather than body weight24. Thus, alternative measures that are more reflective of fat distribution may better identify obese children at increased risk for asthma22.
Alternative measures that account for fat distribution include waist circumference, a measure of abdominal (central) obesity that, compared to BMI percentiles, better predicts risk for some diseases such as cardiovascular disease25. Similarly, waist to height ratio26 and conicity index27, 28 have been found to be more sensitive than BMI in predicting risk for cardiovascular disease. To date, these measures are rarely used in childhood studies and even less frequently used to assess obesity in childhood asthma. This study was conducted to compare these alternative measures with BMI percentiles in order to determine how they differ in their classification of obesity and in their association with asthma severity in children with allergic rhinitis.
Methods
Subjects
Children ages 5–18 years were sequentially recruited from the outpatient Allergy/Immunology clinics at Cincinnati Children’s Hospital Medical Center (CCHMC), N=1123. Exclusion criteria included: 1) co-morbid lung condition; 2) chronic disease other than allergic disorders; and 3) dependency on an immunosuppressive agent for a medical condition other than asthma. Detailed questionnaires to collect medical information were completed by the parent/guardian accompanying the child during the clinic visit29–31. Height(m), weight(kg), and waist circumference(cm) were measured during the clinic visit by a trained professional32. Of the 1123 children, 482 children had a waist circumference measurement. There were no significant differences in race, age, or annual household income between children without a waist circumference measurement and those with a waist circumference measurement. There was a borderline difference in gender among children without a waist circumference measurement (46.6% female) compared with those with a measurement (41% female) (p=0.05).
Outcome definitions
Pulmonary function testing was performed and asthma was diagnosed according to the American Thoracic Society guidelines 33. Asthma severity was designated based on lung function (FEV1) and frequency of symptoms, and was classified into mild, moderate or severe31.
Allergy skin prick testing (SPT)
Allergic sensitization was determined in all subjects by SPTs to eleven aeroallergens (mold mixes (2), grass mix, ragweed (giant and short), tree pollen mixes (2), weed mix, dust mite mix, cat, dog, and cockroach mix) common to the Ohio River Valley (Hollister-Stier). Skin prick testing was performed using GREERPick™ (Greer Laboratories, Lenoir, North Carolina). Sensitization was defined as present when there was wheal greater than 3 mm and greater than the saline negative control. Histatrol® (Center Laboratories, Port Washington, NY) was used as the positive control. A child was considered to have allergic rhinitis if they had rhinitis as well as a positive SPT to at least one aeroallergen. The study was approved by the CCHMC IRB.
Obesity Measures
BMI was calculated as weight(kg)/height2(m2) and was converted into age and gender specific BMI percentiles34. Conicity index was calculated as [waist circumference(m)/0.109*square root(weight(kg)/height(m)]28. Waist to height ratio was calculated as waist circumference(cm)/ height(cm). Spearman correlation coefficients (r) were used to examine the relationships between BMI percentiles and the other obesity measures. To facilitate the comparison of the obesity measures, the alternative measures were standardized by subtracting the mean and dividing by the standard deviation. All the measures were categorized into three groups based on the 25th and 85th percentile. Participants who were ≤25th percentile of the obesity measure were assigned to the normal, >25th−<85th percentile to the intermediate, and ≥85th percentile to the high weight stratum. Since the 95th percentile gave similar trends to the 85th percentile, the 85th percentile was used as the cutoff for the high weight stratum to allow sufficient analytic power. The 85th percentile is a reasonable cutoff as previous studies have demonstrated that the 85th percentile for BMI provided a sensitivity of 67% in males and 75% in females for total body fat screening35.
Statistical Analysis
When no association was seen between the obesity measures with having asthma in the whole population (n=1123), the analytic population was restricted to children with allergic rhinitis (n=584). Allergic rhinitis was chosen as the control group because a large proportion of asthmatics were skin test positive with allergic rhinitis. Among children with allergic rhinitis, the effect of the obesity measures on the probability of mild asthma vs. no asthma and moderate/severe asthma vs. no asthma was tested. Since the model parameters and odds ratios were similar using both outcomes, the outcome was combined into one three-level asthma severity variable (no asthma, mild asthma, moderate/severe asthma). Generalized logistic regression models were used to investigate the relationship of the obesity measures with asthma severity in children with allergic rhinitis. Logistic regression was used to investigate the relationship between the obesity measures and the likelihood of having at least one positive SPT versus a negative SPT. Skin prick test results were also converted into an atopy index (0, negative to all aeroallergens; 1, positive to 1–2 aeroallergens; 2, positive to 3–4 aeroallergens; or 3, positive to ≥5 aeroallergens) in order to examine the effect of obesity on an incremental increase in allergic sensitization. Proportional odds regression was used to determine the association between each obesity measure and the atopy index. The models were tested in the whole population and then stratified by diagnosis (asthma vs. no asthma).
Continuous variables were logarithmically transformed if needed to achieve normality. In all models, potential covariates considered include race, age group, gender, maternal and paternal education, smoking in the household, and annual household income. Comparisons of categorical data were performed using the chi square test or Fisher’s exact test. The Wilcoxon two-sample test with t-approximation was used to compare continuous data that was not normally distributed. A two-tailed p value ≤ 0.05 was considered statistically significant.
Percentile Curves for Obesity Measures
Percentile curves were constructed for each obesity measure using quantile regression36 for children with allergic rhinitis. Fitted values were computed for the 10th, 25th, 50th, 75th, 85th, 90th, and 95th percentiles. The resulting fitted values, together with the original raw data, were then plotted against age to create the percentile curves separately constructed by race (African American and Caucasian) and gender. BMI percentiles were constructed for Caucasian children ages 5–15 years. The curves for African Americans and for the remainder of the obesity measures were limited to 5–12 year old children due to the sparsity of the data outside this age range. Due to lack of adequate sample size, the 90th percentile of waist circumference for Caucasian girls, and the 95th percentile for the African American girls could not be accurately calculated. The percentile curves for (a) Caucasian boys, (b) Caucasian girls, (c) African American boys, and (d) African American girls are illustrated in Online Repository Figures 1–4 (BMI percentiles, waist circumference, waist to height ratio, and conicity index respectively). In addition, the 25th, 75th, 85th, and 95th percentile distributions of each obesity measure are presented by age and gender in Caucasians (Table Ia online repository) and African Americans (Table Ib, online repository). All the above analyses were conducted using SAS version 9.1.2 (SAS Institute, Cary, NC, USA).
Structural Equation Modeling
In order to account for the mediating effects of the obesity measures in the context of asthma and allergic sensitization, a structural equation model was developed using the Mplus software 37. This model was tested in the whole population (n=1123). A value for the [estimated coefficient/standard error of the estimate] ≥ 1.65 was considered statistically significant (equivalent to the 0.1 level). Further detail of the structural equation modeling is available in the on-line repository.
RESULTS
Characteristics of study subjects
The total study population consisted of 1123 children, ages 5–18 years, and just over half (n=584) of the children were diagnosed with allergic rhinitis (Table I). Of the children with allergic rhinitis, 54.79% had asthma (cases) and 45.21% did not have asthma (controls). No statistical differences in gender, parental education, household member smoking, or annual household income were found between the cases and controls. There were significantly more African Americans in the asthma group (43.13%) versus the control group (34.09%) (p<0.05). Cases were older than the controls, with 60.31% of the cases being 9.5 years and older, compared to 47.73% of the controls (p<0.05). No differences were found in the median and interquartile ranges of the obesity measures between allergic rhinitis children with or without asthma (not shown).
Table I.
Parameter | Total population n=1123 |
All children with allergic rhinitis n=584 |
Group 1: Children with allergic rhinitis and asthma n=320 |
Group 2: Children with allergic rhinitis only (no asthma) n=264 |
||||
---|---|---|---|---|---|---|---|---|
Diagnosis | n | (%) | n | (%) | n | (%) | n | (%) |
Allergic rhinitis | 584 | (52.0) | 584 | (100.0) | 320 | (100.0) | 264 | (100.0) |
Asthma | 469 | (41.76) | 320 | (54.79) | 320 | (100.0) | 0 | 0 |
Age groups* | ||||||||
5 – < 9.5 years | 562 | (50.04) | 265 | (45.38) | 127 | (39.69) | 138 | (52.27) |
9.5 – ≤ 18 years | 561 | (49.96) | 319 | (54.62) | 193 | (60.31) | 126 | (47.73) |
Race* | ||||||||
Caucasian | 645 | (57.44) | 300 | (51.37) | 157 | (49.06) | 143 | (54.17) |
African American | 379 | (33.75) | 228 | (39.04) | 138 | (43.13) | 90 | (34.09) |
Other | 99 | (8.82) | 56 | (9.59) | 25 | (7.81) | 31 | (11.74) |
Males | 620 | (55.21) | 334 | (57.19) | 192 | (60.0) | 142 | (53.79) |
Father’s education | ||||||||
Less than high school | 66 | (5.88) | 34 | (5.82) | 19 | (5.94) | 15 | (5.68) |
High school/some college | 477 | (42.48) | 255 | (43.66) | 133 | (41.56) | 122 | (46.21) |
College or higher | 250 | (22.26) | 113 | (19.35) | 62 | (19.38) | 51 | (19.32) |
Unknown | 330 | (29.38) | 182 | 31.16 | 106 | (33.12) | 76 | (28.79) |
Mother’s education | ||||||||
Less than high school | 49 | (4.36) | 24 | (4.11) | 13 | (4.06) | 11 | (4.17) |
High school/some college | 585 | (52.1) | 309 | (52.91) | 171 | (53.44) | 138 | (52.27) |
College or higher | 263 | (23.42) | 122 | (20.89) | 59 | (18.44) | 63 | (23.86) |
Unknown | 226 | (20.12) | 129 | 22.09 | 77 | (24.06) | 52 | (19.69) |
Annual household income | ||||||||
< $10,000 | 157 | (13.98) | 90 | (15.41) | 49 | (15.31) | 41 | (15.53) |
$10,000–$29,999 | 216 | (19.23) | 116 | (19.86) | 65 | (20.31) | 51 | (19.32) |
$30,000–$49,999 | 133 | (11.84) | 70 | (11.99) | 39 | (12.19) | 31 | (11.74) |
$50,000–$69,999 | 105 | (9.35) | 49 | (8.39) | 19 | (5.94) | 30 | (11.36) |
≥ $70,000 | 235 | (20.93) | 106 | (18.15) | 60 | (18.75) | 46 | (17.42) |
Unknown | 277 | (24.67) | 153 | (26.2) | 88 | (27.50) | 65 | (24.62) |
At least one household member smokes (parental report) | ||||||||
279 | (24.84) | 163 | (27.91) | 89 | (27.81) | 74 | (28.03) |
p < 0.05 between Group 1 and Group 2
BMI percentiles classify 17–46% of obese children differently than the central obesity measures
BMI percentiles showed the strongest correlation with waist to height ratio (r= 0.73) and waist circumference (r=0.59); and the lowest correlation with conicity index (r=0.36). All correlations were statistically significant (p < 0.005) and did not differ by diagnosis (not shown). A comparison of the alternative measures with BMI percentiles using the chi square test is shown in Table II. Among individuals classified as obese using waist circumference, 1.43% were classified as normal weight and 37.14% as intermediate weight using BMI percentiles. Thus, a total of 38.57% (1.43% + 37.14%) of children designated as obese using waist circumference were classified as non-obese using BMI percentiles (discordant). Among those classified as obese using waist to height ratio, 17.19% were discordant using BMI percentiles; using conicity index, 46.27% were discordant using BMI percentiles. All comparisons were significant at the 0.0001 level. Thus, BMI percentiles may classify up to 46% of children differently than the other measures in terms of obesity.
Table II.
Obesity measures | BMI percentile (%) |
P value |
|||||
---|---|---|---|---|---|---|---|
≤ 25% | > 25% – < 85% | ≥ 85% | |||||
Waist circumference (cm) | n | (%) | n | (%) | n | (%) | |
≤ 25% | 49 | (43.75) | 61 | (54.46) | 2 | (1.79) | <0.0001 |
> 25% – < 85% | 51 | (17.0) | 223 | (74.33) | 26 | (8.67) | |
≥ 85% | 1 | (1.43) | 26 | (37.14) | 43 | (61.43) | |
Waist to height ratio | |||||||
≤ 25% | 63 | (52.94) | 54 | (45.38) | 2 | (1.68) | <0.0001 |
> 25% – < 85% | 37 | (12.37) | 246 | (82.27) | 16 | (5.35) | |
≥ 85% | 1 | (1.56) | 10 | (15.63) | 53 | (82.81) | |
Conicity index (m/√(kg/m)) | |||||||
≤ 25% | 28 | (23.73) | 83 | (70.34) | 7 | (5.93) | <0.0001 |
>25% – < 85% | 69 | (23.23) | 200 | (67.34) | 28 | (9.43) | |
≥ 85% | 4 | (5.97) | 27 | (40.30) | 36 | (53.73) |
Prevalence of moderate/severe asthma is higher in centrally obese children with allergic rhinitis
Generalized logistic regression models with the cumulative logit function were used to determine the effect of each obesity measure on the likelihood of having asthma compared with no asthma among children with allergic rhinitis. The models were adjusted for age and race. Gender did not differ between the groups, but it was still included in the models. As shown in Table III, the proportion of children with moderate/severe asthma was significantly higher among children who were in the high conicity index stratum (≥85%). This trend reached significance only with the measure of conicity index, but trended toward significant for the other measures of central obesity. Across conicity index strata, the proportion of children with moderate/severe asthma steadily increased from 28.57% to 36.88% to 43.75% (p<0.01). Children classified as obese using the conicity index were approximately 2.6 times more likely to have asthma (OR=2.63, 95% CI=1.19–5.82) (p<0.05). These trends were maintained in Caucasians. The associations could not be assessed in African Americans due to the limited sample size.
Table III.
Obesity measures | No asthma | Mild asthma |
Moderate/Severe asthma |
Unadjusted OR (95% CI) |
Adjusted OR* (95% CI) |
|||
---|---|---|---|---|---|---|---|---|
BMI percentiles (%) | n | (%) | n | (%) | n | (%) | ||
≤ 25% | 45 | (38.79) | 27 | (23.28) | 44 | (37.93) | Reference | Reference |
>25% – < 85% | 110 | (32.54) | 99 | (29.29) | 129 | (38.17) | 1.15 (0.78–1.71) | 0.92 (0.60–1.41) |
≥ 85% | 21 | (24.42) | 30 | (34.88) | 35 | (40.69) | 1.43 (0.86–2.39) | 1.03 (0.59–1.79) |
Waist circumference (cm) | ||||||||
≤ 25% | 27 | (47.37) | 13 | (22.81) | 17 | (29.82) | Reference | Reference |
>25% – < 85% | 54 | (31.58) | 50 | (29.24) | 67 | (39.18) | 1.78 (1.01–3.15)† | 1.40 (0.69–2.82) |
≥ 85% | 12 | (27.27) | 18 | (40.91) | 14 | (31.82) | 1.65 (0.80–3.39) | 1.20 (0.49–2.92) |
Waist to height ratio | ||||||||
≤ 25% | 21 | (31.82) | 23 | (34.85) | 22 | (33.33) | Reference | Reference |
>25% – < 85% | 64 | (39.51) | 43 | (26.54) | 55 | (33.95) | 0.85 (0.51–1.44) | 0.93 (0.54–1.60) |
≥ 85% | 5 | (14.71) | 13 | (38.23) | 16 | (47.06) | 1.91 (0.89–4.04) | 2.00 (0.93–4.31) |
Conicity index (m/√(kg/m)) | ||||||||
≤ 25% | 23 | (32.86) | 27 | (38.57) | 20 | (28.57) | Reference | Reference |
>25% – < 85% | 64 | (40.0) | 37 | (23.12) | 59 | (36.88) | 1.02 (0.61–1.69) | 1.16 (0.67–2.01) |
≥ 85% | 3 | (9.38) | 15 | (46.88) | 14 | (43.75) | 2.15 (1.02–4.53) † | 2.63 (1.19–5.82)† |
Regression analysis was used to model the effect of each obesity measure on the likelihood of mild or moderate/severe asthma compared to allergic rhinitis without asthma.
Adjusted for age group, race and gender.
p<0.05
The effect of each obesity measure on FEV1 was examined. (Table IV). BMI percentiles were significantly associated with FEV1 both in children with (β coefficient=0.24) and without (β coefficient=0.53) allergic rhinitis, albeit more strongly in those without allergic rhinitis (p<0.01). Waist circumference was associated with a lower mean FEV1 (p<0.05). The obesity measures explained 8% - 24% of the variance in the FEV1 in children with allergic rhinitis, and 2% - 31% of the variance in children without allergic rhinitis. Notably, in children without allergic rhinitis, BMI percentiles explained the most variance in FEV1 (R2=0.31) while the conicity index explained the least (R2=0.02). In contrast, in children with allergic rhinitis, waist to height ratio explained the most variance in FEV1 (R2=0.24) while BMI percentiles explained the least (R2=0.08).
Table IV.
Obesity measures | Allergic rhinitis | No allergic rhinitis | ||||||
---|---|---|---|---|---|---|---|---|
n | Standardized β coefficient |
Model R2 | P value | n | Standardized β coefficient |
Model R2 | P value | |
BMI percentiles (kg/m2) | 139 | 0.24 | 0.08 | 0.005 | 46 | 0.53 | 0.31 | 0.0005 |
Waist circumference (cm) | 56 | 0.19 | 0.15 | 0.17 | 27 | 0.51 | 0.19 | 0.04 |
Waist to height ratio | 51 | 0.29 | 0.24 | 0.04 | 26 | 0.36 | 0.13 | 0.11 |
Conicity index (m/√(kg/m)) | 51 | 0.23 | 0.20 | 0.12 | 26 | −0.03 | 0.02 | 0.91 |
Adjusted for race, age group, gender, and income.
Association of obesity with the prevalence of allergic sensitization
Logistic regression was used to investigate the relationship between the obesity measures and the likelihood of having at least one positive SPT versus a negative SPT in the total population stratified by asthma diagnosis (Table V). The proportional odds model was also used to obtain ORs for the association of each obesity measure with the atopy index. Among the potential covariates, age and gender were significantly associated with the atopy index, thus age and gender were included in the multivariable regression models, in addition to parental education. The presence of obesity was inversely correlated with an increasing atopy index among children with asthma for both BMI percentiles (OR=0.49, 95% CI=0.27–0.90) and waist circumference (OR=0.38, 95% CI=0.14–1.01) (p<0.05).
Table V.
Obesity measure | Current asthma | No current asthma | ||||||
---|---|---|---|---|---|---|---|---|
n | (%) | Unadjusted OR (95% CI) |
Adjusted * OR (95% CI) |
n | (%) | Unadjusted OR (95% CI) |
Adjusted OR (95% CI) |
|
BMI percentiles (%) | ||||||||
≤25% | 88 | (21.84) | Reference | Reference | 60 | (22.06) | Reference | Reference |
>25% – <85% | 251 | (62.28) | 0.69 (0.44–1.08) |
0.69 (0.44–1.09) |
168 | (61.76) | 1.06 (0.63–1.79) |
1.12 (0.65–1.92) |
≥85% | 64 | (15.88) | 0.50 (0.28–0.89)* |
0.49 (0.27–0.90)* |
44 | (16.18) | 0.66 (0.32–1.34) |
0.77 (0.36–1.67) |
Waist circumference (cm) | ||||||||
≤25% | 46 | (23.71) | Reference | Reference | 33 | (20.89) | Reference | Reference |
>25% – <85% | 112 | (57.73) | 0.85 (0.49–1.48) |
0.59 (0.29–1.19) |
105 | (66.46) | 0.90 (0.48–1.71) |
1.04 (0.48–2.24) |
≥85% | 36 | (18.56) | 0.63 (0.31–1.27) |
0.38 (0.14–1.01)* |
20 | (12.66) | 0.91 (0.35–2.34) |
1.19 (0.36–3.94) |
Waist to height ratio | ||||||||
≤25% | 47 | (25.68) | Reference | Reference | 34 | (21.79) | Reference | Reference |
>25% – <85% | 106 | (57.92) | 0.89 (0.52–1.56) |
1.13 (0.59–2.16) |
105 | (67.31) | 2.54 (1.28–5.03) |
2.48 (1.16–5.27)* |
≥85% | 30 | (16.39) | 0.60 (0.29–1.25) |
0.72 (0.30–1.73) |
17 | (10.90) | 2.87 (1.06–7.81)* |
2.38 (0.76–7.46) |
Conicity index (m/√(kg/m)) |
||||||||
≤25% | 49 | (26.78) | Reference | Reference | 37 | (23.72) | Reference | Reference |
>25% – <85% | 102 | (55.74) | 0.96 (0.55–1.68) |
1.06 (0.56–2.00) |
103 | (66.03) | 1.76 0.93–3.35) |
1.95 (0.94–4.05) |
≥85% | 32 | (17.49) | 0.62 (0.30–1.25) |
0.69 (0.29–1.66) |
16 | (10.26) | 2.05 (0.78–5.37) |
1.75 (0.57–5.38) |
p ≤ 0.05
Adjusted for age group, gender, and parental education
The structural equation model confirms the association of central obesity with asthma
A structural equation model was utilized to assess the mediating effects of the obesity measures on asthma in the total population. The obesity measures were sequentially removed using backward elimination, starting with BMI percentiles. After removing BMI percentiles, the model fit improved significantly and no further elimination steps were needed. Figure 5 (Online Repository) displays the full structural equation model with the significant predictors and pathways shown in bold. Asthma was significantly associated with the measures of central obesity (Table VI). For each unit increase in waist circumference, the OR for asthma was significantly increased by about 3-fold (OR=2.95). Similarly, waist to height ratio in boys was positively associated with asthma (OR=2.43). In girls, conicity index was negatively associated with asthma (OR=0.43). None of the obesity measures were associated with the atopy index (data not shown).
Table VI.
Parameter | Outcome=Asthma | |
---|---|---|
OR | [estimated coefficient/standard error of the estimate] | |
Race | ||
Caucasian | 0.94 | −0.26 |
African American | 1.56 | 1.90 |
Other | Reference | |
Age (yrs) | 0.89 | −2.95 |
Pets in the home | ||
Cat | 0.98 | −0.12 |
Dog | 0.89 | −0.73 |
Cat and dog | 0.80 | −1.12 |
Other pets | Reference | |
Gender | ||
Male | 1.32 | 2.23 |
Female | Reference | |
Obesity measures | ||
Waist circumference (cm) | 2.95 | 3.55 |
Waist to height ratio | 0.69 | −1.13* |
Conicity index (m/√(kg/m)) | 0.73 | −1.39‡ |
Atopy index | 0.98 | −0.31 |
Males (OR=2.43; [estimated coefficient/standard error of the estimate]=2.07)
Females (OR=0.43; [estimated coefficient/standard error of the estimate]= −2.88)
DISCUSSION
Central obesity is the most critical determinant of obesity-related morbidity in many diseases. However, studies directly comparing obesity measures that assess central obesity with BMI measures are lacking in childhood asthma and allergic rhinitis. We directly compared obesity measures in children with allergic rhinitis with or without asthma. Our results demonstrate that measures that account for fat distribution and central obesity classify obesity differently than BMI. In fact, there was up to 46% discordance between BMI percentiles and the central obesity measures. Thus, a significant proportion of children with allergic rhinitis designated as obese or non-obese using BMI percentiles will be designated differently using alternative measures that account for central obesity. Furthermore, we observed a significant association of central obesity (assessed using conicity index) with having asthma and with more severe asthma. Although BMI percentiles were associated with asthma and asthma severity in Caucasians, the associations of central obesity measures with asthma were more consistent (even in mixed populations and in Caucasians), suggesting that central obesity may be superior to BMI percentiles in assessing the likelihood for having asthma in children with allergic rhinitis.
In contrast to asthma severity, a negative association was observed between obesity and allergic sensitization among asthmatics. Thus, allergic sensitization was less common among the obese subgroup. This finding was more pronounced with central obesity (assessed using waist circumference), and is supported by a study that found that central obesity was associated with non-atopic asthma in adults38. This suggests that among obese children, there are factors that contribute to the development of asthma independent of allergic sensitization. This is an important and intriguing observation. Allergic sensitization still occurs in the context of obesity, but mechanisms other than allergic sensitization likely contribute to the link between obesity and asthma. The structural equation model further supported this observation, since none of the obesity measures were associated with atopy, despite the robust association of central obesity with asthma.
To date, the majority of the studies that support an association between asthma and obesity using measures that assess fat distribution have been performed in adults and have been mainly limited to Caucasians7, 38–40. The study herein has several advantages. First, it was performed in Caucasian and African American children. In addition, the racial and socioeconomic makeup of the children participating in this study is similar to the national census figures (year 2000 figures, www.censusscope.org). The only exception is a higher proportion of African Americans, which is not surprising since asthma disproportionately affects this subgroup. Second, weight and height were objectively measured. In previous studies that found an association between obesity with asthma, several used self-reported weight and height41, 42, which is a potential source of error due to reporting bias. Third, the diagnosis of asthma was based on objective lung function criteria, while other studies have relied largely on self-reported asthma18, 41, 43. Fourth, percentile curves were constructed for each obesity measure, providing race and gender-specific quantile reference values for this specific population. Finally, a structural equation model, examining the indirect effects of the obesity measures, confirmed the association of central obesity with asthma in all the children.
This study is not generalizable to the US population because it was performed in a clinic sample of children. Although the relationship between asthma and obesity, and specifically central obesity, is supported by our findings, no conclusions about causality can be made due to the cross-sectional design. Potential confounders that may impact the association between asthma and obesity include gastro-esophageal reflux disease and sleep disordered breathing. Neither of these was assessed in this study. However, gastro-esophageal reflux disease did not have an effect on the association between asthma and obesity in a longitudinal study49. Similarly, sleep disordered breathing based on sleep apnea or habitual snoring did not alter the association between obesity and asthma50.
Given the burden of childhood obesity, these results have public health relevance. Based on these data, measures of central obesity should be incorporated in pediatric and allergy/immunology practices in order to better identify patients with allergic rhinitis who may be at increased risk for asthma due to co-morbid obesity.
Supplementary Material
Acknowledgements
This work was supported by NIH U19A170235-01 (G.K.H.) and University of Cincinnati, Molecular Epidemiology in Children’s Environmental Health - Institutional NIEHS T32 ES10957 (S.M.)
We gratefully acknowledge the help and support of the Allergy and Immunology Clinic nurses, physicians, fellows and staff, as well as the families and children who participated in this study.
Abbreviations
- BMI
body mass index
- FEV1
forced expiratory volume in one second
- SPT
skin prick test
Footnotes
Disclosures: No financial relationships to disclose.
Capsule summary: Measures of central obesity, including waist to height ratio and conicity index, may improve the evaluation of asthma susceptibility and severity in children with allergic rhinitis when compared to standard BMI measures.
References
- 1.Ogden CL, Carroll MD, Curtin LR, McDowell MA, Tabak CJ, Flegal KM. Prevalence of overweight and obesity in the united states, 1999–2004. JAMA. 2006 Apr 5;295(13):1549–1555. doi: 10.1001/jama.295.13.1549. [DOI] [PubMed] [Google Scholar]
- 2.Mannino DM, Homa D, Akinbami LJ, Moorman JE, Gwynn C, Redd S. Surveillance for asthma-United States, 1980–1999. Morbidity and Mortality Weekly Report, Centers for Disease Control and Prevention (CDC) 2002:1–13. Report No.: 51(SS01) [PubMed] [Google Scholar]
- 3.Tantisira KG, Weiss ST. Complex interactions in complex traits: Obesity and asthma. Thorax. 2001 Sep 56; Suppl 2:64–73. [PMC free article] [PubMed] [Google Scholar]
- 4.Boulet LP, Hamid Q, Bacon SL, Bergeron C, Boulet LP, Chen Y, et al. Symposium on obesity and asthma - November 2, 2006. Can Respir J. 2007 May-Jun 14;(4):201–208. doi: 10.1155/2007/342618. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Ford ES, Mannino DM. Time trends in obesity among adults with asthma in the United States: Findings from three national surveys. J Asthma. 2005 Mar;42(2):91–95. [PubMed] [Google Scholar]
- 6.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 Nov 15;160(10):969–976. doi: 10.1093/aje/kwh303. [DOI] [PubMed] [Google Scholar]
- 7.Kronander UN, Falkenberg M, Zetterstrom O. Prevalence and incidence of asthma related to waist circumference and BMI in a Swedish community sample. Respir Med. 2004 Nov;98(11):1108–1116. doi: 10.1016/j.rmed.2004.03.022. [DOI] [PubMed] [Google Scholar]
- 8.Bibi H, Shoseyov D, Feigenbaum D, Genis M, Friger M, Peled R, et al. The relationship between asthma and obesity in children: Is it real or a case of over diagnosis? J Asthma. 2004 Jun;41(4):403–410. doi: 10.1081/jas-120026097. [DOI] [PubMed] [Google Scholar]
- 9.Ronmark E, Andersson C, Nystrom L, Forsberg B, Jarvholm B, Lundback B. Obesity increases the risk of incident asthma among adults. Eur Respir J. 2005 Feb;25(2):282–288. doi: 10.1183/09031936.05.00054304. [DOI] [PubMed] [Google Scholar]
- 10.Beuther DA, Sutherland ER. Overweight, obesity, and incident asthma: A meta-analysis of prospective epidemiologic studies. Am J Respir Crit Care Med. 2007 Apr 1;175(7):661–666. doi: 10.1164/rccm.200611-1717OC. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Aaron SD, Fergusson D, Dent R, Chen Y, Vandemheen KL, Dales RE. Effect of weight reduction on respiratory function and airway reactivity in obese women. Chest. 2004 Jun;125(6):2046–2052. doi: 10.1378/chest.125.6.2046. [DOI] [PubMed] [Google Scholar]
- 12.Gold DR, Damokosh AI, Dockery DW, Berkey CS. Body-mass index as a predictor of incident asthma in a prospective cohort of children. Pediatr Pulmonol. 2003 Dec;36(6):514–521. doi: 10.1002/ppul.10376. [DOI] [PubMed] [Google Scholar]
- 13.Oddy WH, Sherriff JL, de Klerk NH, Kendall GE, Sly PD, Beilin LJ, et al. The relation of breastfeeding and body mass index to asthma and atopy in children: A prospective cohort study to age 6 years. Am J Public Health. 2004 Sep;94(9):1531–1537. doi: 10.2105/ajph.94.9.1531. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Tsai HJ, Tsai AC, Nriagu J, Ghosh D, Gong M, Sandretto A. Associations of BMI, TV-watching time, and physical activity on respiratory symptoms and asthma in 5th grade schoolchildren in Taipei, Taiwan. J Asthma. 2007 Jun;44(5):397–401. doi: 10.1080/02770900701364304. [DOI] [PubMed] [Google Scholar]
- 15.Mannino DM, Mott J, Ferdinands JM, Camargo CA, Friedman M, Greves HM, et al. Boys with high body masses have an increased risk of developing asthma: Findings from the National Longitudinal Survey of Youth (NLSY) Int J Obes (Lond) 2006 Jan;30(1):6–13. doi: 10.1038/sj.ijo.0803145. [DOI] [PubMed] [Google Scholar]
- 16.Castro-Rodriguez JA, Holberg CJ, Morgan WJ, Wright AL, Martinez FD. Increased incidence of asthma like symptoms in girls who become overweight or obese during the school years. Am J Respir Crit Care Med. 2001 May;163(6):1344–1349. doi: 10.1164/ajrccm.163.6.2006140. [DOI] [PubMed] [Google Scholar]
- 17.Cassol V, Rizzato TM, Teche SP, Basso DF, Centenaro DF, Maldonado M, et al. Obesity and its relationship with asthma prevalence and severity in adolescents from southern Brazil. J Asthma. 2006 Feb;43(1):57–60. doi: 10.1080/02770900500448597. [DOI] [PubMed] [Google Scholar]
- 18.Wickens K, Barry D, Friezema A, Rhodius R, Bone N, Purdie G, et al. Obesity and asthma in 11–12 year old New Zealand children in 1989 and 2000. Thorax. 2005 Jan;60(1):7–12. doi: 10.1136/thx.2002.001529. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.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 Mar;42(2):97–99. doi: 10.1081/jas-51338. [DOI] [PubMed] [Google Scholar]
- 20.Hasler G, Gergen PJ, Ajdacic V, Gamma A, Eich D, Rossler W, et al. Asthma and body weight change: A 20-year prospective community study of young adults. Int J Obes (Lond) 2006 Jul;30(7):1111–1118. doi: 10.1038/sj.ijo.0803215. [DOI] [PubMed] [Google Scholar]
- 21.Daniels SR, Khoury PR, Morrison JA. The utility of body mass index as a measure of body fatness in children and adolescents: Differences by race and gender. Pediatrics. 1997 Jun;99(6):804–807. doi: 10.1542/peds.99.6.804. [DOI] [PubMed] [Google Scholar]
- 22.Wang Y. Epidemiology of childhood obesity--methodological aspects and guidelines: What is new? Int J Obes Relat Metab Disord. 2004 Nov;28 Suppl 3:S21–S28. doi: 10.1038/sj.ijo.0802801. [DOI] [PubMed] [Google Scholar]
- 23.Moreno LA, Fleta J, Sarria A, Rodriguez G, Gil C, Bueno M. Secular changes in body fat patterning in children and adolescents of Zaragoza (Spain), 1980–1995. Int J Obes Relat Metab Disord. 2001 Nov;25(11):1656–1660. doi: 10.1038/sj.ijo.0801803. [DOI] [PubMed] [Google Scholar]
- 24.Ashwell M, Hsieh SD. Six reasons why the waist-to-height ratio is a rapid and effective global indicator for health risks of obesity and how its use could simplify the international public health message on obesity. Int J Food Sci Nutr. 2005 Aug;56(5):303–307. doi: 10.1080/09637480500195066. [DOI] [PubMed] [Google Scholar]
- 25.Lofgren I, Herron K, Zern T, West K, Patalay M, Shachter NS, et al. Waist circumference is a better predictor than body mass index of coronary heart disease risk in overweight premenopausal women. J Nutr. 2004 May;134(5):1071–1076. doi: 10.1093/jn/134.5.1071. [DOI] [PubMed] [Google Scholar]
- 26.Kahn HS, Imperatore G, Cheng YJ. A population-based comparison of BMI percentiles and waist-to-height ratio for identifying cardiovascular risk in youth. J Pediatr. 2005 Apr;146(4):482–488. doi: 10.1016/j.jpeds.2004.12.028. [DOI] [PubMed] [Google Scholar]
- 27.Valdez R. A simple model-based index of abdominal adiposity. J Clin Epidemiol. 1991;44(9):955–956. doi: 10.1016/0895-4356(91)90059-i. [DOI] [PubMed] [Google Scholar]
- 28.Valdez R, Seidell JC, Ahn YI, Weiss KM. A new index of abdominal adiposity as an indicator of risk for cardiovascular disease. A cross-population study. Int J Obes Relat Metab Disord. 1993 Feb;17(2):77–82. [PubMed] [Google Scholar]
- 29.Worldwide variation in prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and atopic eczema: ISAAC. The International Study of Asthma and Allergies in Childhood (ISAAC) steering committee. Lancet. 1998 Apr 25;351(9111):1225–1232. [PubMed] [Google Scholar]
- 30.Asher MI, Keil U, Anderson HR, Beasley R, Crane J, Martinez F, et al. International Study of Asthma and Allergies in Childhood (ISAAC): Rationale and methods. Eur Respir J. 1995 Mar;8(3):483–491. doi: 10.1183/09031936.95.08030483. [DOI] [PubMed] [Google Scholar]
- 31.National Heart, Lung, and Blood Institute. NAEPP, expert panel report 3, guidelines for the diagnosis and management of asthma, NIH publication number 08-5846. 2007 [Google Scholar]
- 32.U.S. Department of Health and Human Services, Centers for Disease Control and Prevention. Anthropometry and physical activity monitor procedures manual. 2005 [Google Scholar]
- 33.Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, et al. Standardisation of spirometry. Eur Respir J. 2005 Aug;26(2):319–338. doi: 10.1183/09031936.05.00034805. [DOI] [PubMed] [Google Scholar]
- 34.A SAS program for the CDC growth charts. 2005 [ http://www.cdc.gov/nccdphp/dnpa/growthcharts/resources/sas.htm].
- 35.Lazarus R, Baur L, Webb K, Blyth F. Body mass index in screening for adiposity in children and adolescents: Systematic evaluation using receiver operating characteristic curves. Am J Clin Nutr. 1996 Apr;63(4):500–506. doi: 10.1093/ajcn/63.4.500. [DOI] [PubMed] [Google Scholar]
- 36.Koenker R, Bassett G., Jr Regression quantiles. Econometrica. 1978;46(1):33–50. [Google Scholar]
- 37.Muthen LK, Muthen BO. Mplus user’s guide. Fourth ed. Los Angeles, CA: Muthen & Muthen; 1998–2006. [Google Scholar]
- 38.Appleton SL, Adams RJ, Wilson DH, Taylor AW, Ruffin RE. North West Adelaide Health Study Team. Central obesity is associated with nonatopic but not atopic asthma in a representative population sample. J Allergy Clin Immunol. 2006 Dec;118(6):1284–1291. doi: 10.1016/j.jaci.2006.08.011. [DOI] [PubMed] [Google Scholar]
- 39.Chen Y, Rennie D, Cormier Y, Dosman J. Sex specificity of asthma associated with objectively measured body mass index and waist circumference. The Humboldt study. Chest. 2005 Oct;128(4):3048–3054. doi: 10.1378/chest.128.4.3048. [DOI] [PubMed] [Google Scholar]
- 40.Del-Rio-Navarro BE, Fanghanel G, Berber A, Sanchez-Reyes L, Estrada-Reyes E, Sienra-Monge JJ. The relationship between asthma symptoms and anthropometric markers of overweight in a Hispanic population. J Investig Allergol Clin Immunol. 2003;13(2):118–123. [PubMed] [Google Scholar]
- 41.Kilpelainen M, Terho EO, Helenius H, Koskenvuo M. Body mass index and physical activity in relation to asthma and atopic diseases in young adults. Respir Med. 2006 Sep;100(9):1518–1525. doi: 10.1016/j.rmed.2006.01.011. [DOI] [PubMed] [Google Scholar]
- 42.Luder E, Ehrlich RI, Lou WY, Melnik TA, Kattan M. Body mass index and the risk of asthma in adults. Respir Med. 2004 Jan;98(1):29–37. doi: 10.1016/j.rmed.2003.08.004. [DOI] [PubMed] [Google Scholar]
- 43.Ford ES, Mannino DM, Redd SC, Mokdad AH, Mott JA. Body mass index and asthma incidence among USA adults. Eur Respir J. 2004 Nov;24(5):740–744. doi: 10.1183/09031936.04.00088003. [DOI] [PubMed] [Google Scholar]
- 44.Harle P, Straub RH. Leptin is a link between adipose tissue and inflammation. Ann N Y Acad Sci. 2006 Jun;1069:454–462. doi: 10.1196/annals.1351.044. [DOI] [PubMed] [Google Scholar]
- 45.Matarese G, Moschos S, Mantzoros CS. Leptin in immunology. J Immunol. 2005 Mar 15;174(6):3137–3142. doi: 10.4049/jimmunol.174.6.3137. [DOI] [PubMed] [Google Scholar]
- 46.Shum BO, Mackay CR, Gorgun CZ, Frost MJ, Kumar RK, Hotamisligil GS, et al. The adipocyte fatty acid-binding protein aP2 is required in allergic airway inflammation. J Clin Invest. 2006 Aug;116(8):2183–2192. doi: 10.1172/JCI24767. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Parameswaran K, Todd DC, Soth M. Altered respiratory physiology in obesity. Can Respir J. 2006 May-Jun;13(4):203–210. doi: 10.1155/2006/834786. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.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 Dec 1;164(11):2045–2050. doi: 10.1164/ajrccm.164.11.2004235. [DOI] [PubMed] [Google Scholar]
- 49.Gunnbjornsdottir MI, Omenaas E, Gislason T, Norrman E, Olin AC, Jogi R, et al. Obesity and nocturnal gastro-oesophageal reflux are related to onset of asthma and respiratory symptoms. Eur Respir J. 2004 Jul;24(1):116–121. doi: 10.1183/09031936.04.00042603. [DOI] [PubMed] [Google Scholar]
- 50.Sulit LG, Storfer-Isser A, Rosen CL, Kirchner HL, Redline S. Associations of obesity, sleep-disordered breathing, and wheezing in children. Am J Respir Crit Care Med. 2005 Mar 15;171(6):659–664. doi: 10.1164/rccm.200403-398OC. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.