- About this Journal
- Abstracting and Indexing
- Aims and Scope
- Article Processing Charges
- Articles in Press
- Author Guidelines
- Bibliographic Information
- Citations to this Journal
- Contact Information
- Editorial Board
- Editorial Workflow
- Free eTOC Alerts
- Publication Ethics
- Reviewers Acknowledgment
- Submit a Manuscript
- Subscription Information
- Table of Contents
Journal of Environmental and Public Health
Volume 2012 (2012), Article ID 635097, 6 pages
History of Cesarean Section Associated with Childhood Onset of T1DM in Newfoundland and Labrador, Canada
1Newfoundland and Labrador Centre for Health Information, St. John's, NL, Canada A1B 2C7
2Janeway Pediatric Research Unit, 4th Floor Janeway Hostel, Memorial University of Newfoundland, 300 Prince Philip Drive, St. John's, NL, Canada A1B 3V6
3Janeway Children's Health and Rehabilitation Centre, 300 Prince Philip Drive, St. John's, NL, Canada A1B 3V6
Received 27 February 2012; Accepted 20 April 2012
Academic Editor: V. Mohan
Copyright © 2012 J. Phillips et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Objectives. Newfoundland and Labrador (NL) has one of the highest incidences of Type 1 diabetes mellitus (T1DM) worldwide. Rates of T1DM are increasing and the search for environmental factors that may be contributing to this increase is continuing. Methods. This was a population-based case control design involving the linkage of data from a diabetes database with live birth registration data. 266 children aged 0####^~^~^~^~^~^####x2013;15 years with T1DM were compared to age- and gender-matched controls. Chi-square analysis and multivariate conditional logistic regression were carried out to assess maternal and infant factors (including maternal age, marital status, education, T1DM, hypertension, birth order, delivery method, gestational age, size-for-gestational-age, and birth weight). Results. Cases of T1DM were more likely to be large-for-gestational-age () and delivered by C-section () as compared to controls. C-section delivery was associated with increased risk of T1DM (HR 1.41, ) when birth weight and gestational age were included in the model, but not when size-for-gestational-age was included (HR 1.3, ). Conclusions. Birth by C-section was found to be a risk factor for the development of T1DM in a region with high rates of T1DM and birth by C-section. These findings may have an impact on health practice, health care planning, and future research.
Type 1 diabetes mellitus (T1DM) is one of the most common chronic diseases in childhood and results from autoimmune destruction of pancreatic ####^~^~^~^~^~^####x3b2;-cells, leading to insulin deficiency. T1DM is thought to originate through a combination of genetic and unknown environmental factors, of which environmental factors remain poorly defined. Newfoundland and Labrador (NL), Canada, is recognized as having one of the highest rates of T1DM worldwide . A study on hospitalizations of children in NL reported an increase in diabetes-related hospitalizations among children aged 0####^~^~^~^~^~^####x2013;19 years . T1DM is a significant disease in NL with its associated acute and chronic complications as well as the economic costs to both families and the health care system. Identification of potential perinatal environmental risk factors is examined in this study to try and elucidate potential reasons of why the disease is so common in this region of North America.
This study was a case control design involving the linkage of data extracted from the Newfoundland and Labrador Diabetes Database (NLDD) with the Live Birth System (LBS). The NLDD is maintained by the Janeway Pediatric Research Unit at the Janeway Child Health Care Centre (JCHCC) in St. John####^~^~^~^~^~^####x2019;s, NL. The JCHCC is the only tertiary care pediatric hospital in the province. The NLDD includes data for the majority of cases of T1DM diagnosed in NL from 1987 to present. Children are included in the database as part of a prospective provincial study on the epidemiology of T1DM in NL. They have a confirmed diagnosis of T1DM according to Canadian Diabetes Association (CDA) criteria . The LBS is maintained by the Newfoundland and Labrador Centre for Health Information (NLCHI). Data for this system are acquired from Live Birth Notification forms that are completed in all provincial health care facilities. The forms are provided to NLCHI by the Vital Statistics Division, Service NL, and contain clinical and demographic data for all births (resident and nonresident) in the province. The system currently contains data on all births from 1992 to 2011.
Patient records were individually linked across datasets. Cases included children born in NL from 1992 onwards which have been diagnosed with T1DM before 15 years of age. Children with type 2 diabetes, maturity-onset diabetes of youth, transient hyperglycemia, and diabetes caused by chemotherapy or cystic fibrosis are excluded from the NLDD and thus were not included in the study. Children born prior to 1992 were not included in the study because there are no electronic birth notification data available before this date.
A unique identifier, such as the provincial health insurance plan number, was not available for all children in the NLDD. As a result case subjects were linked to the LBS using child####^~^~^~^~^~^####x2019;s date of birth and mother####^~^~^~^~^~^####x2019;s maiden name. Where available, child####^~^~^~^~^~^####x2019;s name was used to verify the linkage. Of the 301 cases in the NLDD, 23 were excluded because they were born out of province. Of the remaining 278, 6 were excluded as duplicate records. Linkage was possible for all but six children resulting in a total of 266 cases included in the study. Three control subjects () were selected for each case matched on year of birth, sex, and health authority of mother####^~^~^~^~^~^####x2019;s residence at time of delivery. Power analysis was performed to determine whether this sample size would be sufficient to detect statistical significant associations between T1DM and the risk factors of interest. The power analysis was conducted considering an overall rate of birth by C-section in NL as 30.9####^~^~^~^~^~^####x25; , in order to achieve a power of 80####^~^~^~^~^~^####x25; with a desired odds ratio of 1.5. Using the method described by Kelsey et al.  the power analysis confirmed that a sample size of 266 cases and 798 controls is sufficient to detect statistically significant relationships between T1DM and delivery by C-section.
Cases and controls were grouped into two gestational age categories: preterm and term/postterm. Birth weight in grams was used to classify cases and controls as high birth weight (####^~^~^~^~^~^####x3e;4,000 grams) or not (####^~^~^~^~^~^####x2264;4,000 grams). Cases and controls were also classified as small/appropriate-for-gestational-age or large-for-gestational-age using the method described by Kramer et al. . Method of delivery was categorized as vaginal or C-section. Cases and controls were grouped according to parity or birth order as either 1 and 2 or more. Mother####^~^~^~^~^~^####x2019;s age in years was classified as ####^~^~^~^~^~^####x2264;34 years or ####^~^~^~^~^~^####x3e;34 years. Mothers were also classified by their T1DM status and hypertension status. Mother####^~^~^~^~^~^####x2019;s marital status was categorized as married, single, separated, widowed, or divorced. Mother####^~^~^~^~^~^####x2019;s education level was classified into three categories: not graduated high school, graduated high school, and education beyond high school.
Descriptive statistics were generated to describe the distribution of cases and controls. Demographic and clinical factors of mothers, including age, marital status, education, place of residence, parity (number of live born children delivered), and complications of pregnancy, were included. Cases and controls were analyzed by sex, place of residence, age of onset, length of gestation, type of delivery, birth weight, size for gestational age, and birth order.
Chi-square tests were used to predict diabetes status on the basis of the independent variables. Conditional multiple logistic regression was used to assess the relationship between T1DM risk and the variables of interest. Two conditional logistic regression models were employed. The first model contained birth weight, gestational age, parity, delivery method, mother####^~^~^~^~^~^####x2019;s marital status, mother####^~^~^~^~^~^####x2019;s education level, mother####^~^~^~^~^~^####x2019;s age, maternal hypertension, and mother####^~^~^~^~^~^####x2019;s T1DM status. The second model incorporated all variables in the first model with the exception of birth weight and gestational age which were replaced with size-for-gestational-age. Birth weight and gestational age were not included in the same model as size-for-gestational-age as they are components of this variable.
The Statistical Package for the Social Sciences (SPSS) 17.0 was used to generate descriptive statistics and chi-squares. SAS 9.2 was used to conduct the conditional multivariate logistic regressions.
This study received approvals from the Human Investigation Committee of Memorial University, from each of the hospital boards and the Secondary Uses Committee of the Newfoundland and Labrador Centre for Health Information (NLCHI) prior to commencement.
Table 1 presents the descriptive characteristics of the cases of T1DM. The percentages of male and female cases were similar (50.8 and 49.2, resp.). Table 1 also demonstrates the age distribution of cases as well as their age of diagnosis. There were more males than females diagnosed in the 0####^~^~^~^~^~^####x2013;4 age group; however, this finding was not statistically significant.
Table 2 presents maternal and perinatal characteristics of the study population. A higher percentage of cases than controls were born pre-term (9.8####^~^~^~^~^~^####x25; versus 6.8####^~^~^~^~^~^####x25;, resp.). While there was no significant difference observed between birth weight of the cases and controls, there was a significant difference observed for size-for-gestational-age with a higher percentage of cases than controls born large-for-gestational-age (18.2####^~^~^~^~^~^####x25; versus 12.8####^~^~^~^~^~^####x25;, resp., ). It was more common for cases to be delivered by C-section than controls (30.8####^~^~^~^~^~^####x25; versus 22.1####^~^~^~^~^~^####x25;, ). T1DM was more common among first or second born cases compared to those born third or higher (.
Table 3 presents the results of the conditional logistic regression models. In the model which included birth weight and gestational age, delivery by C-section was associated with increased risk of T1DM. Children delivered by C-section were 1.41 times as likely to develop T1DM (Hazard ratio (HR) 1.41, ). In the second model, which included size-for-gestational-age, C-section delivery was not associated with increased risk of T1DM (HR 1.3, ). Both parity and size-for-gestational-age were found to be significant risk factors for T1DM from chi-square analysis (Table 2); these factors did not remain statistically significant in the conditional logistic regression models.
Findings of this study indicate that C-section delivery was a significant risk factor for T1DM in children aged 0####^~^~^~^~^~^####x2013;15 years. This finding is in line with a recent meta-analysis of 20 studies which found that the combined effect of C-section delivery was 1.23 (95####^~^~^~^~^~^####x25; CI 1.15####^~^~^~^~^~^####x2013;1.32) . Theories of why this may be associated with the development of T1DM in offspring includes the involvement of the role of gut bacteria in the development of the immune system . Studies have shown a difference between the compositions of gut microbiota in vaginally delivered children and those delivered by C-section. Children delivered by C-section may be primarily exposed to bacteria in the hospital and not maternal bacteria, hence the increased risk of T1DM may be linked to a different composition of gut flora . Another possible explanation is related to the hygiene hypothesis which proposes that the risk of diabetes may be increased when children are not exposed to infections in early life . Children delivered by C-section have decreased exposures to infections compared to children born vaginally and, in turn, have increased risk for diabetes . Another theory suggests that the observed increased risk of diabetes after C-section may be related to perinatal stress . NL has a high rate of birth by C-section as compared to other regions in Canada. The provincial rate of births by C-section was 30.9####^~^~^~^~^~^####x25; in 2005-2006 versus the Canadian rate of 26.3####^~^~^~^~^~^####x25; . The rates of C-section have increased in NL to 33####^~^~^~^~^~^####x25; in 2010 .
In the present study, maternal age at time of birth was not found to be significantly associated with risk of T1DM in offspring; other studies have found significant relationships between mother####^~^~^~^~^~^####x2019;s age and T1DM risk. A recent meta-analysis of 37 studies found that the odds of T1DM increased by 10####^~^~^~^~^~^####x25; for children whose mothers were over 35 years of age at time of birth (OR = 1.10 95####^~^~^~^~^~^####x25; CI 1.01, 1.20; ) . Conversely, a matched case-control study of 196 cases in the United Kingdom  found that mothers of control children were older than mothers of cases (OR = 0.900 95####^~^~^~^~^~^####x25; CI 0.854, 0.948; ). For other maternal factors, such as education level and marital status, there were no associations found which is consistent with other similar studies [14, 15]. The present study also did not find any associations between maternal hypertension and risk of T1DM in offspring. Other studies have found an increased risk of T1DM in offspring with maternal history of T1DM [13, 16, 17]; however, these studies also included information on paternal history of T1DM. A 2009 study by Algert and colleagues  did not find an association between maternal T1DM and risk of T1DM in children. Similar to the present study, the study by Algert et al. did not contain information on paternal T1DM.
There was no significant relationship between parity and T1DM risk found in the current study. This is different than a Western Australia population based cohort study of 835 cases of T1DM diagnosed by the age of 15 that found a significant decrease in T1DM with increasing birth order .
Birth weight and gestational age were not found to be associated with risk of T1DM in the present study; however, chi-squared analysis revealed a significant difference between T1DM and size-for-gestational-age with a higher percentage of cases than controls born large-for-gestational-age, but this was no longer significant in the conditional logistic regression models. Our findings do not support the findings of a meta-analysis of 11 studies examining birth weight which found that a birth weight greater than 4,000 grams was associated with an increased odds of T1DM (OR = 1.17 95####^~^~^~^~^~^####x25; CI 1.09, 1.26; ) . Findings related to the association between gestational age and T1DM appear to be mixed. A case-control study conducted in Austria found that babies born at 34####^~^~^~^~^~^####x2013;39 weeks had a significantly higher risk for T1DM compared to those born before 33 or after 40 weeks . However, a study by Cardwell et al.  found that children born after 40 weeks gestation had a significantly lower risk of T1DM than children born prior to 40 weeks. While size-for-gestational-age has not been extensively studied, some studies have found significant associations. A cohort study of 272 children in New South Wales, Australia, with T1DM found that children who were small-for-gestational-age had a significantly decreased risk of T1DM compared to children born appropriate-for-gestational age .
The findings of this study should be considered in the context of its strengths and weaknesses. An important strength is that the use of a record linkage case-control study design eliminates recall bias that is apparent in cross-sectional study designs. Secondly, data contained in the LBS were collected at time of birth by healthcare professionals, and the NLDD data were collected from physician charts at time of T1DM diagnosis which contributes to the reliability of the data. A limitation of this study is that there was very little information available pertaining to fathers as the majority of the information collected at the time of birth for the LBS is related to the mother and child. Thus, paternal factors and family history could not be considered for analysis.
This study identified C-section as a significant risk factor for the development of T1DM among children aged 0####^~^~^~^~^~^####x2013;15 years in NL, a region with very high rates of T1DM. Findings may have an impact on health practice, health care planning and future research related to T1DM among children. Further research should be undertaken to understand the nature of this association.
L. A. Newhook is the senior investigator and was responsible for the intellectual conception and design of the study, funding application, paper preparation and is the guarantor of the research. J. Phillips was responsible for overall coordination of the study and contributed intellectually to the methods, literature review, database development, analysis, logistics, paper preparation, and approvals. N. Gill contributed intellectually to the methods, database development, analysis, logistics, and approvals. S. Penney was the research nurse who was responsible for study approvals, as well as gathering, confirming, and entering of data and maintaining the NLDD. K. Sikdar was responsible for overseeing the statistical analysis. All authors contributed to and approved the final paper submission.
This study was funded by the AR Cox Research Award, Memorial University. Thanks are due to the diabetes nurses across the province of NL for their efforts and support of diabetes research. Authors wish to acknowledge the efforts of Tracy Parsons who performed the data linkage for this project. There are no conflict of interests to disclose.
- L. A. Newhook, M. Grant, A. Sloka et al., “Very high and increasing incidence of type 1 diabetes mellitus in Newfoundland and Labrador, Canada,” Pediatric Diabetes, vol. 9, part 2, no. 3, pp. 62–68, 2008.
- R. Alaghehbandan, K. D. Collins, L. A. Newhook, and D. MacDonald, “Childhood type 1 diabetes mellitus in Newfoundland and Labrador, Canada,” Diabetes Research and Clinical Practice, vol. 74, no. 1, pp. 82–89, 2006.
- Canadian Diabetes Association, Canadian Diabetes Association 2008 Clinical Practice Guidelines, Canadian Diabetes Association, 2008.
- Canadian Institute for Health Information, Giving Birth in Canada: Regional Trends from 2001-2002 to 2005-2006, Canadian Institute for Health Information, 2007.
- J. L. Kelsey, A. S. Whittemore, A. S. Evans, and W. D. Thomson, Methods in Observational Epidemiology, Oxford University Press, Oxford, UK, 2nd edition, 1996.
- M. S. Kramer, R. W. Platt, S. W. Wen et al., “A new and improved population-based Canadian reference for birth weight for gestational age,” Pediatrics, vol. 108, no. 2, article E35, 2001.
- C. R. Cardwell, L. C. Stene, G. Joner et al., “Caesarean section is associated with an increased risk of childhood-onset type 1 diabetes mellitus: a meta-analysis of observational studies,” Diabetologia, vol. 51, no. 5, pp. 726–735, 2008.
- J. Penders, C. Thijs, C. Vink et al., “Factors influencing the composition of the intestinal microbiota in early infancy,” Pediatrics, vol. 118, no. 2, pp. 511–521, 2006.
- E. A. Gale, “A missing link in the hygiene hypothesis?” Diabetologia, vol. 45, no. 4, pp. 588–594, 2002.
- G. Dahlquist and B. Kallen, “Maternal-child blood group incompatibility and other perinatal events increase the risk for early-onset type 1 (insulin-dependent) diabetes mellitus,” Diabetologia, vol. 35, no. 7, pp. 671–675, 1992.
- Research and Evaluation Department: Newfoundland Centre for Health Information, “Live Birth Trends 2006–2010,” 2011.
- C. R. Cardwell, L. C. Stene, G. Joner et al., “Maternal age at birth and childhood type 1 diabetes: a pooled analysis of 30 observational studies,” Diabetes, vol. 59, no. 2, pp. 486–494, 2010.
- A. L. Marshall, A. Chetwynd, J. A. Morris et al., “Type 1 diabetes mellitus in childhood: a matched case control study in Lancashire and Cumbria, UK,” Diabetic Medicine, vol. 21, no. 9, pp. 1035–1040, 2004.
- S. Sipetic, H. Vlajinac, N. Kocev, and S. Saji, “The Belgrade childhood diabetes study: prenatal and social associations for type 1 diabetes,” Paediatric and Perinatal Epidemiology, vol. 18, no. 1, pp. 33–39, 2004.
- S. B. Sipetic, H. D. Vlajinac, N. I. Kocev, J. M. Marinkovic, S. Z. Radmanovic, and M. D. Bjekic, “The Belgrade childhood diabetes study: a multivariate analysis of risk determinants for diabetes,” European Journal of Public Health, vol. 15, no. 2, pp. 117–122, 2005.
- J. Svensson, B. Carstensen, H. B. Mortensen, and K. Borch-Johnsen, “Early childhood risk factors associated with type 1 diabetes—is gender important?” European Journal of Epidemiology, vol. 20, no. 5, pp. 429–434, 2005.
- A. Haynes, C. Bower, M. K. Bulsara, J. Finn, T. W. Jones, and E. A. Davis, “Perinatal risk factors for childhood type 1 diabetes in Western Australia—a population-based study (1980–2002),” Diabetic Medicine, vol. 24, no. 5, pp. 564–570, 2007.
- C. S. Algert, A. McElduff, J. M. Morris, and C. L. Roberts, “Perinatal risk factors for early onset of type 1 diabetes in a 2000–2005 birth cohort,” Diabetic Medicine, vol. 26, no. 12, pp. 1193–1197, 2009.
- T. Harder, K. Roepke, N. Diller, Y. Stechling, J. W. Dudenhausen, and A. Plagemann, “Birth weight, early weight gain, and subsequent risk of type 1 diabetes: systematic review and meta-analysis,” American Journal of Epidemiology, vol. 169, no. 12, pp. 1428–1436, 2009.
- T. Waldhoer, B. Rami, E. Schober et al., “Perinatal risk factors for early childhood onset type 1 diabetes in Austria—a population-based study (1989–2005),” Pediatric Diabetes, vol. 9, part 1, no. 3, pp. 178–181, 2008.
- C. R. Cardwell, D. J. Carson, and C. C. Patterson, “Parental age at delivery, birth order, birth weight and gestational age are associated with the risk of childhood type 1 diabetes: a UK regional retrospective cohort study,” Diabetic Medicine, vol. 22, no. 2, pp. 200–206, 2005.