Skip to main content
Erschienen in: BMC Pediatrics 1/2019

Open Access 01.12.2019 | Research article

Prenatal and neonatal factors involved in the development of childhood allergic diseases in Guangzhou primary and middle school students

verfasst von: Bolan Yu, Lijuan Dai, Juanjuan Chen, Wen Sun, Jingsi Chen, Lili Du, Nali Deng, Dunjin Chen

Erschienen in: BMC Pediatrics | Ausgabe 1/2019

Abstract

Background

Allergic diseases, such as asthma, dermatitis, rhinitis, and eczema, are highly prevalent in Chinese school children. Environmental factors, including air pollution and automobile exhaust, play an important role in the etiology of these diseases. However, prenatal and neonatal factors, such as gender, maternal diseases during pregnancy, and premature birth, may also be associated with allergic disease occurrence. The objective of this study was to explore prenatal and neonatal factors that are involved in the development of allergic diseases among primary and middle school students in Guangzhou, China.

Methods

A cross-sectional survey was launched by the Health Promotion Centre for Primary and Secondary Schools of the Guangzhou Municipality in October 2017. All primary and middle school students in Guangzhou were notified to participate in the questionnaire online under the direction of their parents. The results of the physical examination were reported by the schools’ medical department. The results of the questionnaire were collected and analyzed by the researchers. The prevalence of asthma, allergic rhinitis, allergic dermatitis, and eczema was identified.

Results

Based on reported 183,449 questionnaires and medical records, the data indicate that the sex, birth weight, neonatal feeding type, delivery mode, and students’ father smoking status were significantly associated with the prevalence of all four allergic diseases in primary and middle school children. In further stratified analyses of the children with normal birth weight (2500–4000 g) and without any maternal diseases during pregnancy, the factors of male sex, high birth weight, cesarean delivery, and father smoking status all increased the risk of asthma, dermatitis, rhinitis, and eczema. Also, unlike exclusive breastfeeding, breast plus formula feeding increased these risks, but pure formula feeding had the opposite effect.

Conclusion

Prenatal and neonatal factors, including male sex, high birth weight, cesarean delivery, only child, and father smoking status are associated with the risks of allergic diseases in school children.
Hinweise

Supplementary information

Supplementary information accompanies this paper at https://​doi.​org/​10.​1186/​s12887-019-1865-0.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
ASAS
Aberdeen Schools Asthma Survey
CI
Confidence Interval
CS
Caesarean Section
DOHaD
Developmental Origins of Health and Disease
HR
Hazard Ratio
IRR
Incidence Rate Ratios
OR
Odd Ratios
SD
Standard Deviation
SMS
Short Messaging Service

Background

Allergic diseases, such as asthma, dermatitis, rhinitis, and eczema, have become a severe clinical and public health problem, both worldwide and in the Guangzhou area. Asthma is a chronic inflammation of the airways that is often accompanied by extensive and variable airflow obstruction [1]. Allergic dermatitis is an inflammatory reaction that occurs at a contact site or part of the skin or mucous membrane after a single or multiple exposures to an exogenous substance [2]. Allergic rhinitis is characterized by at least two nasal symptoms: rhinorrhoea, blockage, sneezing or itching [3]. Eczema is a chronic, relapsing illness characterized by skin lesions [4]. These four allergic diseases are highly prevalent in Chinese school children, and the prevalence rates of asthma, allergic dermatitis, allergic rhinitis, and eczema are about 10.8, 0.5, 10.8, and 4.8%–15.8%, respectively [58].
Environmental factors, such as air pollution and automobile exhaust, play an important role in the etiology of these four allergic diseases. Tobacco smoke, due to parental smoking, is considered a major indoor pollutant for children with allergic diseases [912]. In addition, prenatal and neonatal factors, such as gender, maternal diseases during pregnancy, and premature birth, may be associated with allergic disease occurrence. It is known that the prevalence of asthma in adult women has increased compared with men [13, 14], and the prevalence of allergic dermatitis is significantly higher in girls than in boys [15]. Compared with full-term born children, premature children have a higher risk of allergic diseases, such as severe asthma and atopic dermatitis [1618]. Meta-analysis has shown that low birth weight significantly increased the risk of asthma in children [19]. Breastfeeding is considered a protective measure against the development of allergic diseases, at least for neonates [2023]. In addition, cesarean section (CS) and instrumental delivery might render the baby more susceptible to allergic diseases, most likely because it disrupts the mother-to-newborn transmission of microbes [2428]. Maternal diseases during pregnancy are known to have a negative effect on fetal development. Moreover, maternal hypertension and thyroid dysfunction during pregnancy have been associated with a high prevalence of allergic diseases in the offspring [2931]. Thus, prenatal and neonatal factors have a significant impact on the development of childhood diseases; however, further research is warranted in order to fully understand how these factors influence allergic diseases in children [32].
The purpose of our study was to systematically address the effects of various prenatal and neonatal factors on the development of allergic diseases in primary and secondary school students in Guangzhou, China. Based on a large population survey in Guangzhou primary and middle school, our study may provide insights into, and evidence of, the association between prenatal and neonatal factors and childhood allergic diseases in Southern area of China.

Methods

Data source

This study was approved by the ethics committee of The Third Affiliated Hospital of Guangzhou Medical University [2017(No.128)], and studies involving human subjects were conducted in accordance with the Declaration of Helsinki guidelines.
A cross-sectional survey design was applied, and all primary and middle schools in Guangzhou, China were invited to participate. The health survey was launched and supervised by the Health Promotion Centre for Primary and Secondary Schools of the Guangzhou Municipality, which is responsible for monitoring the health status of students from primary and secondary schools in Guangzhou. All primary and secondary school students in Guangzhou were notified by their school to participate in the survey in October 2017.
This health survey required participated children and parents jointly filled out the online questionnaire according to their own situation and directly submitted the questionnaire (see the Additional file 1). The questionnaire collected comprehensive data regarding the birth, and relevant prenatal, neonatal, and family information regarding the child, including birth weight, sex, neonatal feeding, delivery, delivery date, maternal diseases during pregnancy, parents’ education, parental smoking, and average household monthly income per person. At the time of the questionnaire or ever diagnosed diseases including asthma, dermatitis, rhinitis, and eczema were self-reported by the participants according to their out-patient clinical records.
According to the 2017 Guangzhou Education Statistics Handbook, the number of primary and secondary school students in 2017 was 1,514,122. The survey covered 11 administrative districts, including 991 schools. The first page of the questionnaire stated that the results of the health questionnaire would be used for health research.

Statistical methods

The characteristics of the participants were reported as mean (SD, standard deviation) for continuous variables and frequency (proportion) for categorical variables. The prevalence (95% confidence interval (CI)) of allergic diseases was estimated by the categories of the participants’ characteristics. The prevalence of categories was compared using logistic regression. Multiple logistic regression analysis was performed in order to detect potential risk factors of allergic diseases. The participants who were singletons with normal birth weights (2500–4000 g) and whose mother had no diseases during pregnancy were included in the regression analysis. Questionnaires with missing data were not used for analysis. Variables with P < 0.05 in simple regression analysis were included in the multiple regression model. All P values were based on two-sided tests (P < 0.05 was considered significant). Statistical analyses were performed using SAS version 9.4 (SAS Institute Inc., Cary, NC, USA).

Results

The health survey was launched and supervised by the Health Promotion Centre for Primary and Secondary Schools of the Guangzhou Municipality. All primary and secondary school students in Guangzhou City (1479 schools and 1,514,122 students) were invited to participate in this study. There were 991 schools, and a total of 253,301 students participated in the survey. Participants were from 11 districts within Guangzhou city, including Liwan, Yuexiu, Haizhu, Tianhe, Baiyun, Huangpu, Panyu, Huadu, Nansha, Chonghua, and Zengcheng. Their ages ranged from 6 to 18 years old. The final collected questionnaire number was 253,301, and the number of questionnaires with missing data was 69,852. The response rate was 16.7%.
Among the students participating in the study, 3449 (1.37%), 13,819 (5.50%), 10,260 (4.08%), and 11,484 (4.63%) experienced asthma, allergic dermatitis, allergic rhinitis, and eczema, respectively. The mean (standard deviation, SD) of birth weight students was 2990 (420) g. Males accounted for 53.7%. The percentage of singletons participating was 38.6%. The three types of neonatal feeding — breastfeeding, breast and formula feeding, and formula feeding — accounted for 44.0, 38.9, and 17.1%, respectively. Vaginal delivery accounted for 58.8% and CS accounted 41.2% of the completed surveys. According to the results, 27.6% of the children were full-term born, 24.3% were post-term born, and 48.2% were preterm born. Only 12.6% reported major maternal diseases during pregnancy. The prevalence of smoking by the father was 50.7%, with 7.95% of whom were quit > 1 year before the survey, 2.34% of whom quit < 1 year before the survey, and 40.50% as current smokers. The prevalence of smoking among the mothers was 0.9%, with 99.1% reporting as never having smoked. (Table 1).
Table 1
Characteristics of participants
Characteristics
All
Non-case group*
Case group*
P-value§
Total, n (%)
183,449 (100)
158,305 (86.3)
25,144 (13.7)
/
Grade, n (%)
   
< 0.001†
 1–6
136,771 (74.6)
117,450 (74.2)
19,321 (76.8)
 
 7–9
33,013 (18.0)
29,014 (18.3)
3999 (15.9)
 
 10–12
13,665 (7.45)
11,841 (7.48)
1824 (7.25)
 
Age, Years, n (%)#
   
< 0.001†
 6–10
114,026 (62.2)
97,603 (61.7)
16,423 (65.3)
 
 11–15
59,374 (32.4)
51,961 (32.8)
7413 (29.5)
 
  > 15
10,049 (5.48)
8741 (5.52)
1308 (5.20)
 
 Mean (SD)
9.94 (2.99)
9.97 (3.00)
9.76 (2.96)
< 0.001¶
Sex, n (%)
 Male
98,565 (53.7)
83,995 (53.1)
14,570 (58.0)
< 0.001‡
 Female
84,884 (46.3)
74,310 (46.9)
10,574 (42.1)
 
 Birth weight, kg, Mean (SD)
2.99 (0.42)
2.98 (0.42)
3.02 (0.43)
< 0.001¶
Neonatal feeding, n (%)
   
< 0.001‡
 Breast feeding
80,718 (44.0)
70,723 (44.7)
9995 (39.8)
 
 Breast+ formula feeding
71,363 (38.9)
60,184 (38.0)
11,179 (44.5)
 
 Formula feeding
31,368 (17.1)
27,398 (17.3)
3970 (15.8)
 
Delivery, n (%)
   
< 0.001‡
 Vaginal delivery
107,830 (58.8)
94,232 (59.5)
13,598 (54.1)
 
 Cesarean
75,619 (41.2)
64,073 (40.5)
11,546 (45.9)
 
Delivery date, n (%)
   
< 0.001‡
 On the due date
50,595 (27.6)
45,627 (28.8)
4968 (19.8)
 
 Overdue
44,520 (24.3)
37,855 (23.9)
6665 (26.5)
 
 Before the due date
88,334 (48.2)
74,823 (47.3)
13,511 (53.7)
 
Diseases in pregnancy, n (%)
 Hypertension
3005 (1.64)
2472 (1.56)
533 (2.12)
< 0.001‡
 Diabetes
4290 (2.34)
3329 (2.10)
961 (3.82)
< 0.001‡
 Intrahepatic cholestasis
486 (0.26)
383 (0.24)
103 (0.41)
< 0.001‡
 Hypothyroidism
590 (0.32)
470 (0.30)
120 (0.48)
< 0.001‡
 Hyperthyroidism
760 (0.41)
626 (0.40)
134 (0.53)
0.002‡
 Anemia
13,515 (7.37)
10,701 (6.76)
2814 (11.2)
< 0.001‡
 Viral hepatitis
1950 (1.06)
1604 (1.01)
346 (1.38)
< 0.001‡
 Other
1331 (0.73)
968 (0.61)
363 (1.44)
< 0.001‡
 Any disease above
23,175 (12.6)
18,434 (11.6)
4741 (18.9)
< 0.001‡
 Only child, n (%)
70,832 (38.6)
59,201 (37.4)
11,631 (46.3)
< 0.001‡
 One or both parents’ education> 12 years, n (%)
133,304 (72.7)
113,317 (71.6)
19,987 (79.5)
< 0.001‡
Father smoking, n (%)
   
0.129†
 Never smoked
90,370 (49.3)
78,172 (49.4)
12,198 (48.5)
 
 Quit for > 1 year
14,584 (7.95)
12,410 (7.84)
2174 (8.65)
 
 Quit for < 1 year
4291 (2.34)
3698 (2.34)
593 (2.36)
 
 Current smoking
74,204 (40.5)
64,025 (40.4)
10,179 (40.5)
 
Mother smoking, n (%)
   
0.519†
 Never smoked
181,814 (99.1)
156,903 (99.1)
24,911 (99.1)
 
 Quit for > 1 year
672 (0.37)
575 (0.36)
97 (0.39)
 
 Quit for < 1 year
218 (0.12)
189 (0.12)
29 (0.12)
 
 Current smoking
745 (0.41)
638 (0.40)
107 (0.43)
 
Average Household monthly income per person, US$, n (%)
   
< 0.001†
  < 735
61,248 (33.4)
54,362 (34.3)
6886 (27.4)
 
 735–1764
74,842 (40.8)
64,471 (40.7)
10,371 (41.3)
 
  > =1764
47,359 (25.8)
39,472 (24.9)
7887 (31.4)
 
SD: Standard deviation; 1USAdollar = 6.80RMB
#: The mean age of school grade 1 is six years old
* Case group included children who had allergic asthma, allergic dermatitis, allergic rhinitis and eczema, and children without above cases were included in the non-case group
§ P value was for comparing the differences between case group and non-case group
† Ordinal logistic regression was used for the comparison
‡ Chi-squared test was used for the comparison
¶ Two sample t test was used for the comparison
The prevalence (95% confidence interval, CI) of asthma, allergic dermatitis, allergic rhinitis, and eczema was higher (P < 0.001) in boys than girls: 1.94% (1.85, 2.03%) vs. 1.09% (1.02, 1.16%), 6.80% (6.64, 6.96%) vs. 5.95% (5.79, 6.11%), 4.50% (4.37, 4.63%) vs. 3.74% (3.61, 3.87%), and 5.51% (5.36, 5.65%) vs. 4.71% (4.57, 4.85%), respectively (Table 2). The prevalence (95% CI) of asthma in neonatal babies being breastfed only was lower [1.31% (1.24, 1.38%)] than that in those being breastfed and formula fed together (mixed feeding) [1.79% (1.69, 1.88%), P < 0.001], and lower than that in those being formula fed only [1.61% (1.47, 1.75%), P < 0.001]. The same direction of differences in the prevalence (95% CI) of allergic dermatitis, allergic rhinitis, and eczema was found comparing breastfeeding only [5.61% (5.46, 5.77%), 3.61% (3.48, 3.74%), 4.83% (4.68, 4.97%), respectively] with mixed feeding [7.69% (7.49, 7.88%), 4.78% (4.63, 4.94%), 5.71% (5.54, 5.88%), respectively, all P < 0.001] and formula feeding only [5.52% (5.27, 5.78%), 4.11% (3.89, 4.33%), 4.65% (4.42, 4.88%), respectively, all P < 0.001]. The prevalence (95% CI) of asthma [1.88% (1.78, 1.98%)], allergic dermatitis [7.27% (7.08, 7.45%)], allergic rhinitis [4.77% (4.62, 4.92%)], and eczema [5.47% (5.31, 5.63%)] was higher (P < 0.001) in students born by CS than that in students born by vaginal delivery [1.31% (1.24, 1.38%), 5.80% (5.66, 5.94%), 3.72% (3.60, 3.83%), 4.91% (4.78, 5.04%), respectively, all P < 0.001]. Students whose mother had maternal pregnancy diseases had higher (all P < 0.001) prevalence of allergic diseases than students whose mother had no maternal pregnancy disease (Table 2). Students who were singletons had higher prevalence (95% CI) of asthma [1.95% (1.84, 2.05%)], allergic dermatitis [7.90% (7.70, 8.10%)], allergic rhinitis [5.08% (4.91, 5.24%)], and eczema [6.00% (5.83, 6.18%)] than students who had siblings [1.29% (1.23, 1.36%), 5.47% (5.33, 5.60%), 3.57% (3.46, 3.68%), 4.59% (4.47, 4.72%), respectively, all P < 0.001].
Table 2
Prevalence (95% CI) of allergic diseases by categories of the participants’ characteristics (N = 183,449) *#
 
Allergic asthma§
Allergic dermatitis†
Allergic rhinitis‡
Eczema¶
All
1.55 (1.49, 1.60)
6.41 (6.29, 6.52)
4.15 (4.06, 4.24)
5.14 (5.04, 5.24)
Grade
 1–6
1.47 (1.41, 1.53)
6.94 (6.80, 7.07)
4.19 (4.08, 4.30)
5.21 (5.09, 5.33)
 7–9
1.70 (1.56, 1.83)**
4.68 (4.45, 4.91)***
4.02 (3.81, 4.23)
4.71 (4.48, 4.94)***
 10–12
1.96 (1.72, 2.19)***
5.27 (4.90,5.65)***
4.08 (3.75, 4.41)
5.43 (5.05, 5.81)
Age, Years
 6–10
1.45 (1.38, 1.52)
7.25 (7.10, 7.40)
4.20 (4.09, 4.32)
5.28 (5.15, 5.41)
 11–15
1.66 (1.56, 1.76)***
5.06 (4.88, 5.23)***
4.06 (3.91, 4.22)
4.83 (4.66, 5.01)***
  > 15
1.99 (1.72, 2.26)***
4.81 (4.39, 5.23)***
4.09 (3.70, 4.48)
5.32 (4.88, 5.76)
Sex
 Female
1.09 (1.02, 1.16)
5.95 (5.79, 6.11)
3.74 (3.61, 3.87)
4.71 (4.57, 4.85)
 Male
1.94 (1.85, 2.03)***
6.80 (6.64, 6.96)***
4.50 (4.37, 4.63)***
5.51 (5.36, 5.65)***
Neonatal feeding
 Breast feeding
1.31 (1.23, 1.39)
5.61 (5.46, 5.77)
3.61 (3.48, 3.74)
4.83 (4.68, 4.97)
 Breast + formula feeding
1.79 (1.69, 1.88)***
7.69 (7.49, 7.88)***
4.78 (4.63, 4.94)***
5.71 (5.54, 5.88)***
 Formula feeding
1.61 (1.47, 1.75)***
5.52 (5.27, 5.78)
4.11 (3.89, 4.33)***
4.65 (4.42, 4.88)
Delivery
 Vaginal delivery
1.31 (1.24, 1.38)
5.80 (5.66, 5.94)
3.72 (3.60, 3.83)
4.91 (4.78, 5.04)
 Cesarean
1.88 (1.78, 1.98)***
7.27 (7.08, 7.45)***
4.77 (4.62, 4.92)***
5.47 (5.31, 5.63)***
Diseases in pregnancy
Hypertension
 No
1.52 (1.46, 1.58)
6.36 (6.25, 6.47)
4.13 (4.04, 4.22)
5.11 (5.01, 5.21)
 Yes
3.17 (2.54, 3.79)***
9.10 (8.07, 10.1)***
5.59 (4.77, 6.42)***
6.87 (5.97, 7.78)***
Diabetes
 No
1.50 (1.44, 1.56)
6.26 (6.15, 6.37)
4.08 (3.99, 4.17)
5.09 (4.99, 5.19)
 Yes
3.48 (2.93, 4.02)***
12.5 (11.5, 13.5)***
7.12 (6.35, 7.90)***
7.25 (6.47, 8.02)***
Intrahepatic cholestasis
 No
1.54 (1.48, 1.59)
6.39 (6.28, 6.50)
4.14 (4.05, 4.23)
5.13 (5.03, 5.23)
 Yes
4.54 (2.68, 6.39)***
11.3 (8.52, 14.2)***
9.05 (6.50, 11.6)***
9.11 (6.54, 11.7)***
Hypothyroidism
 No
1.54 (1.48, 1.59)
6.39 (6.28, 6.50)
4.14 (4.05, 4.23)
5.13 (5.03, 5.23)
 Yes
4.76 (3.04, 6.48)***
10.7 (8.23, 13.2)***
8.32 (6.09, 10.6)***
8.72 (6.43, 11.0)***
Hyperthyroidism
 No
1.53 (1.48, 1.59)
6.40 (6.29, 6.51)
4.14 (4.05, 4.23)
5.13 (5.03, 5.23)
 Yes
4.61 (3.12, 6.10)***
8.30 (6.34, 10.3)*
7.51 (5.63, 9.38)***
6.94 (5.12, 8.76)*
Anemia
 No
1.50 (1.45, 1.56)
6.06 (5.95, 6.18)
3.94 (3.84, 4.03)
4.95 (4.85, 5.06)
 Yes
2.08 (1.84, 2.32)***
10.7 (10.2, 11.2)***
6.87 (6.45, 7.30)***
7.49 (7.04, 7.93)***
Viral hepatitis
 No
1.53 (1.48, 1.59)
6.38 (6.27, 6.49)
4.13 (4.04, 4.22)
5.11 (5.01, 5.22)
 Yes
2.77 (2.04, 3.50)***
8.83 (7.57, 10.1)***
6.11 (5.05, 7.17)***
7.33 (6.17, 8.50)***
Other
 No
1.53 (1.47, 1.58)
6.35 (6.24, 6.46)
4.10 (4.01, 4.19)
5.11 (5.01, 5.21)
 Yes
4.22 (3.14, 5.30)***
13.8 (12.0, 15.7)***
11.3 (9.59, 13.0)***
9.12 (7.56, 10.7)***
Any disease above
 No
1.42 (1.36, 1.48)
5.82 (5.71, 5.94)
3.79 (3.70, 3.88)
4.83 (4.73, 4.94)
 Yes
2.43 (2.23, 2.63)***
10.4 (10.0, 10.8)***
6.65 (6.33, 6.97)***
7.26 (6.93, 7.60)***
Only child
 No
1.29 (1.23, 1.36)
5.47 (5.33, 5.60)
3.57 (3.46, 3.68)
4.59 (4.47, 4.72)
 Yes
1.95 (1.84, 2.05)***
7.90 (7.70, 8.10)***
5.08 (4.91, 5.24)***
6.00 (5.83, 6.18)***
Father smoking
 Never smoked
1.56 (1.47, 1.64)
6.45 (6.29, 6.61)
3.99 (3.87, 4.12)
5.00 (4.86, 5.14)
 Quit for > 1 year
1.86 (1.64, 2.08)**
6.61 (6.21, 7.02)
4.58 (4.24, 4.92)***
5.66 (5.28, 6.04)***
 Quit for < 1 year
1.63 (1.25, 2.01)
6.11 (5.40, 6.83)
4.01 (3.43, 4.60)
5.43 (4.75, 6.11)
 Current smoking
1.47 (1.38, 1.56)
6.33 (6.15, 6.50)
4.27 (4.12, 4.41)**
5.19 (5.03, 5.35)
CI Confidence Interval
*: prevalence (95% CI) (* P < 0.05, ** P < 0.01 and *** P < 0.001 indicating the significance of comparing each of other categories with the first category as the reference group
#: Two proportion Z test was used for comparing prevalence of allergic disease in categories of the participants’ characteristics with the first category as the reference group
§: 2,832/183,162 (1.55%), 287 missing values;
†: 11,731/183,142 (6.41%), 307 missing values;
‡: 7,607/183,238 (4.15%), 211 missing values;
¶: 9,352/181,997 (5.14%), 1452 missing values
Table 3 summarizes the results of four multiple logistic regression models for asthma, allergic dermatitis, allergic rhinitis, and eczema (N = 149,726). The participants in the model were singletons with normal birth weight (2500–4000 g) and whose mother had no diseases during pregnancy, as both birth weight and maternal pregnancy diseases are known factors that influence fetal growth and long-term diseases. With the age of students, the risk of allergic asthma [OR (95% CI): 1.04 (1.03, 1.06), P < 0.001] increased, while the risk of allergic dermatitis [OR (95% CI: 0.93 (0.93, 0.94, P < 0.001)] and eczema [OR (95% CI: 0.99 (0.98, 0.99), P < 0.001] decreased. A higher risk of asthma, allergic dermatitis, allergic rhinitis, and eczema was detected in males compared with females [OR (95% CI): 1.78 ((1.62, 1.95), 1.09 (1.04, 1.14), 1.18 (1.12, 1.24), and 1.14 (1.09, 1.20), respectively, all P < 0.001], in students with greater weight [OR (95% CI): 1.29 (1.15, 1.44), 1.28 (1.21, 1.36), 1.22 (1.14, 1.31), and 1.09 (1.02, 1.16), respectively, all P < 0.001], and also in the students born by CS compared to students born by vaginal delivery [OR (95% CI): 1.32 (1.21, 1.44), 1.17 (1.12, 1.22), 1.25 (1.18, 1.32), and 1.07 (1.01, 1.12) respectively, all P < 0.001]. Compared to breastfeeding only, the risk of asthma, allergic dermatitis, allergic rhinitis, and eczema was higher for mixed feeding [OR (95% CI): 1.27 (1.16. 1.40), 1.32 (1.26, 1.38), 1.35 (1.27, 1.43), and 1.16 (1.11, 1.23), respectively, all P < 0.001]. We found that the smoking status of the students’ father was associated with the prevalence of allergic diseases as well, as students whose father quitted for > 1 year had a higher risk of asthma, allergic rhinitis, and eczema [OR (95% CI): 1.23 (1.06, 1.43), 1.12 (1.02, 1.24), and 1.19 (1.09, 1.30), respectively, all P < 0.001].
Table 3
Multiple Logistic regression model of potential risk factors of allergic diseases among participants (OR (95% CI) and P value were presented) (N = 149,726) *
Variable#
Allergic asthma
Allergic dermatitis
Allergic rhinitis
Eczema
Age, Year
1.04 (1.03, 1.06) < 0.001
0.93 (0.925, 0.94) < 0.001
/
0.99 (0.98, 0.995) 0.002
Male
1.78 (1.62, 1.95) < 0.001
1.09 (1.04, 1.14) < 0.001
1.18 (1.12, 1.24) < 0.001
1.14 (1.09, 1.20) < 0.001
Birth weight, kg
1.29 (1.15, 1.44) < 0.001
1.28 (1.21, 1.36) < 0.001
1.22 (1.14, 1.31) < 0.001
1.09 (1.02, 1.16) 0.008
Neonatal feeding
 Breast feeding
Reference
Reference
Reference
Reference
 Breast+ formula feeding
1.27 (1.16, 1.40) < 0.001
1.32 (1.26, 1.38) < 0.001
1.35 (1.27, 1.43) < 0.001
1.16 (1.11, 1.23) < 0.001
 Formula feeding
1.08 (0.95, 1.23) 0.230
0.89 (0.83, 0.95) < 0.001
1.11 (1.02, 1.20) 0.014
0.91 (0.84, 0.97) 0.007
Delivery
 Vaginal delivery
Reference
Reference
Reference
Reference
 Cesarean
1.32 (1.21, 1.44) < 0.001
1.17 (1.12, 1.22) < 0.001
1.25 (1.18, 1.32) < 0.001
1.07 (1.01, 1.12) 0.012
  Only child
1.32 (1.21, 1.44) 0.002
1.45 (1.38, 1.51) < 0.001
/
1.30 (1.24, 1.37) < 0.001
Father smoking
 Never smoked
Reference
/
Reference
Reference
 Quit for > 1 year
1.23 (1.06, 1.43) 0.006
/
1.12 (1.02, 1.24) 0.020
1.19 (1.09, 1.30) < 0.001
 Quit for < 1 year
1.10 (0.84, 1.45) 0.486
/
0.94 (0.78, 1.13) 0.520
1.11 (0.95, 1.29) 0.189
 Current smoking
0.91 (0.83, 1.00) 0.038
/
1.06 (1.00, 1.12) 0.039
1.07 (1.02, 1.13) 0.007
OR Odds Ratio, CI Confidence Interval
*: The multiple Logistic regression was conducted among participants who were singletons with normal birth weight (2.5-4 kg) and whose mother had no pregnancy disorder during pregnancy
#: All variables in the Table 1 were included in the simple regression. Variables with P < 0.05 in the simple regression analysis were included in the multiple regression model. The results of simple regression analysis were not listed in the table

Discussion

According to Developmental Origins of Health and Disease (DOHaD) theory, the development of childhood diseases may be affected by factors in prenatal and neonatal life [32, 33]. Several epidemiological studies have revealed that prenatal and neonatal factors, such as the delivery mode, feeding type, and pregnancy diseases, may alter the risks of childhood allergic diseases, including asthma, dermatitis, rhinitis, and eczema [9, 16, 3438]. However, most of these studies have been conducted in Western countries, and further epidemiological studies covering different areas and populations are warranted. In the Guangzhou area of southern China, allergic diseases are prevalent in school children. Although environmental factors, such as indoor and outdoor smoke, have been widely discussed, prenatal and neonatal factors are largely omitted. Therefore, a retrospective survey in all Guangzhou primary and middle school students was launched to study the association between prenatal and neonatal factors and allergic disease prevalence in school students 6–17 years old.
Based on 183,449 reported questionnaires and medical records, this cross-sectional survey study revealed that a parent-reported history of asthma, dermatitis, rhinitis, and eczema was present in 1.55% (1.49, 1.60%), 6.41% (6.29, 6.52%), 4.15% (4.06, 4.24%), and 5.14% (5.04, 5.24%) of school children, respectively (Table 2). In this study, the prevalence of asthma and rhinitis was lower, while the prevalence of dermatitis and eczema was higher than the reported prevalence in China [58]. These differences may be due to the lower air pollution in the Guangzhou area relative to northern China, and to the wet and hot climate of this area, which might cause more risks of skin diseases.
In our study, epidemiological data supported that the sex, birth weight, neonatal feeding type, delivery mode, and the smoking status of the father were significantly associated with the prevalence of all four allergic diseases. In further stratified analyses of children with normal birth weight without any maternal pregnancy diseases, prenatal and neonatal factors, including male sex, high birth weight, cesarean delivery, only child, and smoking status of the father, all increased the risks of asthma, dermatitis, rhinitis, and eczema in primary and middle school children. Unlike breastfeeding alone, breast plus formula feeding increased the risk of allergic diseases, but pure formula feeding decreased the risks.
Previous studies have reported that the prevalence of four allergic diseases — asthma, dermatitis, rhinitis, and eczema — has gender disparity within different populations [13]. For instance, asthma prevalence and mortality are higher among adult women than men overall; however, the prevalence is higher among boys than girls 0–14 years of age. The reasons for the gender difference are not thoroughly understood, but have been linked to gender-specific responses to environmental or occupational exposures involving immunological and hormonal factors [13, 14]. Our study also supported that boys have a higher risk of asthma, dermatitis, rhinitis, and eczema in all age groups relative to girls. In the Aberdeen Schools Asthma Survey (ASAS) in Scotland, one of the longest-running pediatric epidemiology studies in the world, males were reported to have a higher risk of asthma [9]. A national register study in Finland assessed 1,018,302 children between 1991 and 2008 and found that the male sex predicted asthma medication in preterm children [16]. In Norwegian registries with prospectively collected data, the male gender showed an increased asthma risk [17]. In addition, aging increases the incidence of allergic diseases from our results. In the Scotland ASAS study, the odds of a parent-reported lifetime of asthma increased with age [9], which is consistent with our results.
Smoking is a common environmental factor that is a health hazard. Almost all epidemiologic studies reported, thus far, support the negative impact of environmental tobacco smoke or parental cigarette smoking on pediatric allergic diseases, such as asthma. In the Scotland ASAS study, parental smoking increased the risk of asthma and wheezing, but not eczema and hay fever [9]. In Finland, parental smoking was highly associated with childhood asthma [39], and maternal smoking predicted asthma medication in preterm children [16]. In a Japanese study of 36,888 surveyed, maternal indoor smoking significantly increased the risk of asthma development in children, and paternal smoking slightly increased the prevalence of asthma development in children, but was not statistically significant [12]. In the city of Guangzhou in China, the situation differs from other areas. First, the male smoking rate is reported to be as high as 48.4%, and most began smoking as teenagers. Although many fathers quit smoking after childbirth, the potential effects of smoking still exist; therefore, previous smoking status should be considered. Second, female smoking is rare, to such an extent that in this study 99.2% of the mothers never smoked; therefore, unlike other countries, maternal smoking in China may not be a significant factor for consideration. Thus, the impact of indoor smoke hazards may decrease, while outdoor environmental hazard exposure may increase. Our study supports that the smoking status of the father, particularly smoking vs. non-smoking, influences allergic diseases in children, which may reflect the epigenetic alterations during early lifetime.
Preterm birth and low birth weight are considered risk factors for major allergic diseases. In Japan, a recent cross-sectional study found no significant associations between low birth weight, preterm birth, and prevalence of wheezing, asthma, or eczema [11]. A meta-analysis of 13 cohort studies and 1,105,703 subjects found that the overall pooled risk ratio of asthma in low birth weight children was 1.162, and low birth weight significantly increased the risk of childhood asthma [19]. In Norwegian registries with prospectively collected data, preterm birth was associated with an increased risk of severe asthma and a decreased risk of severe atopic dermatitis [17]. Data from 700 families in the Netherlands supported that children with low birth weight tended to have a lower risk of any allergy, albeit not significant, and prematurity was a risk factor for asthma at six years of age [40]. Our study was retrospective, and parents only reported the situation of delivery as due date, overdue date, or before the due date, broad categories that can be correctly remembered by them. As preterm delivery is commonly believed to be a risk factor for allergic diseases, we only studied the children who had normal birth weight (2500–4000 g); hence, we excluded the preterm and overdue date children. Interestingly, in the normal birth weight children, the risk of allergies was adversely linked with birth weight, as higher birth weights had a higher risk for diseases.
Pregnancy diseases in mothers, including maternally related diseases, such as hyperemesis, hypertension, and preeclampsia, and uterus-related complications, such as antepartum hemorrhage, preterm contractions, and insufficient placenta, affect the growth of the fetus in the uterus and probably also the overall long-term health. In a population-based cohort study in Denmark involving 5,95,669 children, the incidence rate ratios of asthma were 1.1 and 1.12 for children born to mothers with hypothyroidism that was diagnosed before or after delivery. The highest risk was observed among children born to mothers with hypothyroidism diagnosed before delivery who did not receive thyroid hormone treatment during pregnancy [31]. A population-based four-year cohort study involving 2531 children born in Norway found only uterus-related, but not other pregnancy-related complications, increased the risk of bronchial obstruction, asthma, and allergic rhinitis [30]. In the Avon Longitudinal Study, hypertension before pregnancy was positively associated with wheezing and asthma [29]. Our data support that all pregnancy diseases, including preeclampsia and diabetes, increased the risk of allergic diseases in children.
The mode of delivery may affect outcomes, such as asthma and allergic disease, in children many years later. Recent meta-analyses have reported a 20% increase in the subsequent risk of asthma in children delivered by CS and a moderate risk increase for allergic rhinitis and asthma. Recent studies have reported that children born by CS have an increased risk of asthma, whereas others found no such association [10].. In a cross-sectional study of 672 children nested in a birth cohort evaluated at 6 years of age in Brazil, the parental history of asthma was an effect modifier in the association between CS, chronic rhinitis, and allergic rhinitis. CS increases the risk of chronic rhinitis and allergic rhinitis in children at six years of age that have a parental history of asthma [26]. Further investigations on the long-term effects of emergency and elective CS may include a systematic survey of all modes of delivery [12]. In a population-representative prospective birth cohort of 8327 Chinese children in Hong Kong, it was found that delivery by CS accounted for 27% of all births and was not clearly associated with hospitalizations for asthma or other wheezing disorders at 12 years of age compared to vaginal delivery. Similarly, there were no clear associations at 2 years of age or six years of age [41]. Our findings suggest an association between delivery by CS and childhood allergic disorders. However, if CS is stratified into an emergency CS and elected CS, the associations may vary and may not be biologically mediated.
Feeding type is another controversial factor for asthma. It is believed that breastfeeding is protective against allergic diseases, at least in infants. However, effects in older children, such as school students, are controversial. Exclusive breastfeeding for at least three months reduces the risk of atopic dermatitis, at least during infancy. No clear risk reduction was evident, however, for asthma, allergic rhinitis, positive allergen skin tests, or food allergies [20]. A systematic review suggested that a longer duration of breastfeeding (vs. a shorter duration) was associated with a reduced risk of asthma for children (5–18 years), particularly in medium- and low-income countries, and with a reduced risk of allergic rhinitis in children ≤5 years [21]. Our data show that breast plus formula feeding increased the risks of allergic diseases compared to exclusive breast milk, but pure formula feeding decreased the risks. One reason for this is that in the Guangzhou area, the formula is likely to be afforded by families with high incomes; therefore, formula feeding can be linked with socioeconomic status.

Conclusion

Risk factors for allergic diseases have been explored for many years as the growing prevalence of allergic diseases in the world. This study collected the data from 183,449 surveys for investigation. The results indicate that, in school children without any maternal complications during pregnancy, prenatal and neonatal factors, including male sex, high birth weight, cesarean delivery, only child, and father’s smoking status all increased the risk of asthma, dermatitis, rhinitis, and eczema, but exclusive formula feeding decreased the risk. Therefore, this study reported the major prenatal and neonatal factors associated with allergic diseases in school children in the Southern area of China. Although the results overlap with other studies, it is still important that there is a very large population from a specific area participated in the study. Therefore, this study provides strong evidence to support known risk factors for allergic diseases in school children.

Supplementary information

Supplementary information accompanies this paper at https://​doi.​org/​10.​1186/​s12887-019-1865-0.

Acknowledgements

We thank LetPub (www.​letpub.​com) for its linguistic assistance during the preparation of this manuscript.
Not applicable.
This study was approved by the ethics committee of The Third Affiliated Hospital of Guangzhou Medical University [2017(No.128)], and all the procedures have been approved by the ethics committee. Consent to participate was collected from the parents of school students who were informed about this study at the parent-teacher conference, using posters and SMS notification. Because this study was online health survey, only verbal consents were obtained.

Competing interests

The authors declare that they have no competing interests.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Literatur
1.
Zurück zum Zitat Schatz M, Rosenwasser L. The allergic asthma phenotype. J Allergy Clin Immunol Pract. 2014;2(6):645–8 quiz 649.CrossRef Schatz M, Rosenwasser L. The allergic asthma phenotype. J Allergy Clin Immunol Pract. 2014;2(6):645–8 quiz 649.CrossRef
2.
Zurück zum Zitat Ohtsu H, Seike M. Histamine and histamine receptors in allergic dermatitis. Handb Exp Pharmacol. 2017;241:333–45.CrossRef Ohtsu H, Seike M. Histamine and histamine receptors in allergic dermatitis. Handb Exp Pharmacol. 2017;241:333–45.CrossRef
3.
Zurück zum Zitat Roberts G, Xatzipsalti M, Borrego LM, Custovic A, Halken S, Hellings PW, Papadopoulos NG, Rotiroti G, Scadding G, Timmermans F, et al. Paediatric rhinitis: position paper of the European academy of allergy and clinical immunology. Allergy. 2013;68(9):1102–16.PubMed Roberts G, Xatzipsalti M, Borrego LM, Custovic A, Halken S, Hellings PW, Papadopoulos NG, Rotiroti G, Scadding G, Timmermans F, et al. Paediatric rhinitis: position paper of the European academy of allergy and clinical immunology. Allergy. 2013;68(9):1102–16.PubMed
4.
Zurück zum Zitat Rozalski M, Rudnicka L, Samochocki Z. Atopic and non-atopic eczema. Acta Dermatovenerol Croat. 2016;24(2):110–5.PubMed Rozalski M, Rudnicka L, Samochocki Z. Atopic and non-atopic eczema. Acta Dermatovenerol Croat. 2016;24(2):110–5.PubMed
5.
Zurück zum Zitat Group on Childhood Asthma. Third nationwide survey of childhood asthma in urban areas of China. Chin J Pediatr. 2013;2013(10):729–35. Group on Childhood Asthma. Third nationwide survey of childhood asthma in urban areas of China. Chin J Pediatr. 2013;2013(10):729–35.
6.
Zurück zum Zitat Guo Y, Li P, Tang J, Han X, Zong W, Wang H, Liu Q, Xiao F, Zou X, Wei F. Prevalence of skin diseases in pre-school children aged 0-7 years in 12 cities of China. Chin J Dermatol. 2017;11:790–4. Guo Y, Li P, Tang J, Han X, Zong W, Wang H, Liu Q, Xiao F, Zou X, Wei F. Prevalence of skin diseases in pre-school children aged 0-7 years in 12 cities of China. Chin J Dermatol. 2017;11:790–4.
7.
Zurück zum Zitat Zhang Y, Li B, Huang C, Yang X, Qian H, Deng Q, Zhao Z, Li A, Zhao J, Zhang X, et al. Ten cities cross-sectional questionnaire survey of children asthma and other allergies in China. Chin Sci Bull. 2013;58(34):4182–9.CrossRef Zhang Y, Li B, Huang C, Yang X, Qian H, Deng Q, Zhao Z, Li A, Zhao J, Zhang X, et al. Ten cities cross-sectional questionnaire survey of children asthma and other allergies in China. Chin Sci Bull. 2013;58(34):4182–9.CrossRef
8.
Zurück zum Zitat Kong WJ, Chen JJ, Zheng ZY, Shi QM, Zhou Y. Prevalence of allergic rhinitis in 3-6-year-old children in Wuhan of China. Clin Exp Allergy. 2009;39(6):869–74.CrossRef Kong WJ, Chen JJ, Zheng ZY, Shi QM, Zhou Y. Prevalence of allergic rhinitis in 3-6-year-old children in Wuhan of China. Clin Exp Allergy. 2009;39(6):869–74.CrossRef
9.
Zurück zum Zitat Barnish MS, Tagiyeva N, Devereux G, Aucott L, Turner S. Diverging prevalences and different risk factors for childhood asthma and eczema: a cross-sectional study. BMJ Open. 2015;5(6):e008446.CrossRef Barnish MS, Tagiyeva N, Devereux G, Aucott L, Turner S. Diverging prevalences and different risk factors for childhood asthma and eczema: a cross-sectional study. BMJ Open. 2015;5(6):e008446.CrossRef
10.
Zurück zum Zitat Strong C, Chang LY. Family socioeconomic status, household tobacco smoke, and asthma attack among children below 12 years of age: gender differences. J Child Health Care. 2014;18(4):388–98. Strong C, Chang LY. Family socioeconomic status, household tobacco smoke, and asthma attack among children below 12 years of age: gender differences. J Child Health Care. 2014;18(4):388–98.
11.
Zurück zum Zitat Miyake Y, Tanaka K. Lack of relationship between birth conditions and allergic disorders in Japanese children aged 3 years. J Asthma. 2013;50(6):555–9.CrossRef Miyake Y, Tanaka K. Lack of relationship between birth conditions and allergic disorders in Japanese children aged 3 years. J Asthma. 2013;50(6):555–9.CrossRef
12.
Zurück zum Zitat Kanoh M, Kaneita Y, Hara M, Harada S, Gon Y, Kanamaru H, Ohida T. Longitudinal study of parental smoking habits and development of asthma in early childhood. Prev Med. 2011;54(1):94–6.CrossRef Kanoh M, Kaneita Y, Hara M, Harada S, Gon Y, Kanamaru H, Ohida T. Longitudinal study of parental smoking habits and development of asthma in early childhood. Prev Med. 2011;54(1):94–6.CrossRef
13.
Zurück zum Zitat Zein JG, Erzurum SC. Asthma is Different in Women. Curr Allergy Asthma Rep. 2015;15(6):28.CrossRef Zein JG, Erzurum SC. Asthma is Different in Women. Curr Allergy Asthma Rep. 2015;15(6):28.CrossRef
14.
Zurück zum Zitat Fuseini H, Newcomb DC. Mechanisms Driving Gender Differences in Asthma. Curr Allergy Asthma Rep. 2017;17(3):19.CrossRef Fuseini H, Newcomb DC. Mechanisms Driving Gender Differences in Asthma. Curr Allergy Asthma Rep. 2017;17(3):19.CrossRef
15.
Zurück zum Zitat Simonsen AB, Deleuran M, Mortz CG, Johansen JD, Sommerlund M. Allergic contact dermatitis in Danish children referred for patch testing - a nationwide multicentre study. Contact Dermat. 2014;70(2):104–11.CrossRef Simonsen AB, Deleuran M, Mortz CG, Johansen JD, Sommerlund M. Allergic contact dermatitis in Danish children referred for patch testing - a nationwide multicentre study. Contact Dermat. 2014;70(2):104–11.CrossRef
16.
Zurück zum Zitat Haataja P, Korhonen P, Ojala R, Hirvonen M, Paassilta M, Gissler M, Luukkaala T, Tammela O. Asthma and atopic dermatitis in children born moderately and late preterm. Eur J Pediatr. 2016;175(6):799–808.CrossRef Haataja P, Korhonen P, Ojala R, Hirvonen M, Paassilta M, Gissler M, Luukkaala T, Tammela O. Asthma and atopic dermatitis in children born moderately and late preterm. Eur J Pediatr. 2016;175(6):799–808.CrossRef
17.
Zurück zum Zitat Tronnes H, Wilcox AJ, Lie RT, Markestad T, Moster D. The association of preterm birth with severe asthma and atopic dermatitis: a national cohort study. Pediatr Allergy Immunol. 2013;24(8):782–7.CrossRef Tronnes H, Wilcox AJ, Lie RT, Markestad T, Moster D. The association of preterm birth with severe asthma and atopic dermatitis: a national cohort study. Pediatr Allergy Immunol. 2013;24(8):782–7.CrossRef
18.
Zurück zum Zitat Matheson MC, DO AL, Burgess JA, Giles GG, Hopper JL, Johns DP, Abramson MJ, Walters EH, Dharmage SC. Preterm birth and low birth weight continue to increase the risk of asthma from age 7 to 43. J Asthma. 2017;54(6):616–23.CrossRef Matheson MC, DO AL, Burgess JA, Giles GG, Hopper JL, Johns DP, Abramson MJ, Walters EH, Dharmage SC. Preterm birth and low birth weight continue to increase the risk of asthma from age 7 to 43. J Asthma. 2017;54(6):616–23.CrossRef
19.
Zurück zum Zitat Xu XF, Li YJ, Sheng YJ, Liu JL, Tang LF, Chen ZM. Effect of low birth weight on childhood asthma: a meta-analysis. BMC Pediatr. 2014;14:275.CrossRef Xu XF, Li YJ, Sheng YJ, Liu JL, Tang LF, Chen ZM. Effect of low birth weight on childhood asthma: a meta-analysis. BMC Pediatr. 2014;14:275.CrossRef
20.
Zurück zum Zitat Kramer MS. Breastfeeding and allergy: the evidence. Annals Nutr Metab. 2011;59(Suppl 1):20–6.CrossRef Kramer MS. Breastfeeding and allergy: the evidence. Annals Nutr Metab. 2011;59(Suppl 1):20–6.CrossRef
21.
Zurück zum Zitat Lodge CJ, Tan DJ, Lau MX, Dai X, Tham R, Lowe AJ, Bowatte G, Allen KJ, Dharmage SC. Breastfeeding and asthma and allergies: a systematic review and meta-analysis. Acta Paediatr. 2015;104(467):38–53.CrossRef Lodge CJ, Tan DJ, Lau MX, Dai X, Tham R, Lowe AJ, Bowatte G, Allen KJ, Dharmage SC. Breastfeeding and asthma and allergies: a systematic review and meta-analysis. Acta Paediatr. 2015;104(467):38–53.CrossRef
22.
Zurück zum Zitat Dogaru CM, Nyffenegger D, Pescatore AM, Spycher BD, Kuehni CE. Breastfeeding and childhood asthma: systematic review and meta-analysis. Am J Epidemiol. 2014;179(10):1153–67.CrossRef Dogaru CM, Nyffenegger D, Pescatore AM, Spycher BD, Kuehni CE. Breastfeeding and childhood asthma: systematic review and meta-analysis. Am J Epidemiol. 2014;179(10):1153–67.CrossRef
23.
Zurück zum Zitat Cabana MD. The role of hydrolyzed formula in allergy prevention. Ann Nutr Metab. 2017;70(Suppl 2):38–45.CrossRef Cabana MD. The role of hydrolyzed formula in allergy prevention. Ann Nutr Metab. 2017;70(Suppl 2):38–45.CrossRef
24.
Zurück zum Zitat Almqvist C, Oberg AS. The association between caesarean section and asthma or allergic disease continues to challenge. Acta Paediatr. 2014;103(4):349–51.CrossRef Almqvist C, Oberg AS. The association between caesarean section and asthma or allergic disease continues to challenge. Acta Paediatr. 2014;103(4):349–51.CrossRef
25.
Zurück zum Zitat Schooling CM. Asthma and cesarean delivery. J Pediatr. 2016;176:221–4.CrossRef Schooling CM. Asthma and cesarean delivery. J Pediatr. 2016;176:221–4.CrossRef
26.
Zurück zum Zitat Brandao HV, Vieira GO, de Oliveira VT, Camargos PA, de Souza Teles CA, Guimaraes AC, Cruz AA, Cruz CMS. Increased risk of allergic rhinitis among children delivered by cesarean section: a cross-sectional study nested in a birth cohort. BMC Pediatr. 2016;16:57.CrossRef Brandao HV, Vieira GO, de Oliveira VT, Camargos PA, de Souza Teles CA, Guimaraes AC, Cruz AA, Cruz CMS. Increased risk of allergic rhinitis among children delivered by cesarean section: a cross-sectional study nested in a birth cohort. BMC Pediatr. 2016;16:57.CrossRef
27.
Zurück zum Zitat Almqvist C, Rejno G. Birth mode of delivery in the modern delivery ward - indication improves understanding of childhood asthma. Clin Exp Allergy. 2013;43(3):264–7.CrossRef Almqvist C, Rejno G. Birth mode of delivery in the modern delivery ward - indication improves understanding of childhood asthma. Clin Exp Allergy. 2013;43(3):264–7.CrossRef
28.
Zurück zum Zitat Goldacre A, Pakpoor J, Goldacre M. Perinatal characteristics and obstetric complications in mothers with multiple sclerosis: record-linkage study. Mult Scler Relat Disord. 2017;12:4–8.CrossRef Goldacre A, Pakpoor J, Goldacre M. Perinatal characteristics and obstetric complications in mothers with multiple sclerosis: record-linkage study. Mult Scler Relat Disord. 2017;12:4–8.CrossRef
29.
Zurück zum Zitat Shaheen SO, Macdonald-Wallis C, Lawlor DA, Henderson AJ. Hypertensive disorders of pregnancy, respiratory outcomes and atopy in childhood. Eur Respir J. 2016;47(1):156–65.CrossRef Shaheen SO, Macdonald-Wallis C, Lawlor DA, Henderson AJ. Hypertensive disorders of pregnancy, respiratory outcomes and atopy in childhood. Eur Respir J. 2016;47(1):156–65.CrossRef
30.
Zurück zum Zitat Nafstad P, Magnus P, Jaakkola JJ. Risk of childhood asthma and allergic rhinitis in relation to pregnancy complications. J Allergy Clin Immunol. 2000;106(5):867–73.CrossRef Nafstad P, Magnus P, Jaakkola JJ. Risk of childhood asthma and allergic rhinitis in relation to pregnancy complications. J Allergy Clin Immunol. 2000;106(5):867–73.CrossRef
31.
Zurück zum Zitat Liu X, Andersen SL, Olsen J, Agerbo E, Schlunssen V, Dharmage SC, Munk-Olsen T. Maternal hypothyroidism in the perinatal period and childhood asthma in the offspring. Allergy. 2018;73(4):932–9.CrossRef Liu X, Andersen SL, Olsen J, Agerbo E, Schlunssen V, Dharmage SC, Munk-Olsen T. Maternal hypothyroidism in the perinatal period and childhood asthma in the offspring. Allergy. 2018;73(4):932–9.CrossRef
32.
Zurück zum Zitat Gillman MW. Developmental origins of health and disease. N Engl J Med. 2005;353(17):1848–50.CrossRef Gillman MW. Developmental origins of health and disease. N Engl J Med. 2005;353(17):1848–50.CrossRef
33.
Zurück zum Zitat Barker DJ. The fetal and infant origins of adult disease. BMJ. 1990;301(6761):1111.CrossRef Barker DJ. The fetal and infant origins of adult disease. BMJ. 1990;301(6761):1111.CrossRef
34.
Zurück zum Zitat Rusconi F, Zugna D, Annesi-Maesano I, Baïz N, Barros H, Correia S, Duijts L, Forastiere F, Inskip H, Kelleher CC, et al. Mode of delivery and asthma at school age in 9 European birth cohorts. Am J Epidemiol. 2017;185(6):465–73.CrossRef Rusconi F, Zugna D, Annesi-Maesano I, Baïz N, Barros H, Correia S, Duijts L, Forastiere F, Inskip H, Kelleher CC, et al. Mode of delivery and asthma at school age in 9 European birth cohorts. Am J Epidemiol. 2017;185(6):465–73.CrossRef
35.
Zurück zum Zitat Freitas MS, de Córdoba LF, Monteiro JC, Solé D. Prevalence of rhinitis and associated factors in schoolchildren who live in the Amazon islands. Am J Rhinol Allergy. 2016;30(3):79–82.CrossRef Freitas MS, de Córdoba LF, Monteiro JC, Solé D. Prevalence of rhinitis and associated factors in schoolchildren who live in the Amazon islands. Am J Rhinol Allergy. 2016;30(3):79–82.CrossRef
36.
Zurück zum Zitat Wegienka G, Havstad S, Zoratti EM, Kim H, Ownby DR, Johnson CC. Combined effects of prenatal medication use and delivery type are associated with eczema at age 2 years. Clinical and experimental allergy. J Br Soc Allergy Clin Immunol. 2015;45(3):660–8.CrossRef Wegienka G, Havstad S, Zoratti EM, Kim H, Ownby DR, Johnson CC. Combined effects of prenatal medication use and delivery type are associated with eczema at age 2 years. Clinical and experimental allergy. J Br Soc Allergy Clin Immunol. 2015;45(3):660–8.CrossRef
37.
Zurück zum Zitat Ito J, Fujiwara T. Breastfeeding and risk of atopic dermatitis up to the age 42 months: a birth cohort study in Japan. Ann Epidemiol. 2014;24(4):267–72.CrossRef Ito J, Fujiwara T. Breastfeeding and risk of atopic dermatitis up to the age 42 months: a birth cohort study in Japan. Ann Epidemiol. 2014;24(4):267–72.CrossRef
38.
Zurück zum Zitat Stokholm J, Sevelsted A, Anderson UD, Bisgaard H. Preeclampsia associates with asthma, allergy, and eczema in childhood. Am J Respir Crit Care Med. 2017;195(5):614–21.CrossRef Stokholm J, Sevelsted A, Anderson UD, Bisgaard H. Preeclampsia associates with asthma, allergy, and eczema in childhood. Am J Respir Crit Care Med. 2017;195(5):614–21.CrossRef
39.
Zurück zum Zitat Harju M, Keski-Nisula L, Georgiadis L, Heinonen S. Parental smoking and cessation during pregnancy and the risk of childhood asthma. BMC Public Health. 2016;16:428.CrossRef Harju M, Keski-Nisula L, Georgiadis L, Heinonen S. Parental smoking and cessation during pregnancy and the risk of childhood asthma. BMC Public Health. 2016;16:428.CrossRef
40.
Zurück zum Zitat 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(9):1135–40.CrossRef 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(9):1135–40.CrossRef
41.
Zurück zum Zitat Leung JY, Li AM, Leung GM, Schooling CM. Mode of delivery and childhood hospitalizations for asthma and other wheezing disorders. Clin Exp Allergy. 2015;45(6):1109–17.CrossRef Leung JY, Li AM, Leung GM, Schooling CM. Mode of delivery and childhood hospitalizations for asthma and other wheezing disorders. Clin Exp Allergy. 2015;45(6):1109–17.CrossRef
Metadaten
Titel
Prenatal and neonatal factors involved in the development of childhood allergic diseases in Guangzhou primary and middle school students
verfasst von
Bolan Yu
Lijuan Dai
Juanjuan Chen
Wen Sun
Jingsi Chen
Lili Du
Nali Deng
Dunjin Chen
Publikationsdatum
01.12.2019
Verlag
BioMed Central
Erschienen in
BMC Pediatrics / Ausgabe 1/2019
Elektronische ISSN: 1471-2431
DOI
https://doi.org/10.1186/s12887-019-1865-0

Weitere Artikel der Ausgabe 1/2019

BMC Pediatrics 1/2019 Zur Ausgabe

Ähnliche Überlebensraten nach Reanimation während des Transports bzw. vor Ort

29.05.2024 Reanimation im Kindesalter Nachrichten

Laut einer Studie aus den USA und Kanada scheint es bei der Reanimation von Kindern außerhalb einer Klinik keinen Unterschied für das Überleben zu machen, ob die Wiederbelebungsmaßnahmen während des Transports in die Klinik stattfinden oder vor Ort ausgeführt werden. Jedoch gibt es dabei einige Einschränkungen und eine wichtige Ausnahme.

Alter der Mutter beeinflusst Risiko für kongenitale Anomalie

28.05.2024 Kinder- und Jugendgynäkologie Nachrichten

Welchen Einfluss das Alter ihrer Mutter auf das Risiko hat, dass Kinder mit nicht chromosomal bedingter Malformation zur Welt kommen, hat eine ungarische Studie untersucht. Sie zeigt: Nicht nur fortgeschrittenes Alter ist riskant.

Begünstigt Bettruhe der Mutter doch das fetale Wachstum?

Ob ungeborene Kinder, die kleiner als die meisten Gleichaltrigen sind, schneller wachsen, wenn die Mutter sich mehr ausruht, wird diskutiert. Die Ergebnisse einer US-Studie sprechen dafür.

Bei Amblyopie früher abkleben als bisher empfohlen?

22.05.2024 Fehlsichtigkeit Nachrichten

Bei Amblyopie ist das frühzeitige Abkleben des kontralateralen Auges in den meisten Fällen wohl effektiver als der Therapiestandard mit zunächst mehrmonatigem Brilletragen.

Update Pädiatrie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.