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Early life vitamin D status and asthma and wheeze: a systematic review and meta-analysis
BMC Pulmonary Medicinevolume 18, Article number: 120 (2018)
Vitamin D deficiency has been linked to an increased risk of asthma. This study aimed to quantify the effect of early life vitamin D status on asthma and wheeze later in life.
PubMed, Embase, CINAHL, and CNKI databases, the Cochrane Central Register of Controlled Trials, and Google Scholar were searched up to July 2017. We included randomized controlled trials (RCTs) and cohort studies with vitamin D level in blood (maternal or cord or infant) or intake (maternal intake during pregnancy or infant intake) and asthma and/or wheeze. Two reviewers independently extracted data. Fixed- and random-effects models were used to summarize the risk estimates of comparisons between highest vs. lowest vitamin D categories.
Of the 1485 studies identified, three RCTs and 33 cohort studies were included. We did not include the RCTs (1619 participants) in the meta-analysis as the comparators and outcome definitions were heterogenous. Three RCTs reported a non-statistically significant effect of vitamin D supplementation during pregnancy on offspring wheeze/asthma at 3 years of age. Pooled estimates of cohort studies suggest no association between antenatal blood vitamin D levels or vitamin D intake and offspring asthma assessed either > 5 years or ≤ 5 years. The estimate for blood vitamin D remained unchanged when two studies assessing asthma in adulthood were excluded, but a significant inverse association emerged between vitamin D intake and childhood asthma. We found no association between antenatal vitamin D level and wheeze. On the other hand, vitamin D intake during pregnancy may have a protective effect against wheeze.
The pooled estimates from cohort studies show no association between antenatal blood vitamin D level and asthma/wheeze in later life. Whereas, the pooled estimates from cohort studies suggest that antenatal vitamin D intake may have an effect on childhood asthma > 5 years or childhood wheeze. The inconsistent results from studies assessing vitamin D either in blood or intake may be explained by previously reported non-linear association between blood vitamin D3 and childhood asthma. Further trials with enough power and longer follow-up time should be conducted to confirm the results.
Asthma is an important cause of disability and a major worldwide public health concern. The prevalence of asthma in developed countries rose rapidly in the 1960s and has remained high since . More recently, the same rising trend has been observed in developing countries . While asthma affects people of all ages, the surge among children has been most marked .
Among the environmental factors that contribute to asthma, vitamin D status has generated increasing interest for the vitamin’s purported immunomodulatory properties.
Clinically, serum calcifediol [25(OH)D] is used as a marker of vitamin D level . In various populations calcifediol levels in cord blood are strongly correlated with maternal levels during pregnancy , with maternal calcifediol as the source of the fetal vitamin D pool . Vitamin D deficiency in pregnant women and infants is common worldwide, including both developed and developing countries, ranging from 45 to 90% in pregnant women and 61–94% in infants [5, 7,8,9]. Based on growing epidemiological evidence, vitamin D deficiency has been linked to an increased risk of respiratory infections and asthma . However, it is still unclear if and to what extent antenatal or early postnatal vitamin D deficiency would affect the development of wheeze or asthma later in life. Previous reviews on vitamin D supplementation during pregnancy have given conflicting messages [11,12,13].
Given that there have been further published studies (including trials), we undertook a systematic review aiming to address whether antenatal or early postnatal vitamin D status (including intake and blood level, both maternal and in infant) has any impact on the risk of developing asthma and wheeze later in life.
We followed the Meta-analysis of Observational Studies in Epidemiology (MOOSE)  and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines  when conducting and presenting this systematic review and meta-analysis. PRISMA and MOOSE checklist can be found in Additional file 1: Supplement 1. The review protocol was registered previously with the International Prospective Register of Systematic Reviews (PROSPERO Registration No. CRD42013005559) . The initial protocol considered asthma/wheeze, allergic rhinitis, atopic dermatitis (eczema), food allergy and atopic sensitization, but here we focus on asthma and wheeze.
Data sources and searches
We conducted a systematic literature search using PubMed, Embase, CINAHL, and CNKI (in Chinese) databases and Google Scholar for studies published up to 19th July 2017 and the Cochrane Central Register of Controlled Trials that reported data on antenatal or early postnatal vitamin D status or intervention and asthma and wheezing in children or adults. Details of the search strategy are provided in Additional file 1: Supplement 2.
The present systematic review focused on the effect of vitamin D level in blood (maternal or cord or infant) and intake (maternal intake during pregnancy or infant intake) on asthma and wheeze. We included randomized controlled trials (RCTs), quasi-randomized controlled trials, non-randomized controlled trials, prospective and retrospective cohort studies that measured maternal vitamin D status during any trimester of pregnancy or cord blood or offspring vitamin D status during infancy, and having asthma or wheeze during childhood or adulthood as outcomes, which (i) were diagnosed by doctors (including parental or self-reports), or (ii) required the use of asthma medication, or (iii) as assessed by the International Study of Asthma and Allergies in Children (ISAAC) questionnaire (Additional file 1: Supplement 3). Two reviewers (SS and WX) independently screened the titles and abstracts and identified potentially relevant publications according to the selection criteria, of which full text was obtained and read (online Additional file 1: Supplement 4). The reference lists of all papers of interest were scrutinized to obtain other relevant articles. Disagreements over inclusion were resolved through consensus, and where necessary, a third reviewer (JL) was involved.
Data extraction and risk of Bias assessment
The same reviewers independently extracted data using a standard data extraction form. We collected data on the number of subjects with and without asthma or wheeze in the antenatal or early postnatal vitamin D exposed/intervention and non-exposed/control groups; risk estimates (crude and/or adjusted odds ratios [ORs], relative risks [RRs] and hazard ratios [HRs]) and the corresponding 95% confidence intervals (CIs) at any available age end point. Furthermore, we recorded information on the population, geographical location, inclusion and exclusion criteria, interval of follow up, exposure measurement, outcome definition, measurement and window of assessment, and confounders (more details in Additional file 1: Supplement 5). Study authors were contacted when missing data was an issue. Disagreements on data extraction were checked against the original articles and/or resolved by a third reviewer. The data extracted were entered into Review Manager software and were double checked by two reviewers. Risk of bias was assessed using the tool recommended by the Cochrane Collaboration [17, 18]. Two reviewers independently rated the risk of bias for each study as high, low, or unclear (‘Definitely yes’ in the tool was considered as ‘low’ risk, ‘Definitely no’ as ‘high’ risk, ‘unclear’ comprised ‘probably yes’ and ‘probably no’ as specified in the tools ). Disagreements were resolved by discussion or by involving a third reviewer. Each cohort study was classified into one of the following categories: high (more than two criteria not applied/met); moderate (one or two criteria not applied/met or unclear); and low risk of bias (all criteria applied/met).
Data synthesis and analysis
We pooled the original risk estimates as reported (most being ORs) and used adjusted risk estimates where available. When only frequency distributions were provided, we calculated unadjusted ORs and their 95% CIs from the outcome distribution of exposed and non-exposed groups. Where outcome assessment was done in multiple time points in a study, we chose the one with the longest follow-up period or the time point when the age of the participants was comparable to other studies.
We pooled the risk estimates from each study that compared the risk in the highest vitamin D concentration or intake category with the lowest (which is the referent category), and also the risk in vitamin D sufficiency (≥75 nmol/L ) with deficiency (< 50 nmol/L according to the Institute of Medicine (IOM) definition ). As it could be difficult to diagnose asthma in children below 5 years of age, we stratified the studies on asthma according to the age of outcome assessment (> 5 years and ≤ 5 years). For exploring the association between blood vitamin D status and childhood asthma, a sensitivity analysis was performed by excluding the studies assessing the outcome in adulthood. We contacted the authors of the studies (n = 8) that had different cut-off values, and asked them to re-analyze their data according to the above categorization scheme. Of the eight authors contacted, four responded and provided additional data [20,21,22,23].
Both fixed-effects and random-effects models were used to summarize the effect sizes. Heterogeneity was evaluated by using the Q (P > 0.10 in the Chi2 test for low heterogeneity) and I2 statistics (moderate heterogeneity for I2 > 30% and considerable heterogeneity for ≥75%). We presented pooled ORs from random-effect models when considerable heterogeneity was observed. Stratified analyses by time window of vitamin D and outcome assessment (for wheeze only), latitude, geographical region, adjustment for family history of allergic disease, seasonality, and smoking status, methods of exposure and outcome ascertainment, and risk of bias were performed to explore the sources of heterogeneity. Funnel plots and Egger’s test were used to explore the possibility of publication bias. Number needed to treat for preventing asthma by increasing from low to high levels of vitamin D or via supplementation was estimated by the baseline asthma prevalence estimates and pooled ORs . Statistical analyses were performed with Review Manager software version 5.3  and STATA version 13.
We have identified 423 potentially relevant publications from PubMed, 855 from Embase, 36 from CNKI database, 105 from CINAHL and 66 from Google Scholar. After excluding duplicates and publication that did not meet the inclusion criteria, three RCTs [26,27,28] and 33 cohort studies [20,21,22,23, 29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57] were included (Fig. 1).
The main characteristics of the eligible RCTs, cohort studies and those studies excluded during full text screening are shown in Tables 1 and 2 and Additional file 1: Table S1, respectively. Two of the three RCTs were single-center trials and recruited low-risk pregnant women. The other was a multicenter trial enrolling pregnant women who had history of allergic disease. The dose of vitamin D administration and outcome definition varied across the three trials (1619 participants) (Table 1). The median ages of outcome assessment in cohort studies that reported association between blood vitamin D level and asthma, vitamin D intake and asthma, blood vitamin D and wheeze, and vitamin D intake and wheeze were 6 years (range 1.5–25), 5 (1.5–31), 5 (1–10), and 3 (1–10), respectively. Only two studies assessed the outcome in adulthood [36, 57]. Of the cohort studies, 26 studies reported data on asthma and 17 on wheeze. Nineteen of these 26 asthma studies measured vitamin D levels (31,940 participants from 13 cohorts were included in the meta-analysis); the rest assessed dietary/supplement intake (41,952 participants). A variety of operational definitions of asthma were used, including parental reports of doctor-diagnosed asthma (n = 7), parental reports of asthma medication use (n = 1), a combination of both (n = 2), parental reports of doctor-diagnosed asthma with wheezing symptom (n = 4), parental reports of doctor-diagnosed asthma and wheezing and/or asthma medication use (n = 5) and doctor-diagnosed asthma or asthma medication use by medical record review (n = 5). Two studies did not report the definition of asthma. All 17 studies on wheeze assessed maternal vitamin D status during pregnancy, with 12 measuring blood vitamin D levels (8123 participants from 8 cohorts were meta-analyzed) and 6 recorded intake (5678 participants). Most wheeze studies defined outcome using parental reports of wheezing symptoms in the past 12 months (Table 2).
Early life vitamin D status and asthma
Two RCTs [27, 28] reported non-significant trends of vitamin D supplementation during pregnancy on preventing the development of offspring asthma (OR, 0.82; 95% CI 0.50–1.36 and HR, 0.8; 95% CI, 0.6–1.0, respectively). As the intervention and the outcome definition were different, we did not pool the effect size. Apart from having insufficient information to assess allocation concealment, risk of bias was low in both RCTs (Additional file 1: Figure S1).
Figure 2 and Table 3 show the results from cohort studies as well as overall and subgroup summary ORs for the relationship between blood vitamin D and the risk of asthma assessed at > 5 years of age. Fix-effects ORs were not significant for the highest vs. the lowest categories of blood vitamin D concentrations (8 cohort studies, 28,436 participants, Fig. 2a) and for the sufficient vs. deficient groups (5 cohort studies, 23,339 participants, Fig. 2b), with moderate heterogeneity. The pooled estimate did not change materially (OR 0.91, 95% CI 0.73, 1.12, I2 = 32%, for highest vs. lowest; OR 1.02, 95% CI 0.84, 1.24, I2 = 47% for sufficient vs. deficient groups) after excluding one study assessing asthma in adulthood. Little heterogeneity was observed across subgroups, in studies measuring cord blood vitamin D level, adjusted for family history of allergic disease, or seasonality, those with exposure measured by liquid chromatography-tandem mass spectrometry (LC-MS/MS), and studies with moderate risk of bias (Table 3).
Figure 3 and Table 3 show the results from cohort studies and the overall and subgroup summary ORs for the relationship between blood vitamin D and the risk of asthma assessed at ≤5 years of age. The fixed-effects ORs were 0.81 (95% CI 0.65, 1.01, I2 = 0%, 6 cohort studies, 27,776 participants, Fig. 3a) for the highest vs. lowest categories of blood vitamin D concentrations and 0.93 for the sufficient vs. deficient groups (95% CI 0.85, 1.03, I2 = 36%, 6 cohort studies, 27,776 participants, Fig. 3b). Although higher maternal blood vitamin D level during pregnancy was significantly associated with lower risk of asthma assessed at ≤5 years, we did not observe any significant associations in the stratified analyses for studies that had more robust methodology (adjusting for further confounders, e.g. family history of atopy, seasonality, smoking status; blood calcifediol measured by the gold standard LC-MS/MS; studies with lower risk of bias) (Table 3). Six eligible cohort studies [38, 39, 43, 44, 46, 47] analyzed blood vitamin D as a continuous variable and we found no association with childhood asthma.
There was no association between vitamin D intake and asthma at ≤5 years (6 cohorts, 35,257 participants) or > 5 years (3 cohorts, 32,023 participants) (Table 4). A significant inverse association between vitamin D intake and asthma at ≤5 years of age emerged when we restricted our analysis to studies that did not adjust for seasonality or had high risk of bias, with low heterogeneity within these subgroups; and between vitamin D intake and asthma at > 5 years of age when we restricted to studies that adjusted for family history of atopy, seasonality or smoking status, or those that assessed outcome in childhood (OR 0.73, 95% CI 0.56, 0.94, I2 = 0%, 25,301 participants from 2 studies, for highest vs. lowest) (Table 4). The number needed to treat to prevent one case of asthma was 39 (range 25–93) via maternal vitamin D supplementation (Additional file 1: Table S2).
Studies that measured blood vitamin D concentrations generally had a low risk of bias except for attrition bias due to incomplete outcome data, confounding bias, and detection bias in the assessment of prognostic factors (Additional file 1: Figures S2 and S3). Several studies that assessed vitamin D intake had a high risk of detection bias due to recall of vitamin D intake, confounding bias, and attrition bias due to incomplete outcome data. (Additional file 1: Figures S4 and S5). No evidence of publication bias was found from the funnel plots or Egger’s tests for blood (P = 0.963 for asthma > 5 years and P = 0.655 for asthma ≤5 years) and intake (P = 0.913 for asthma > 5 years and P = 0.410 for asthma ≤5 years) (Additional file 1: Table S3).
Early life vitamin D status and wheeze
All three RCTs [26,27,28] used wheeze as primary outcome (one combined with asthma ). Two RCTs found no definitive effect of vitamin D supplementation during pregnancy on wheeze among offspring by 3 years of age (OR 0.86; 95% CI 0.49, 1.50; HR 0.76; 95% CI 0.52, 1.12) and one found a borderline statistical significance association (HR 0.8; 95% CI 0.6, 1.0). We did not perform pooled analysis for wheeze because of the major differences in intervention. Risks of performance and attrition bias were considered to be high due to missing outcome data and the lack of blinding in the trial conducted by Goldring et al.  (Additional file 1: Figure S1).
We did not observe significant association between maternal vitamin D concentrations during pregnancy and offspring wheeze in cohort studies (8123 participants from 8 studies, OR 0.91, 95% CI 0.76, 1.09 for highest vs. lowest levels, I2 = 25%; 2324 participants from 3 studies, OR 0.91, 95% CI 0.70, 1.19 for ≥75 nmol/L vs. < 50 nmol/L, I2 = 0%) (Fig. 4). Similar results were observed in stratified analyses (Table 5). Within-group inconsistency disappeared or was attenuated in studies that measured vitamin D intake during pregnancy or adjusted for family history of atopy or seasonality or blood calcifediol measured by LC-MS/MS or studies with moderate risk of bias. The overall fixed-effects OR of wheeze relating to maternal vitamin D intake was 0.66 (95% CI 0.53, 0.82; 5238 participants from 6 studies, I2 = 52%, Table 5). The association remained statistically significant when restricting to studies that: assessed outcome at or before 3 years of age and after 3 years of age, were conducted in a temperate area, adjusted for family history of atopy or seasonality, and those that had lower risk of bias. The Baiz paper  did not find an association in early transient, late onset or persistent wheeze, while Camargo et al.  reported a significant protective effect by 5 years of age (OR 0.95, 95% CI 0.91, 0.99), but this has not been consistent in earlier time windows reported in the studies by Camargo et al.  and Visness et al. 
The 12 cohort studies that investigated blood vitamin D levels and wheeze were evaluated to have low risk of bias, in terms of participant selection, exposure assessment, and window of outcome assessment and co-intervention. Some studies had high or unclear risk of confounding bias, detection bias and attrition bias (Additional file 1: Figure S6, a and b). Overall, the studies on vitamin D intake had higher risk of bias, due to their inadequacy in exposure assessment, assessment and adjustment for prognostic factors, and outcome follow-up (Additional file 1: Figure S7, a and b). There was no evidence of publication bias from the funnel plots or Egger’s tests for blood (P = 0.772) and intake (P = 0.954) (Additional file 1: Table S3).
This meta-analysis of cohort studies found no statistically significant association between vitamin D levels in maternal or cord blood or intake in early life and asthma either at > 5 or ≤ 5 years of age, with no evidence of publication bias. Of the cohort studies included, only two studies assessed asthma in adulthood [36, 57]. The exclusion of these two studies did not change the pooled estimate for blood vitamin D levels, while a significant inverse association between early life vitamin intake and childhood asthma at > 5 years emerged. We found no association between early life vitamin D level and risk of wheeze in later life. On the other hand, findings from cohort studies seemed to suggest a lower risk of wheeze associated with maternal vitamin D intake during pregnancy.
Variations in the intervention and outcome definition in three identified RCTs made it difficult to pool the effect size for wheeze or asthma associated with vitamin D supplementation during pregnancy. Two more recent trials [27, 28] with lower risk of bias also found non-statistically significant benefit for persistent/recurrent wheeze or asthma in the first 3 years of life. The results of RCTs were in line with the results of our meta-analysis of cohort studies, where we found non-significant trends of vitamin D supplementation for preventing offspring asthma at ≤5 years. However, our findings from cohort studies also suggest that early-life vitamin D intake may have an effect on childhood asthma at age > 5 years and childhood wheeze. Longer follow-up time for assessing the effect of vitamin D intake against asthma is required in future RCTs to confirm these results .
There are two opposing views regarding the relationship between vitamin D exposure and asthma. One school of thought, based on growing epidemiological evidence, hypothesized a link between vitamin D deficiency in early life and development of asthma and other allergic diseases , thought to have begun as sunlight exposure decreased with industrialization and urbanization. Others argued, however, that the current asthma and allergic disease pandemic might have been the consequence of widespread vitamin D supplementation in food, backed by some historical evidence . Coincidentally, both low and high levels of vitamin D were reported to be related to asthma, in a U-shaped manner . Another study by Rothers et al. also found that both low (< 50 nmol/L) and high (≥100 nmol/L) levels of cord blood calcifediol were associated with increased IgE, which was related to subsequent risk of wheeze/asthma . In the present meta-analysis, the inconsistent results from studies assessing vitamin D either in blood or intake for childhood asthma/wheeze risk may be explained by the previously reported non-linear association between blood vitamin D3 and childhood asthma, which tends to be non-statistically significant by comparing the highest with lowest vitamin D levels . However, the dichotomized exposure in the present study limited the exploration of non-linear association.
The sources of heterogeneity, as indicated by the results from stratified analyses were: window of exposure assessment, whether family history of atopy or seasonality have been adjusted for, definition of outcome, risk of bias, and the method of assessing blood calcifediol. As suggested by Autier et al. , vitamin D level could be a biomarker and proxy for overall health and wellbeing of mothers and infants. However, as most of the cohort studies included did not adjust for health status of the participants, we were unable to exclude such potential confounding. In most of the studies included, tobacco smoking was adjusted for in the analysis, but other important confounders including family history of atopic diseases, seasonal variations in blood vitamin D levels, sedentary lifestyle and obesity [62,63,64] were less commonly considered. Nevertheless, results from our sensitivity analysis on studies reporting blood vitamin D level, which included only studies that adjusted for family history and seasonal variations, showed no material difference in the summary estimates compared with our main findings. Three of the cohort studies [35, 42, 47] measured serum calcifediol in both prenatal and postnatal periods, but these studies analyzed the associations between vitamin D measured at different time points with outcome separately and failed to explore the effect of persistent vitamin D deficiency on asthma. While the half-life of serum calcifediol is only about two weeks , it is possible that such misclassification in vitamin D status measured at only one time point could have biased the findings towards the null. A recent study conducted by Hollams et al. used mixed-effects logistic regression and found no longitudinal association between calcifediol concentrations as a continuous variable and asthma from 3 to 10 years of age .
On the issue of case definition, ascertaining childhood asthma in epidemiological studies has been challenging given the lack of definitive diagnostic criteria [66, 67]. Most studies defined asthma by either maternal report of doctor-diagnosed asthma, asthma medications use, or a combination of doctor-diagnosed asthma and either asthma medication or wheezing symptoms within the past year. Although not without caveats, such as under-reporting both diagnosed and undiagnosed conditions  and variable agreement with clinical records , these definitions have been widely used in research . In two studies asthma definition was not specified, adding further variability to outcome assessment and increased heterogeneity in our pooled analyses.
In general, studies investigating blood vitamin D levels had relatively low risk of bias in most domains except for confounding, detection, and attrition biases, whereas studies that used food frequency questionnaire to quantify vitamin D intake were at risk of misclassification bias as pregnant women often had to recall their dietary history from a few months previous.. Apart from detection bias, most vitamin D intake studies were also at risk of attrition bias for their inadequate follow-up duration or unknown difference between missing and available outcome data, as well as confounding bias in some studies which did not include major confounders. In addition to variation over time, different methods of blood vitamin D level quantification employed in different studies might also introduce inter-study variability. In the stratified analysis, we compared the risk estimates derived from studies that used the gold standard LC-MS/MS with those using other methods and found no material difference between the pooled estimates. Studies that investigated antenatal vitamin D intake and asthma at > 5 years of age tended to be small and their inclusion in the meta-analysis may explain the weak evidence observed.
Compared to previous related systematic reviews [11,12,13, 70], we have identified more cohort studies and included two recently published RCTs in the analysis. Only six cohort studies [20, 22, 23, 30, 33, 39] measuring maternal serum calcifediol during pregnancy or from cord blood and asthma risk were identified by Cassim et al. , but we have included 13 more studies [31, 32, 34,35,36,37,38, 41, 43,44,45,46,47], plus an additional 13 cohort studies [21, 22, 29,30,31, 33, 37,38,39,40, 42, 44, 46] to explore the association between calcifediol level in maternal blood or cord blood and wheeze risk. As a consequence of our more comprehensive approach in including various exposure metrics (intake and blood level, both maternal and in infant) in the search strategy and a critical risk of bias assessment using the risk of bias tool recommended by the Cochrane Collaboration [17, 18], we were able to demonstrate the existence of heterogeneity between studies in the findings, which lead us to a more conservative conclusion. In addition, we further studied the association between antenatal or early postnatal vitamin D level and asthma and wheeze using commonly accepted clinical cut-off values. We found no difference of risk of asthma or wheeze between sufficient and deficient vitamin D level groups, implying the optimal threshold for bone health may not necessarily be applicable for the respiratory and immune systems.
One of the limitations of this work is that we were unable to retrieve sufficient information for calculating pooled estimates from six eligible studies that analyzed vitamin D level as a continuous variable. We were able to identify one study that has examined infant blood vitamin D levels and their relationship to wheeze but none for asthma. Studies investigating the association between infant vitamin D levels and risk of childhood asthma should be encouraged, with designs that minimize detection, confounding, and follow-up biases.
The pooled estimates from cohort studies show no association between antenatal blood vitamin D level and asthma/wheeze in later life. On the other hand, although the interventional studies found a non-statistically significant benefit for asthma/wheeze in first 3 years of life, the pooled estimates from cohort studies suggest that early life vitamin D intake may have an effect on childhood asthma > 5 years or childhood wheeze. Should that be the case, this may point to a cost-effective intervention for childhood asthma. Further trials with enough power and longer follow-up time should be conducted to confirm the results.
body mass index
enzyme-linked immunosorbent assay
food frequency questionnaire
high performance liquid chromatography
Institute of Medicine
The International Study of Asthma and Allergies in Children
liquid chromatography-tandem mass spectrometry
Meta-analysis of Observational Studies in Epidemiology
Preferred Reporting Items for Systematic Reviews and Meta-Analyses
randomized controlled trial
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The authors would like to thank Professor Susan L. Prescott (Centre for Child Health Research, University of Western Australia, Perth, Australia), Dr. Anderson P. Jones (Centre for Child Health Research, University of Western Australia, Perth, Australia), Professor Anne L. Wright (Arizona Respiratory Center, at the University of Arizona, Tucson, AZ), Dr. Debra A. Stern (Arizona Respiratory Center, at the University of Arizona, Tucson, AZ), Dr. Jane SA Lucas (Clinical and Experimental Sciences Academic Unit, University of Southampton Faculty of Medicine, Southampton, UK), Dr. Katharine C Pike (Clinical and Experimental Sciences Academic Unit, University of Southampton Faculty of Medicine, Southampton, UK), Dr. Catharine R Gale (MRC Epidemiology Resource Centre (University of Southampton), Southampton General Hospital, Southampton) for re-analyzing and sending the data requested from their manuscripts. We also thank Professor Carlos A. Camargo, Jr., Dr. Andrew Wills and Dr. Bo L. Chawes for clarifying our queries relating to their manuscripts and Mr. Ian Henderson for helping the language editing of the manuscript.
This work was supported by the Guangzhou Science and Technology Bureau, Guangzhou, China (2012 J5100038, 201807010086). The funders had no role in study design, data collection and analysis, decision to publish, interpretation of data and preparation of the manuscript.
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