Supported, in part, by grants from the NIH (T32 DK007634, 5-KL2-RR025746-02, P30 DK034987), and a junior faculty career development award from the Crohn's and Colitis Foundation of America.
Prevalence and epidemiology of overweight and obesity in children with inflammatory bowel disease †
Article first published online: 17 DEC 2010
Copyright © 2010 Crohn's & Colitis Foundation of America, Inc.
Inflammatory Bowel Diseases
Volume 17, Issue 10, pages 2162–2168, October 2011
How to Cite
Long, M. D., Crandall, W. V., Leibowitz, I. H., Duffy, L., del Rosario, F., Kim, S. C., Integlia, M. J., Berman, J., Grunow, J., Colletti, R. B., Schoen, B. T., Patel, A. S., Baron, H., Israel, E., Russell, G., Ali, S., Herfarth, H. H., Martin, C., Kappelman, M. D. and on behalf of the ImproveCareNow Collaborative for Pediatric IBD (2011), Prevalence and epidemiology of overweight and obesity in children with inflammatory bowel disease . Inflamm Bowel Dis, 17: 2162–2168. doi: 10.1002/ibd.21585
- Issue published online: 11 SEP 2011
- Article first published online: 17 DEC 2010
- Manuscript Accepted: 24 OCT 2010
- Manuscript Received: 6 OCT 2010
Obesity is a significant public health threat to children in the United States. The aims were to: 1) Determine the prevalence of obesity in a multicenter cohort of children with inflammatory bowel disease (IBD); 2) Evaluate whether overweight and obese status is associated with patient demographics or disease characteristics.
We used data from the ImproveCareNow Collaborative for pediatric IBD, a multicenter registry of children with IBD, collected between April 2007 and December 2009. Children ages 2–18 years were classified into body mass index (BMI) percentiles. Bivariate analyses and multivariate logistic regression were used to compare demographic and disease characteristics by overweight (BMI >85%) and obese (BMI >95%) status.
The population consisted of 1598 children with IBD. The prevalence of overweight/obese status in pediatric IBD is 23.6%, (20.0% for Crohn's disease [CD] and 30.1% for ulcerative colitis [UC] and indeterminate colitis [IC]). African American race (odds ratio [OR] 1.64, 95% confidence interval [CI] 1.10–2.48) and Medicaid insurance (OR 1.67, 95% CI 1.19–2.34) were positively associated with overweight/obese status. Prior IBD-related surgery (OR 1.73, 95% CI 1.07–2.82) was also associated with overweight and obese status in children with CD. Other disease characteristics were not associated with overweight and obesity in children with IBD.
Approximately one in five children with CD and one in three with UC are overweight or obese. Rates of obesity in UC are comparable to the general population. Obese IBD patients may have a more severe disease course, as indicated by increased need for surgery. Sociodemographic risk factors for obesity in the IBD population are similar to those in the general population. (Inflamm Bowel Dis 2010;)
Across the United States the prevalence of overweight and obese children has dramatically increased over the past decade.1, 2 For the general population of U.S. children ages 2–19 during 2007–2008, 11.9% (95% confidence interval [CI] 9.8%–13.9%) were at or above the 97th percentile, 16.9% (95% CI 14.1%–19.6%) were at or above the 95th percentile, and 31.7% (95% CI 29.2%–34.1%) were at or above the 85th percentile of the body mass index (BMI)-for-age growth charts.3 With this increase in obesity, serious comorbid conditions such as diabetes and hypertension have also increased.4–6 Obese children are at increased risk for staying overweight or obese throughout adulthood.5, 7 In addition to the general risks associated with overweight and obese status, obesity may have disease-specific risks in children with inflammatory bowel disease (IBD). Prior studies in adults with IBD have shown increased morbidity, increased disease activity, and more frequent perianal complications associated with obesity.8 Furthermore, obesity-related comorbidities may also contribute to long-term IBD morbidity and mortality as well as contribute to polypharmacy and possible medication interactions. Little is known about the prevalence and role of overweight and obesity among the subpopulation of children with IBD.
Traditionally, children with IBD have been described as malnourished and underweight. In a previous study of BMI among those with juvenile onset IBD in Great Britain from 1968–1983, BMI was found to be lower than that of the general population.9 However, in a more recent study of North American children with newly diagnosed IBD from 2001–2005, ≈10% of children with Crohn's disease (CD) and 20%–30% of children with ulcerative colitis (UC) had a BMI consistent with overweight or at risk for overweight status at the time of IBD diagnosis.10 Rates of obesity in the treated pediatric IBD population remain unknown. Furthermore, rates of obesity within the general population have changed since this time, and such secular trends may similarly affect children with IBD.
We therefore aimed to determine the prevalence of obesity among a multicenter cohort of children with IBD and to evaluate whether overweight and obese status is associated with patient demographics or disease characteristics.
MATERIALS AND METHODS
We performed a cross-sectional study of children with IBD enrolled in the ImproveCareNow collaborative for pediatric IBD. The collaborative has enrolled and prospectively followed children with previously and newly diagnosed IBD since April 2007. Demographic information was collected at the enrollment visit, and disease characteristics including weight and height, disease phenotype, medications, surgeries, presence of perirectal disease, and physician's global assessment of current disease were recorded at all visits. In this analysis we included all patients between the ages of 2 and 18 years of age who were enrolled at actively participating centers (see Appendix) and had at least two documented visits between April 1, 2007 and December 31, 2009 in which height, weight, and disease-specific factors were measured and recorded. Patients were excluded if there was >10% reduction in height or >20% change in BMI at follow-up visit, as this was felt to represent measurement error.
Determination of Outcome of Overweight and Obesity
Excess weight in children ages 2–19 is defined by BMI in relation to the 2000 Centers for Disease Control and Prevention (CDC) sex-specific BMI-for-age growth charts.11 The most recent expert committee guidelines on childhood obesity have labeled children ages 2–19 years with a >95th BMI percentile as obese and children between the 85th and 95th BMI percentiles as overweight.12 Therefore, for this study we adapted BMI-for-age-percentiles for girls and boys ages 2–18 from the CDC percentile data values. Overweight status and obesity were defined by three levels: at or above the 85th percentile for BMI-for-age (overweight), at or above the 95th percentile (obese), or at or above the 97th percentile (severe obesity). These cutpoints have been used previously in the literature and coincide with expert guidelines.3 BMI cutpoints were analyzed by subcategory and also in a dichotomous fashion: overweight or obese (>85th percentile) versus nonoverweight or obese (≤85th percentile). For all children with results >97th percentile or <3rd percentile, individual sites were contacted to manually confirm height and weight measurements and units. Of the 131 records selected for auditing, only four errors (3%) were identified and corrected. Two charts could not be located. For each child the most recent visit with height and weight data was used to calculate the BMI-for-age percentile.
Determination of Exposures
For each participant, demographic characteristics such as age, self-reported race, and insurance status were recorded. We additionally asked information on self-perceived ethnicity. Clinical characteristics of IBD were also obtained, including disease type (CD, UC, or indeterminate colitis [IC]), disease duration (defined as years from onset of disease to most current visit), disease phenotype (for CD), prior IBD-related surgeries, presence of perianal disease on physical exam, and physician global assessment of disease status (inactive, mild, moderate, or severe). Diagnosis of CD, UC, or IC was made based on all available radiologic, pathologic, and endoscopic information. Disease assessment was performed at each visit, and a diagnosis could be revised to another IBD subtype at subsequent visits. Physician's global assessment has been shown to correlate with both the Pediatric Crohn's Disease Activity Index (PCDAI) and the short PCDAI in the data from this collaborative.13 Immunosuppressive medication use and corticosteroid use was also recorded from the most recent clinic visit where height and weight was assessed in order to determine the effects of particular medications on BMI percentiles.
Bivariate analyses were used to compare patient demographic characteristics and disease factors between overweight and obese children and nonoverweight and obese children with both CD and UC or IC. Prevalence of various categories of BMI-for-age percentiles, including underweight, normal, and overweight ranges of percentiles, in the IBD population by disease subtype were then compared. Multivariate logistic regression modeling was used to identify the independent effects of demographic and disease characteristics on overweight and obese status among children with IBD and by CD or UC/IC subtype. Variables were selected for the models a priori based on the prior literature.
For all analyses P-values were two-sided and a P-value of 0.05 or less was considered statistically significant. All statistical analyses were performed using STATA v. 9.0 (College Station, TX). The study protocol was approved by all sites participating in the collaborative, and informed consent was obtained if required by Institutional Review Boards.
The initial database contained data on 2042 children aged 2–18 years with IBD from actively enrolling sites. Of these, we excluded 417 children due to the lack of at least two separate measurements of height and weight and 46 children with >10% reduction in height, or >20% change in BMI between subsequent visits. One additional child was excluded, as there was no initial diagnosis of CD, UC, or IC. Only 45 patients (2.8% of population) changed IBD subtype at subsequent visits. The final study population included 1598 children.
Table 1 demonstrates the demographic and clinical characteristics of children with CD by overweight or obese status. Those children who were overweight or obese were more likely to be of a non-Caucasian race and to have Medicaid insurance (as a marker for socioeconomic status). Younger age was also statistically associated with overweight and obese status, although the absolute magnitude of this difference was small (median 14 years versus 15 years). Table 2 shows similar characteristics among children with UC or IC. The only significant differences in this group were that overweight or obese children with UC or IC were more likely to have Medicaid insurance or to use methotrexate. There was also a nonsignificant increase in prednisone and infliximab use among obese or overweight children with UC/IC.
|n||Median (IQR) or %||n||Median (IQR) or %|
|Age (years)||822||15 (13-17)||205||14 (12-16)||<0.01|
|Gender (% female)||366||44.5||89||43.4||0.78|
|Disease duration (years)||822||2.9 (1.4-4.9)||205||2.7 (1.3-4.8)||0.31|
|Perianal disease (% yes)||103||12.5||32||15.6||0.24|
|Prior surgeryc (% yes)||87||10.6||30||14.6||0.10|
|Prior tube feeds (% yes)||21||2.6||5||2.4||0.93|
|Prednisone (% yes)||92||11.2||25||12.2||0.69|
|Infliximab (% yes)||216||26.3||60||29.3||0.39|
|Methotrexate (% yes)||49||6.0||9||4.4||0.38|
|Physician Global Assessment|
|n||Median (IQR) or %||n||Median (IQR) or %|
|Age (years)||399||15 (11–16)||172||14 (11–16)||0.34|
|Gender (% female)||211||52.9||100||58.1||0.25|
|Disease duration (years)||399||2.6 (1.1–4.8)||172||2.2 (1.0–4.4)||0.16|
|Perianal disease (% yes)||9||2.3||3||1.7||0.70|
|Prior surgeryc (% yes)||18||4.5||6||3.5||0.58|
|Prior tube feeds (% yes)||1||0.25||2||1.2||0.17|
|Prednisone (% yes)||63||15.8||35||20.4||0.19|
|Infliximab (% yes)||42||10.5||26||15.1||0.12|
|Methotrexate (% yes)||5||1.3||8||4.7||0.01|
|6MP/Azathioprine (% yes)||119||70.2||118||68.6||0.71|
|Physician Global Assessment|
Overall, the prevalence of overweight or obesity among children with CD was 20.0%. This rate was higher (30.1%) among children with UC or IC. In the overall IBD population, the prevalence was 23.6%. Table 3 shows a further breakdown of BMI-percentiles in children with CD or UC/IC. Children with UC/IC had greater rates of overweight, obese, and severely obese than patients with CD. The rate of overweight and obesity in children with UC/IC more closely mirrored the reported rate in the general population. Patients with CD had relatively greater percentages of underweight children when compared to patients with UC/IC (Table 3).
|BMI- percentile||Children with CD||Children with UC or IC||Total IBD, %|
Additional analyses were performed, limiting the population to only those children who were enrolled in the collaborative within 90 days of their initial IBD diagnosis (n = 426, 277 with CD, 149 with UC/IC). The prevalence of overweight and obesity in this group was essentially unchanged from the entire study population: 20.9% among patients with newly diagnosed CD and 34.9% among patients newly diagnosed with UC/IC. We then investigated the population of patients who reported Hispanic ethnicity, as this is a risk factor for overweight and obesity in the general population. The prevalence of overweight and obesity for the Hispanic population with IBD was 35.2% as compared to 23.1% among the non-Hispanic IBD population (P = 0.02). By disease subtype, the prevalence of overweight and obesity was 30.6% for CD and 40.0% for UC/IC in the Hispanic population. We finally performed a subanalysis further investigating any corticosteroid use. We defined any corticosteroid use as use at either the enrollment or most recent visit, in order to account for prior corticosteroid use. Among patients with CD, there was no difference in the rate of overweight and obesity (20.5% for those with any use of corticosteroids at prior or current visit, and 19.7% for nonusers, P = 0.8). A significant difference was found among patients with UC, with a rate of overweight and obesity of 35.0% for those with any use of corticosteroids at prior or current visit, as compared to 27.1% for nonusers (P = 0.05).
The independent effects via multivariate analysis of demographic and disease characteristics on overweight and obese status in children with IBD, presented overall and stratified by CD or UC/IC, are shown in Table 4. On adjusted analyses for patients with IBD and among the CD population, African-American race and having Medicaid insurance, rather than commercial insurance, were significantly associated with overweight and obese status. Among UC patients, the association between African-American race and Medicaid insurance and overweight/obese status did not reach statistical significance. Among patients with CD, prior surgery was significantly associated with overweight and obesity (adjusted odds ratio [OR] 1.73, 95% CI 1.07–2.82). In patients with CD, thiopurine use was inversely associated with overweight and obese status (adjusted OR 0.68, 95% CI 0.48–0.98). No other clinical disease characteristics were associated with overweight and obesity in children with IBD. Analyses were repeated with BMI-percentile as a continuous variable and the independent effects of predictors were found to be similar (data not shown).
|ORa||95% CI||ORa||95% CI||ORa||95% CI|
|At least 1||1.31||0.85-2.02||1.73||1.07-2.82||1.25||0.41-3.82|
|Disease duration (years)b||0.99||0.94-1.04||1.00||0.94-1.08||0.97||0.89-1.05|
Childhood obesity has become an epidemic in the U.S., with an estimated 31.7% meeting the definition of overweight or obese.3 The results of this study indicate that a substantial proportion of children with IBD, particularly UC or IC, are also either overweight or obese. This is important, as obesity may be associated with increased complications of disease and also with long-term cardiovascular and metabolic complications. In the adult IBD population, obesity has been associated with shorter time to development of perianal complications, more active disease, and more frequent hospitalizations.8 Furthermore, obesity-related comorbidities may indirectly affect IBD-related morbidity and mortality, as well as increase the potential for polypharmacy and medication interactions. The pathophysiology of obesity supports the association with increased severity of disease. Obesity can be considered a chronic low-grade state of inflammation. In obesity, adipose tissue can undergo a transformation and become infiltrated by macrophages.14 In addition, many proinflammatory markers linked to obesity and adipose tissue (including leptin, adiponectin, resistin, and ghrelin) have also been linked to IBD.15, 16 These markers may become upregulated, contributing to disease activity.
The results of this study are consistent with the results of a previously published study of newly diagnosed (untreated) CD and UC from two separate North American cohorts initiated in 2000. Kugathasan et al10 found that most children with CD or UC had a BMI percentile in the normative range. However, 10% of children with CD and 20%–30% of children with UC were overweight or at risk for overweight (with new consensus definition, this would represent overweight or obese). In the present study of treated IBD, we found even greater rates of overweight and obesity. Similar to Kugathasan et al, we also found higher rates of overweight and obesity among children with UC/IC as compared to CD, although CD patients still had a 20% prevalence of overweight or obesity.
Similar to adult IBD populations,8 the results of this study also indicate that pediatric patients with CD who are either overweight or obese have had higher rates of IBD-related surgery. In UC/IC, this trend did not reach statistical significance. These pediatric data, in combination with prior adult data, suggest that obesity in IBD may be an independent predictor of a more complicated disease course.
The early literature on pediatric IBD found associations between weight and growth retardation and juvenile onset of IBD, especially CD.9 Malnutrition is even a component of the most commonly used disease severity indices in CD, the Crohn's Disease Activity Index (CDAI) and the Pediatric Crohn's Disease Activity Index (PCDAI). Since the earliest descriptions of IBD, a greater number of medications have become available for treatment and both CD and UC may be recognized earlier in the course of the disease. For these reasons, malnourishment may no longer be a common manifestation of treated pediatric IBD. Rather, children with IBD may now be following the course of the rest of the population, with a greater percentage overweight or obese than ever before.
The factors we found to be associated with overweight and obesity, including non-Caucasian race and Medicaid insurance status (a proxy for lower socioeconomic status), have also been shown to be associated with overweight and obesity in the general pediatric population.3 We also found thiopurine use to be inversely associated with overweight and obesity in patients with CD. We speculate that current thiopurine use may be a marker for prior disease severity associated with malabsorption. Environmental factors such as excess energy consumption and decreased physical activity can exacerbate the tendency towards obesity in all children,4 regardless of chronic disease status. Appropriate lifestyle interventions for obesity, including dietary modifications and increased physical activity, are important for all overweight or obese children, including those with IBD.
Surprisingly, we found few associations between current medication use and overweight and obese status. Current prednisone use was not associated with overweight and obese status in CD, although a nonsignificant trend was observed in UC. Perhaps this reflects the fact that prednisone use was reserved for the treatment of more severe disease, the population of patients which might have had the lowest BMI prior to corticosteroid initiation. Alternatively, it may only be prior use of corticosteroids that is associated with overweight and obese status, as the weight gain occurs over time. We did account for prior corticosteroid use in subanalyses (corticosteroid use at the time of enrollment or subsequent visit). We were unable to account for all prior corticosteroid use, as we only had information on current use at the time of visit. This may have contributed to the lack of association in patients with CD. We did find a significant increase in the prevalence of overweight and obesity in patients with UC/IC on prior or current corticosteroids. Of note, we also found a small and nonsignificant association between current infliximab use and overweight and obese status, an observation often noted in clinical practice.
There are several strengths to this multicenter study. We were able to study a large number of children with IBD, allowing for more precise estimates of BMI percentiles. The centers included in the ImproveCareNow collaborative represent a mixture of private, not-for-profit, and academic centers of various sizes and from all regions of the U.S., increasing the generalizability of these results. The database also contained extensive data on clinical disease characteristics, including duration of disease, phenotype, assessment of severity, and prescribed medications. Therefore, we were able to control for many potential confounders of the relationship between IBD and overweight and obese status.
There are several limitations to this study. The cross-sectional design of this analysis precludes definitive causal inferences regarding associations between BMI and specific disease characteristics or medication utilization. In addition, confirmation of clinical variables in the database, other than anthropometrics, was beyond the scope of this study. However, we did ask sites to confirm outlying height and weight measurements and found these to be remarkably accurate, with very few errors (<3%). Also, the proportion of overweight and obesity in any given population will vary according to where the continuous variable for BMI is dichotomized. We did perform additional analyses using BMI-percentile as a continuous variable and found similar results. A priori, we chose to use standard definitions of overweight and obesity consistent with the CDC BMI-for-age growth charts. Use of other standards might result in other proportions, but would be unlikely to significantly change the independent effects of demographic and disease characteristics seen in our model.
In summary, overweight and obesity are common in pediatric IBD. Little is still known about how childhood obesity will affect the adult outcomes of patients with IBD. The results of this study have important implications for the care of children with IBD. It is important for providers to recognize that CD and UC/IC can exist in overweight and obese patients, and that the traditional description of malnourishment in pediatric IBD may no longer represent the majority of cases. Because gastroenterologists have unique expertise in nutrition and improved access to dieticians and other multidisciplinary resources, screening, counseling, and treatment for overweight and obesity should be the standard of care for the patient with IBD. Lifestyle modifications, including dietary modification and physical activity, are important for all overweight and obese children, including those with IBD. Further studies on the relationship between obesity and inflammation in the pediatric population are warranted.
- 112000 CDC Growth Charts for the United States: methods and development. Vital Health Stat 11 2002: 1–190., , , et al.
- 13Short pediatric Crohn's disease activity index for quality improvement and observational research. Inflamm Bowel Dis. 2010 [Epub ahead of print]., , , et al.
Actively Enrolling Sites in the ImproveCareNow Pediatric IBD Collaborative
Nationwide Children's Hospital, Columbus, OH Inova Pediatric Digestive Disease Center, Fairfax, VA Nemours Children's Clinic University of North Carolina at Chapel Hill, Chapel Hill, NC The Barbara Bush Children's Hospital, Portland, ME Loyola University, Chicago, IL University of Oklahoma, Oklahoma City, OK University of Vermont, Burlington, VT Emory University, Atlanta, GA Children's Medical Center of Dallas, Dallas, TX Pediatric Gastroenterology & Nutrition Associates, Las Vegas, NV Massachusetts General Hospital, Boston, MA Oakland Children's Hospital, Oakland, CA