Abstract
Purpose
We tested the hypothesis that cesarean section might increase the risk for allergic diseases compared to vaginal delivery, by depriving the newborn of exposure to maternal microflora.
Methods
We evaluated the prevalence of allergic diseases, allergic inflammation, and allergic sensitization according to mode of delivery for 279 Korean children aged ≤16 years. Data were extracted from medical records and a questionnaire filled out by parents. Logistic regression was used to determine the association between cesarean section and the outcomes of interest.
Results
Of the 279 children, 179 (62.6%) were delivered vaginally and 100 (37.4%) by cesarean section. There were no differences in the prevalence of allergic diseases, allergic inflammation, or allergic sensitization according to mode of delivery. Children born by cesarean section had no higher risk of allergic disease than those delivered vaginally, regardless of a parental history for allergic disease. Adjusted odds ratios (95% confidence intervals) for cesarean section compared to vaginal delivery were not statistically significant for any outcome considered: asthma, 0.76 (0.37-1.57), allergic rhinitis, 1.14 (0.61-2.10), atopic dermatitis, 1.01 (0.59-1.71).
The prevalence of allergic diseases is increasing due to rapid industrialization, changes in lifestyle, air pollution, and the occurrence of new allergens. The 2002-2003 phase 3 study performed by the International Study of Asthma and Allergies in Childhood (ISAAC) reported that the prevalence of bronchial asthma, allergic rhinitis, and atopic dermatitis tended to increase in most institutions compared to data from 5 years earlier (provided in a report by the ISAAC phase 1 study).1 The relationship between the prevalence of allergic diseases and mode of delivery in childbirth has been actively investigated as the proportion of cesarean sections has increased.2 In the United States, the frequency of cesarean sections increased from 23.0% in 1990 to 28.0% in 2003 and to 31.1% in 2006.3,4 According to the Korean Health Insurance Review and Assessment Service, the rate of cesarean sections continuously increased from 13.3% in 1990 to 40.5% in 2001, but decreased to 36.0% in 2006, although this rate was considerably higher than that proposed by the World Health Organization (WHO, 5-15%). Cesarean section babies have a different gut flora, which has been suggested to prolong immunological immaturity and thereby increase the risk for the development of allergic disease.5-7 The hygiene hypothesis states that decreased exposure to microorganisms early in life leads to insufficient stimulation of Th1 lymphocytes and, therefore, a predominance of the Th2 allergic response.8 However, the association between mode of delivery and the prevalence of allergic diseases has not been completely elucidated. Some investigators have reported increased risk for developing asthma among children born by cesarean section compared to those born by vaginal delivery,9-12 whereas others have found no such relationship.13-15 Although the relationship between mode of delivery and the prevalence of allergic diseases has been investigated continuously in many countries, there has been no report on this relationship in Korea. Therefore, we investigated the effects of mode of delivery on the prevalence of allergic diseases in Korean children.
A total of 279 children aged ≤16 years who visited Severance Children's Hospital, Yonsei University College of Medicine between January and December 2008.
The following data were identified through a questionnaire: gender, age, mode of delivery, gestational age, birth weight, history of admission to a neonatal intensive care unit (NICU), duration of breast feeding, maternal age at delivery, exposure to household pets or smoking, and physician-diagnosed allergic diseases in the children and their parents. Data on the diagnosis of allergic diseases, allergic inflammation, and allergic sensitization were collected from medical records and analyzed retrospectively. We evaluated the relationship between mode of delivery and prevalence of three common childhood allergic diseases: asthma, allergic rhinitis, and atopic dermatitis.
Bronchial asthma was defined as recurrent wheezing or coughing episodes in the absence of the common cold in the preceding 12 months. In addition, a physician's diagnosis of bronchial hyperresponsiveness upon methacholine challenge (PC20 ≤16 mg/mL) and at least a 12% reversibility of forced expiratory volume in 1 second (FEV1) after inhaling a β2 agonist, as per the American Thoracic Society (ATS) criteria,16 were required. A diagnosis of allergic rhinitis was made according to the WHO guidelines "Allergic Rhinitis and its Impact on Asthma,"17 and a diagnosis of atopic dermatitis was made based on the diagnostic criteria proposed by Hanifin and Rajka (1980).18
Serum-specific IgE against Dermatophagoides farinae (Df ) and Dermatophagoides pteronyssinus (Dp) and serum total IgE were measured using the CAP radioallergosorbent technique (UniCAP; Phadia, Uppsala, Sweden). The NE-8000 system (Sysmex, Kobe, Japan) was used to automatically count eosinophils in peripheral blood. Allergic sensitization was identified in 177 (63.4%) of the 279 subjects.
Skin-prick tests, using 65 inhalant and food allergens, were performed on 41 subjects who had not taken antihistamines before the test. Normal saline was used as a negative control, and a 0.1% histamine solution was used as a positive control. Test results were considered positive if the following criteria were met: (1) there was no erythema or wheal in response to the negative control and (2) the allergen/histamine wheal size ratio was ≥1 or (3) the wheal measured ≥3 mm. Atopy was defined as a positive reaction to one or more allergens, a specific IgE level of ≥0.35 kU/L, or a serum total IgE level of ≥100 kU/L.
The clinical characteristics between the cesarean and vaginal delivery groups were compared using the Student's t-test, the chi-square test, and the Fisher's exact test. The effects of confounding variables were removed by logistic regression analysis. Statistical analyses were performed using SPSS version 13.0 (SPSS Inc, Chicago, IL, USA). A P value <0.05 was considered statistically significant.
Of the 279 subjects, 179 (62.6%) were born by vaginal delivery, and 100 (37.4%) were born by cesarean section. The mean (±SD) age of the subjects was 4.6 (±3.8) years. Atopy was assessed in 197 subjects (70.6%). There were no significant differences between the two groups for gender, gestational age, birth weight, season of birth, maternal age at birth, the number of family members, birth order, duration of breast feeding, admission to NICU, exposure to household pets or smoking, or a parental history of allergic diseases. Furthermore, there were no significant differences in blood eosinophil counts or serum total IgE levels between the two groups (Table 1).
The prevalence of bronchial asthma, allergic rhinitis, and atopic dermatitis did not differ significantly between the two groups, nor did sensitization to Dp or Df (Table 2). There were also no significant differences in the odds ratios for the prevalence of allergic diseases, sensitization to Dp or Df, or after adjusting for confounding variables including age, gender, gestational age, birth weight, duration of breast feeding, and a parental history of allergic diseases (Table 3).
The subjects were divided into three subgroups: those with both parents, one parent, and no parent with a history of allergic disease. The prevalence of allergic diseases according to mode of delivery was not significantly different among the three subgroups. In addition, there were no significant differences among the odds ratios of each group after adjusting for confounding variables including age, gender, gestational age, birth weight, and maternal age at birth (Table 4).
Mode of delivery in childbirth has been implicated in the development of allergic disorders during childhood.19 According to the Nationwide Study of Asthma and Allergies in Korean Children, the prevalence of the three allergic diseases studied herein increased from 1995 to 2000 as follows: for asthma, from 7.7% to 9.1% in elementary school students, and from 2.7% to 5.3% in middle school students; for allergic rhinitis, from 15.5% to 20.4%, and from 7.7% to 13.6%, respectively; and for atopic dermatitis, from 16.6% to 24.9%, and from 7.3% to 12.8%, respectively.20 Because the rate of cesarean sections in Korea is relatively high compared to other countries,21 investigating the association between mode of delivery and the prevalence of allergic diseases is warranted. However, no study has considered this association in Korea. We found no significant differences between the cesarean section and vaginal delivery groups for the prevalence of allergic diseases, blood eosinophil counts, serum total IgE levels, or allergic sensitization to Dp and Df. The prevalence of allergic diseases according to mode of delivery was not significantly different between the three subgroups classified by a parental history of allergic diseases.
Although we analyzed confounding variables including age, gender, mode of delivery, gestational age, birth weight, admission to NICU, duration of breast feeding, maternal age at birth, exposure to household pets or smoking, physician-diagnosed allergic diseases, and a parental history of allergic diseases, we were unable to collect data on other variables, including parental educational level, residence, the time infants spent in a nursery, antibiotic administration at NICU admission, or peripartum complications.
This study has some limitations. It was a retrospective study with a small sample size, and it included subjects from a single institution and a wide range of age groups. Furthermore, it is possible that bias could have been introduced in the data that were collected through a questionnaire, and the insignificant differences in blood eosinophil counts, serum total IgE levels, and allergic sensitization to allergens may be explained by the fact that we did not perform these tests on all subjects.
Cesarean sections are associated with delayed intestinal colonization,6 which could deprive newborns of immunostimulatory impulses at a very critical period in life when the immune system and the gut barrier mature.7 Cesarean sections may also be associated with a lack of IL-10 or TGF-β production, which may redirect the constitutive Th2-phenotype of the newborn to normal.22,23 A recent meta-analysis reported that cesarean sections increase the subsequent risk of asthma in children by 20%,24 and lead to an increased risk for allergic rhinitis and atopy among children with a parental history of asthma due to allergies.25 Koplin et al.26 indicated that cesarean sections increase the risk for sensitization to food allergens. In contrast, some investigators have proposed that mode of delivery is not related to allergic diseases such as asthma in children.19,27 Therefore, although cesarean sections are considered a risk factor for allergic diseases, a definite association has not yet been determined. Moreover, such studies have shown different results according to the duration of follow-up, investigated variables, and the definition of allergic diseases.
In conclusion, this is the first study to investigate whether there is an association between mode of delivery in childbirth and the prevalence of allergic diseases in Korea, and we did not find a significant correlation. Further cohort studies with a larger sample size are needed to confirm our findings.
References
1. Asher MI, Montefort S, Björkstén B, Lai CK, Strachan DP, Weiland SK, Williams H. ISAAC Phase Three Study Group. Worldwide time trends in the prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and eczema in childhood: ISAAC Phases One and Three repeat multicountry cross-sectional surveys. Lancet. 2006. 368:733–743.
2. Bager P, Wohlfahrt J, Westergaard T. Caesarean delivery and risk of atopy and allergic disease: meta-analyses. Clin Exp Allergy. 2008. 38:634–642.
3. Menacker F. Trends in cesarean rates for first births and repeat cesarean rates for low-risk women: United States, 1990-2003. Natl Vital Stat Rep. 2005. 54:1–8.
4. Hamilton BE, Martin JA, Ventura SJ. Births: preliminary data for 2006. National vital statstics reports. 2007. Hyattsville (MD): National Center for Health Statistics.
5. Bennet R, Nord CE. Development of the faecal anaerobic microflora after caesarean section and treatment with antibiotics in newborn infants. Infection. 1987. 15:332–336.
6. Gronlund MM, Lehtonen OP, Eerola E, Kero P. Fecal microflora in healthy infants born by different methods of delivery: permanent changes in intestinal flora after cesarean delivery. J Pediatr Gastroenterol Nutr. 1999. 28:19–25.
7. Grönlund MM, Arvilommi H, Kero P, Lehtonen OP, Isolauri E. Importance of intestinal colonisation in the maturation of humoral immunity in early infancy: a prospective follow up study of healthy infants aged 0-6 months. Arch Dis Child Fetal Neonatal Ed. 2000. 83:F186–F192.
8. Strachan DP. Hay fever, hygiene, and household size. BMJ. 1989. 299:1259–1260.
9. Xu B, Pekkanen J, Jarvelin MR. Obstetric complications and asthma in childhood. J Asthma. 2000. 37:589–594.
10. Kero J, Gissler M, Grönlund MM, Kero P, Koskinen P, Hemminki E, Isolauri E. Mode of delivery and asthma - is there a connection? Pediatr Res. 2002. 52:6–11.
11. Renz-Polster H, David MR, Buist AS, Vollmer WM, O'Connor EA, Frazier EA, Wall MA. Caesarean section delivery and the risk of allergic disorders in childhood. Clin Exp Allergy. 2005. 35:1466–1472.
12. Bager P, Melbye M, Rostgaard K, Benn CS, Westergaard T. Mode of delivery and risk of allergic rhinitis and asthma. J Allergy Clin Immunol. 2003. 111:51–56.
13. Bernsen RM, de Jongste JC, Koes BW, Aardoom HA, van der Wouden JC. Perinatal characteristics and obstetric complications as risk factors for asthma, allergy and eczema at the age of 6 years. Clin Exp Allergy. 2005. 35:1135–1140.
14. Juhn YJ, Weaver A, Katusic S, Yunginger J. Mode of delivery at birth and development of asthma: a population-based cohort study. J Allergy Clin Immunol. 2005. 116:510–516.
15. Nafstad P, Magnus P, Jaakkola JJ. Risk of childhood asthma and allergic rhinitis in relation to pregnancy complications. J Allergy Clin Immunol. 2000. 106:867–873.
16. Crapo RO, Casaburi R, Coates AL, Enright PL, Hankinson JL, Irvin CG, MacIntyre NR, McKay RT, Wanger JS, Anderson SD, Cockcroft DW, Fish JE, Sterk PJ. Guidelines for methacholine and exercise challenge testing-1999. This official statement of the American Thoracic Society was adopted by the ATS Board of Directors, July 1999. Am J Respir Crit Care Med. 2000. 161:309–329.
17. Bousquet J, Khaltaev N, Cruz AA, Denburg J, Fokkens WJ, Togias A, Zuberbier T, Baena-Cagnani CE, Canonica GW, van Weel C, Agache I, Aït-Khaled N, Bachert C, Blaiss MS, Bonini S, Boulet LP, Bousquet PJ, Camargos P, Carlsen KH, Chen Y, Custovic A, Dahl R, Demoly P, Douagui H, Durham SR, van Wijk RG, Kalayci O, Kaliner MA, Kim YY, Kowalski ML, Kuna P, Le LT, Lemiere C, Li J, Lockey RF, Mavale-Manuel S, Meltzer EO, Mohammad Y, Mullol J, Naclerio R, O'Hehir RE, Ohta K, Ouedraogo S, Palkonen S, Papadopoulos N, Passalacqua G, Pawankar R, Popov TA, Rabe KF, Rosado-Pinto J, Scadding GK, Simons FE, Toskala E, Valovirta E, van Cauwenberge P, Wang DY, Wickman M, Yawn BP, Yorgancioglu A, Yusuf OM, Zar H, Annesi-Maesano I, Bateman ED, Ben Kheder A, Boakye DA, Bouchard J, Burney P, Busse WW, Chan-Yeung M, Chavannes NH, Chuchalin A, Dolen WK, Emuzyte R, Grouse L, Humbert M, Jackson C, Johnston SL, Keith PK, Kemp JP, Klossek JM, Larenas-Linnemann D, Lipworth B, Malo JL, Marshall GD, Naspitz C, Nekam K, Niggemann B, Nizankowska-Mogilnicka E, Okamoto Y, Orru MP, Potter P, Price D, Stoloff SW, Vandenplas O, Viegi G, Williams D; World Health Organization; GA(2)LEN; AllerGen. Allergic Rhinitis and its Impact on Asthma (ARIA) 2008 update (in collaboration with the World Health Organization, GA(2)LEN and AllerGen). Allergy. 2008. 63:Suppl 86. 8–160.
18. Hanifin JM, Rajka G. Diagnostic features of atopic dermatitis. Acta Derm Venereol. 1980. 92:44–47.
19. Maitra A, Sherriff A, Strachan D, Henderson J. Mode of delivery is not associated with asthma or atopy in childhood. Clin Exp Allergy. 2004. 34:1349–1355.
20. Hong SJ, Ahn KM, Lee SY, Kim KE. The Prevalences of Asthma and Allergic Diseases in Korean Children. Pediatr Allergy Respir Dis. 2008. 18:15–25.
21. Wylie BJ, Mirza FG. Cesarean delivery in the developing world. Clin Perinatol. 2008. 35:571–582. xii.
22. Hansen G, McIntire JJ, Yeung VP, Berry G, Thorbecke GJ, Chen L, DeKruyff RH, Umetsu DT. CD4(+) T helper cells engineered to produce latent TGF-beta1 reverse allergen-induced airway hyperreactivity and inflammation. J Clin Invest. 2000. 105:61–70.
23. Pessi T, Sutas Y, Hurme M, Isolauri E. Interleukin-10 generation in atopic children following oral Lactobacillus rhamnosus GG. Clin Exp Allergy. 2000. 30:1804–1808.
24. Thavagnanam S, Fleming J, Bromley A, Shields MD, Cardwell CR. A meta-analysis of the association between Caesarean section and childhood asthma. Clin Exp Allergy. 2008. 38:629–633.
25. Pistiner M, Gold DR, Abdulkerim H, Hoffman E, Celedon JC. Birth by cesarean section, allergic rhinitis, and allergic sensitization among children with a parental history of atopy. J Allergy Clin Immunol. 2008. 122:274–279.
26. Koplin J, Allen K, Gurrin L, Osborne N, Tang ML, Dharmage S. Is caesarean delivery associated with sensitization to food allergens and IgE-mediated food allergy: a systematic review. Pediatr Allergy Immunol. 2008. 19:682–687.
27. McKeever TM, Lewis SA, Smith C, Hubbard R. Mode of delivery and risk of developing allergic disease. J Allergy Clin Immunol. 2002. 109:800–802.