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Incidence and risk factors for food hypersensitivity in UK infants: results from a birth cohort study

  • 1, 2Email authorView ORCID ID profile,
  • 3,
  • 1,
  • 4,
  • 3,
  • 5,
  • 6,
  • 5,
  • 3,
  • 7 and
  • 1, 8
Clinical and Translational Allergy20166:1

https://doi.org/10.1186/s13601-016-0089-8

©  Grimshaw et al. 2016

  • Received: 3 July 2015
  • Accepted: 7 December 2015
  • Published:

Abstract

Background

The prevalence of food hypersensitivity in the UK is still largely open to debate. Additionally its pathogenesis is also unclear although it is known that there are differing phenotypes. Determining its prevalence, along with identifying those factors associated with its development will help to assess its clinical importance within the national setting and also add to the debate on appropriate prevention strategies.

Methods

A population based birth cohort study conducted in Hampshire, UK as part of the EuroPrevall birth cohort study. 1140 infants were recruited with 823 being followed up until 2 years of age. Infants with suspected food reactions were assessed including specific IgE measurement and skin prick testing. Diagnosis of food hypersensitivity was by positive double-blind, placebo-controlled food challenge (DBPCFC) where symptoms up to 48 h after the end of the food challenge were considered indicative of a food hypersensitivity. Factors associated with food hypersensitivity and its two phenotypes of IgE-mediated and non-IgE-mediated disease were modelled in a multivariable logistic regression analysis.

Results

Cumulative incidence of food hypersensitivity by 2 years of age was 5.0 %. The cumulative incidence for individual food allergens were hens’ egg 2.7 % (1.6–3.8); cows’ milk 2.4 % (1.4–3.5); peanut 0.7 % (0.1–1.3); soy 0.4 % (0.0–0.8); wheat 0.2 % (0.0–0.5) and 0.1 % (0.0–0.32) for fish. The cumulative incidence of IgE-mediated food allergy was 2.6 % with 2.1 % reacting to hens’ egg. For non-IgE-mediated food allergy the cumulative incidence was 2.4 % (cows’ milk 1.7 %). Predictors for any food hypersensitivity were wheeze, maternal atopy, increasing gestational age, age at first solid food introduction and mean healthy dietary pattern score. Predictors for IgE mediated allergy were eczema, rhinitis and healthy dietary pattern score whereas for non-IgE-mediated food allergy the predictors were dog in the home, healthy dietary pattern score, maternal consumption of probiotics during breastfeeding and age at first solid food introduction.

Conclusions

Just under half the infants with confirmed food hypersensitivity had no demonstrable IgE. In an exploratory analysis, risk factors for this phenotype of food hypersensitivity differed from those for IgE-mediated food allergy except for a healthy infant diet which was associated with less risk for both phenotypes.

Keywords

  • Food hypersensitivity
  • Food allergy
  • Epidemiology
  • EuroPrevall
  • Incidence
  • Risk factors
  • Dietary pattern analysis
  • Healthy eating

Background

Food hypersensitivity continues to be a concern for health care professionals and the general population since it adversely affects quality of life [1, 2] and household and healthcare expenditure [3, 4]. Any public health concern needs local incidence and prevalence data [5] and this is particularly relevant for food hypersensitivity due to conflicting opinions as to prevalence [6, 7]. There is also great interest in its potential risk factors due to its association with the development of other conditions [8, 9]. Since geographical issues are also important in the development of food hypersensitivity, not all previously identified risk factors may be associated with food hypersensitivity development in a UK cohort in infants. One study has looked at risk factors of food hypersensitivity development in the UK but it only considered dietary factors [10]. We have previously described the relationship between breast feeding, complementary feeding and dietary patterns and food hypersensitivity in this cohort. In this publication we now present data on the incidence of food allergy in the UK within a general UK cohort and describes the results of a follow up of 1140 infants pairs. In an additional exploratory analysis, we also aimed to investigate the possible risk factors for IgE and non-IgE mediated food allergy.

Methods

Study design

The PIFA (prevalence of infant food allergy) study is the UK cohort of the EuroPrevall project [11] which recruited 1140 babies between 2006 and 2008. Its design has been described elsewhere [11, 12] but the main points of its methodology are reported here. It received approval from Research and Development departments at the Royal Hampshire County Hospital, Winchester and Southampton General Hospital and ethical approval was granted by North and Mid Hampshire Local Research Ethics Committee and Southampton and South West Hampshire Local Research Ethics Committee (05/Q1703/34).

All eligible pregnant women registered with the Hampshire Hospitals Foundation Trust midwifery service were invited to take part in the study. Interested women met one of the study research fellows when informed consent was taken and baseline information on socio-economic, environmental and family allergy history was collected [12]. Potential reactions to food were identified via parental reporting and the 12 and 24 month questionnaires. Those infants displaying signs or symptoms which fulfilling the EuroPrevall-wide criteria for assessment as described in Keil et al. [12] and also detailed in Fig. 1 were invited to attend the Southampton Wellcome Trust Clinical Research Facility (WTCRF). Those who went on to meet the eligibility criteria to perform a double-blind, placebo-controlled challenge (DBPCFC) of an (Fig. 1) returned on two subsequent days for this to be carried out. Additional dietary intake data was invited from all study participants in the form of a prospective food diary kept for the first year of life [13, 14]. The study received ethics approval as detailed previously [13, 14].
Fig. 1
Fig. 1

Criteria for a defining ‘symptomatic children’ after telephone screening; b eligibility for double-blind placebo-controlled food challenge tests (used with Permission from Keil et al. [12])

Food hypersensitivity definitions

‘Parent perceived food hypersensitivity’ describes when a parent suspected their child had a reaction to food. A positive double-blind, placebo-controlled challenge (DBPCFC) was defined as either (1) objective immediate type symptoms or signs within 2 h of the final dose and/or (2) parentally reported objective signs of delayed reactions (vomiting, diarrhoea, hives and worsening of eczema), up to 48 h after challenge. With a positive DBPCFC, if there was a positive specific IgE (SpIgE) (≥0.35 kUl/L) or skin prick test (SPT) (wheal diameter ≥3 mm), the infant was described as food allergic [15]. Food hypersensitivity without sensitisation was described as ‘non-IgE food hypersensitivity’. ‘Food hypersensitivity’ is used to describe all positive DBPCFC.

Control infants

Every child with DBPCFC diagnosed food hypersensitivity was allocated two age-matched controls, who were selected by approaching parents of infants with birthdays just before or after the child with a confirmed food hypersensitivity until two controls were found. Since the control child was not selected until after a positive food challenge, some months may have passed between the time of the initial assessment of the case and the initial assessment of the control. There was however, never more than 4 weeks between the positive food challenge result and the assessment of the control child. Each control child was assessed in the same manner (apart from SPT) as the symptomatic infants, including a blood sample, to ensure they exhibited no signs of food allergy [12].

Statistical analysis

Analysis was carried out using SPSS version 21 (IBM, New York, USA) and STATA version 12 (College Station, USA). The infant healthy eating pattern score was derived by PCA analysis of the food diet data as described previously and describes the dietary component which accounted for 50 % of the variance and had high positive values associated with fruit, vegetable, fish and poultry consumption. Low/negative values associated with highly processed adult foods (such as ready meals, cook in-sauces, potato products and bacon) and the use of commercial baby foods more than once a day [13]. Cumulative incidence of food hypersensitivity was calculated with 95 % confidence intervals. Exploratory analyses assessed whether any potentially important exposures were significantly related to food hypersensitivity. A univariate logistic regression approach was taken followed by backwards multivariable analysis (which initially included factors with p < 0.1). Where the cells formed by the outcome and categorical predictor variables had no observations, exact logistic regression or the Bayesian firth logic approach was used to calculate odds ratios [16]. As an example of power for this exploratory analysis, with exposure rates of 62 and 35 % in cases and controls respectively and 41 cases and 82 controls, we had 80 % power to detect a significant relationship between the exposure and outcome at a 5 % level of significance (STATA version 12).

Results

Participants

1605 pregnant women initially expressed an interest in participating in the study. 402 mothers subsequently declined, mainly due to time commitments or unwillingness for their child to have blood tests. We had no ethical approval to collect further data about these women. 1203 infants were born of which 63 were excluded either because they did not satisfy the inclusion criteria (due to low apgar, premature delivery or delivery outside the recruitment period) or they had missing birth data. The resultant baseline cohort was 1140 (Table 1). A total of 823 (72.2 %) infants were followed up to 2 years (Fig. 2).
Table 1

Demographic, socioeconomic and familial factors of the study participants

 

All participants

Lost to follow up (2 years)

Eligible for DBPCFC

Not challenged

Challenged

Confirmed food hypersensitivity

n

1140

317

15

55

41

Baseline characteristics

 Caucasian ethnicity

1093 (95.8 %)

304 (96.0 %)

11 (73.3 %)

50 (90.9 %)

39 (95.1 %)

 Smoking during pregnancy

70 (6.1 %)

45 (14.2 %)

0 (0.0 %)

1 (1.8 %)

1 (2.4 %)

 Mothers’ mean age, years

31.9 (5.2)

30.0 (5.8)

31.9 (5.2)

32.0 (5.5)

31.6 (5.3)

 Fathers’ mean age, years

34.1 (5.7)

32.6 (6.4)

33.9 (5.1)

33.9 (4.5)

33.2 (4.6)

 Highest education of parents

  Low (up to 12y)

220 (19.3 %)

86 (27.2 %)

4 (26.7 %)

9 (16.4 %)

7 (17.1 %)

  Intermediate (>12 years, e.g. college)

331 (29.0 %)

96 (30.2 %)

3 (20.0 %)

19 (34.5 %)

13 (31.7 %)

  High (e.g. university)

565 (49.6 %)

121 (38.3 %)

8 (53.3 %)

27 (49.1 %)

21 (51.2 %)

 Allergies in family

  Maternal atopy (A, AR or E)

765 (67.1 %)

210 (66.4 %)

13 (86.7 %)

48 (87.3 %)

36 (87.8 %)

  Paternal atopy (A, AR or E)

610 (53.5 %)

170 (53.7 %)

11 (73.3 %)

30 (54.5 %)

23 (56.1 %)

  Maternal food hypersensitivity

249 (21.8 %)

77 (24.4 %)

6 (40.0 %)

13 (23.6 %)

11 (26.8 %)

  Paternal food hypersensitivity

135 (11.8 %)

35 (11.1 %)

1 (6.7 %)

7 (12.7 %)

6 (14.6 %)

 Urban living environment

273 (23.9 %)

99 (31.2 %)

6 (40.0 %)

11 (20.0 %)

8 (19.5 %)

 Mean number of sibs at home

1.7 (0.88)

1.8 (0.99)

1.4 (0.65)

1.6 (0.71)

1.5 (0.64)

 Female sex

557 (48.9 %)

166 (52.4 %)

6 (40.0 %)

23 (41.8 %)

17 (41.5 %)

 Animals in household at birth

  Any

566 (49.6 %)

164 (50.6 %)

8 (53.3 %)

33 (60.0 %)

26 (63.4 %)

  Cat

325 (28.5 %)

92 (28.4 %)

4 (26.6 %)

15 (27.3 %)

10 (24.4 %)

  Dog

204 (17.9 %)

66 (20.4 %)

3 (20.0 %)

15 (27.3 %)

13 (31.7 %)

 Season of birth (n = 1139)

  Summer

379 (33.3)

112 (34.6 %)

2 (13.3 %)

21 (38.2 %)

17 (41.5 %)

  Autumn

251 (22.0)

66 (20.4 %)

7 (46.6 %)

13 (23.6 %)

8 (19.5 %)

  Winter

183 (16.1)

51 (15.7)

2 (13.3 %)

9 (16.4 %)

8 (19.5 %)

  Spring

326 (28.6)

95 (29.3 %)

4 (26.6 %)

11 (20.0 %)

8 (19.5 %)

Figures represent numbers (%) or mean (SD)

A asthma, AR allergic rhinitis, E eczema

Fig. 2
Fig. 2

Flow of participants through the study

Cumulative incidence of food hypersensitivity

210 infants (25.5 %; 95 % CI 22.5–28.5) had parental perceived food hypersensitivity. 173 of these were identified via parental phone call to the study office and 61 were identified via administration of the questionnaire (55 at 12 months and 10 at 24 months). Of these 210 infants, 135 met the criteria for assessment and were invited for clinical assessment. Those not invited for assessment had other presentations, e.g. lactose intolerance and perioral rash with acidic foods. Of the 135 infants who underwent clinical assessment, 70 were eligible for a DBPCFC. Fifty-five infants underwent the DBPCFC and 41 of these had a positive DBPCFC giving a cumulative incidence of food hypersensitivity of 5.0 % (95 % CI 3.5–6.5). The cumulative incidence for individual foods were hens’ egg 2.7 % (1.6–3.8); cows’ milk 2.4 % (1.4–3.5); peanut 0.7 % (0.1–1.3); soy 0.4 % (0.0–0.8); wheat 0.2 % (0.0–0.5) and 0.1 % (0.0–0.32) for fish, lentil and broccoli (Fig. 1). Twelve infants were reactive to more than one food. The commonest parentally reported symptoms at assessment were physician diagnosed eczema (12 infants) and vomiting (11 infants).

Characteristics of participants with food hypersensitivity

Of the 41 infants with DBPCFC confirmed food hypersensitivity, 38 had SpIgE assessed and 40 were skin prick tested. Eczema was the presenting symptoms in 16 (39.0 %) of children with food hypersensitivity; gastrointestinal symptoms were the next most frequent (26.8 %). No child presented with a history of anaphylaxis (Table 2).
Table 2

Characteristics of participants with food hypersensitivity and their controls at initial assessment

 

Participants with food hypersensitivity (n = 41)

Control participants (n = 82)

p value

Median (IQR) age of child, months

9.3 (5.7–17.0)

14.9 (10.1–20.2)

0.024

Diagnostic criteria: positive DBPCFC

41 (100 %)

  

 History of anaphylaxis

0 (0 %)

  

Presenting symptoms

 Gastrointestinal

11 (26.8 %)

  

 Cutaneous (eczema and/or urticaria)

22 (46.3 %)

  

 Respiratory

4 (9.7 %)

  

 Other

3 (7.3 %)

  

 None

1 (2.4 %)

  

How soon did symptoms appear, minutes (SE) [Range]

170 (118) [0–4320]

  

Positive specific IgE (≥0.35 kU/l)

21 (51.2 %)

  

Median specific IgE, kU/l

1.85 (0.85–3.81)

  

Positive SPT (≥3 mm)

17 (41.4 %)

  

Median SPT weal diameter, mm

5.00 (3.00–6.25)

  

Eczema

32 (78.1 %)

45 (54.9 %)

0.005

Wheeze

17 (41.5 %)

21 (25.6 %)

0.054

Rhinitis

14 (34.1 %)

11 (13.4 %)

0.007

Assessment refers to the assessment of cases at presentation with food hypersensitivity and the equivalent assessment of their controls. Figures represent numbers (%) or mean (SD) or median (IQR)

Specific IgE and SPT data refer to the specific food that is being assessed in individual participants, where there is more than one food, the highest result is taken as representative. One case had no presenting symptoms as they were found to have a positive specific IgE to peanut on assessment as a control participant. P values represent a comparison between case of food hypersensitivity and controls; Chi squared test for categorical data, Mann–Whitney U test for non-parametric data or a two-sample t test for parametric data

DBPCFC double-blind, placebo-controlled food challenge

Potential risk factors for food hypersensitivity

Paternal, perinatal, environmental and infant nutritional factors were compared between cases of food hypersensitivity and controls (Tables 2, 3, 4; Additional file 1: Table S1). Data relating infant diet to food hypersensitivity has been published in detail elsewhere [14, 15].
Table 3

Maternal, parental, perinatal, environmental health and medicinal factors

 

Participants with food hypersensitivity (n = 41)

Control participants (n = 82)

p value

Maternal atopy

36 (87.8 %)

52 (63.4 %)

0.002

Paternal atopy

23 (57.5 %)

50 (61.0 %)

0.844

Mean maternal pre-pregnancy weight, kg

65.9 (14.0)

64.0 (11.5)

0.558

Mean maternal pre-pregnancy height, cm

164.1 (5.9)

165.0 (6.6)

0.690

Median parity

0.0 (0.0–1.0)

0.0 (0.0–1.0)

0.729

Singleton pregnancy

40 (97.6 %)

82 (100.0 %)

0.333

Maternal smoking in pregnancy

1 (2.4 %)

3 (3.7 %)

1.000

Other household smoking in pregnancy

8 (19.5 %)

5 (6.1 %)

0.027

Aspirin/paracetamol during pregnancy

30 (81.1 %)

49 (69.0 %)

0.132

Any anti-inflammatory during pregnancy

4 (11.1 %)

7 (9.9 %)

0.542

Maternal antibiotics during pregnancy

9 (22.0 %)

19 (23.3 %)

0.286

Mode of delivery

 Normal

20 (51.3 %)

37 (45.7 %)

0.860

 Caesarean

13 (31.7 %)

20 (24.4 %)

 Forceps

3 (7.3 %)

12 (14.8 %)

Mean gestation, weeks

39.5 (1.7)

40.0 (1.4)

0.062

Mean birth weight, grams

3480 (470)

3370 (562)

0.913

Antibiotics in first week of age

0 (0.0 %)

0 (0.0 %)

1.000

Environmental

 Urban living Environment

8 (19.5 %)

11 (13.4 %)

0.601

 Live on a main road

3 (7.3 %)

5 (6.1 %)

0.535

 Cat at home

10 (24.4 %)

24 (29.3 %)

0.365

 Dog at home

13 (31.7 %)

12 (14.6 %)

0.026

 Mould in home

5 (12.2 %)

8 (9.8 %)

0.457

 Type of flooring where baby sleeps

  Carpet

37 (90.2 %)

72 (87.8 %)

0.757

  Wooden, laminate or parquet

4 (9.8 %)

9 (11.0 %)

  Linoleum or vinyl tiles

0 (0.0 %)

1 (1.2 %)

Type of mattress your baby sleeps on

  Foam

29 (70.7 %)

51 (62.2 %)

0.362

  Synthetic

10 (24.4 %)

22 (26.8 %)

  Other

2 (4.9 %)

9 (11.0 %)

 Cleaning kitchen work surfaces

  Non-bactericidal

12 (29.3 %)

27 (32.9 %)

0.396

  Bactericidal

27 (65.9 %)

50 (61.0 %)

  Neither

1 (2.4 %)

5 (6.1 %)

  Do not know

1 (2.4 %)

0 (0.0 %)

 Cleaning table where you eat

  Spray cleaner

26 (63.4 %)

38 (46.3 %)

0.131

  Soap and Water

10 (24.4 %)

19 (23.2 %)

  Just water

2 (4.9 %)

6 (7.3 %)

  None of these

3 (7.3 %)

19 (23.2 %)

 Pacifier/dummy

  Latex

5 (12.2 %)

8 (9.8 %)

0.202

  Silicon

21 (51.2 %)

32 (39.0 %)

 Attendance at day care or a nursery

13 (31.7 %)

19 (23.2 %)

0.246

 Mean age when started day care or a nursery, months

7.3 (2.19)

8.74 (3.74)

0.269

Health

 Upper respiratory infection

  None

9 (23.7 %)

21 (27.6 %)

0.856

  Occasionally

20 (52.6 %)

36 (47.4 %)

  Often

9 (23.7 %)

19 (25.0 %)

 Lower respiratory infection

  None

34 (89.5 %)

71 (93.4 %)

0.462

  Occasionally

4 (10.5 %)

4 (5.3 %)

  Often

0 (0.0 %)

1 (1.3 %)

 Wheeze with upper respiratory infection

  None

24 (63.2 %)

59 (77.6 %)

0.195

  Occasionally

11 (28.9 %)

15 (19.7 %)

  Often

3 (7.9 %)

2 (2.6 %)

 Bronchiolitis (bronchitis)

  None

36 (94.7 %)

75 (98.7 %)

0.106

  Occasionally

2 (5.3 %)

1 (1.3 %)

  Often

0 (0.0 %)

0 (0.0 %)

 Middle ear infection

  None

32 (84.2 %)

70 (92.1 %)

0.165

  Occasionally

6 (15.8 %)

6 (7.9 %)

  Often

0 (0.0 %)

0 (0 %)

 Gastrointestinal illness

  None

30 (78.9 %)

69 (90.8 %)

0.125

  Occasionally

7 (18.4 %)

7 (9.2 %)

  Often

1 (2.6 %)

0 (0.0 %)

Medication

 Median number of antibiotics in last 12 months

1 (0–2)

0.5 (0–1)

0.341

 Mean age when first received antibiotics, months

8.65 (7.04)

8.44 (6.59)

0.964

 Received aspirin

1 (2.6 %)

0 (0.0 %)

0.333

 Received paracetamol

38 (100.0 %)

74 (97.4 %)

0.442

 Received anti-inflammatories (e.g. Ibuprofen, Nurofen)

29 (76.3 %)

51 (67.1 %)

0.214

 Received anti-reflux medication

11 (28.9 %)

10 (13.2 %)

0.039

 Received any vaccinations

37 (97.4 %)

73 (96.0 %)

0.565

 Received any skin creams, lotions or powders

33 (86.8 %)

55 (72.4 %)

0.079

Figures are numbers (%) in each group, means (SD) or medians (25th, 75th centiles) unless specified. P values relate to a comparison between cases and control; they represent a Chi squared test for categorical data, Mann–Whitney U test for non-parametric data and two sample t test for parametric data. All data was not available for all participants. Maternal atopy defined as any of maternal asthma, eczema, rhinitis or food allergy

Table 4

Univariate and multivariable analyses for infants with food hypersensitivity, IgE-mediated food allergy and non-IgE-mediated hypersensitivity

 

All infants will food hypersensitivity (n = 41) compared to control infants

Univariate

Multivariable*

Odds ratio (95 % CI)

p value

Odds ratio (95 % CI)

p value

Wheeze, (at initial assessment)

2.120 (0.940–4.782)

0.092

20.591 (1.465–289.341)

0.025

Maternal atopy

5.192 (1.683–16.017)

0.002

87.479 (1.021–7498.366)

0.049

Gestation, weeks

0.756 (0.585–0.978)

0.033

0.171 (0.045–0.642)

0.009

Age at first solids, weeks

0.920 (0.830–0.998)

0.044

0.506 (0.282–0.908)

0.022

Mean infant healthy eating dietary pattern score, arbitrary units

0.365 (0.229–0.583)

0.002

0.155 (0.028–0.868)

0.034

 

IgE-mediated (n = 21) compared to control infants

Non-IgE-mediated (n = 20) compared to control infants

Univariate

Multivariable**

Univariate

Multivariable**

Odds ratio

p

Odds ratio

p

Odds ratio

p

Odds ratio

p

Eczema (at initial assessment)

17.83* (2.89–∞)

<0.001

18.67**** (1.03–338.41)

0.048

    

Rhinitis (at initial assessment)

3.94 (1.31–11.83)

0.023

4.80**** (1.19–19.36)

0.027

2.96 (0.92–9.52)

0.087

  

Maternal atopy

11.54 (1.47–90.35)

0.003

      

Vitamin D supplement during pregnancy

8.68*** (0.66–∞)

0.097

      

Age at first egg from any source, months

1.05 (1.00–1.11)

0.026

Not included in analysis as likely reverse causality

    

Dog in the home

3.24 (1.00–10.48)

0.076

  

4.37 (1.38–13.80)

0.015

19.49 (1.17–325.93)

0.039

Wheeze associated with upper respiratory tract

2.84 (1.01–7.98)

0.052

      

Healthy eating dietary pattern score, arbitrary units

0.36 (0.20–0.66)

0.001

0.32**** (0.16–0.66)

0.012

0.34 (0.19–0.62)

<0.001

0.28 (0.09–0.87)

0.028

Maternal age, years

    

0.87 (0.78–0.99)

0.037

  

Paternal age, years

    

0.893 (0.803–0.992)

0.035

  

Maternal food hypersensitivity

    

2.790 (0.994–7.831)

0.055

  

Other household smoking

    

5.133 (1.32–19.95)

0.023

  

Consumed probiotics whilst breastfeeding

    

3.31 (1.13–9.75)

0.084

45.41 (3.41–604.67)

0.004

Age at first solid, months

    

0.84 (0.73–0.97)

0.021

0.60 (0.40–0.89)

0.011

Milk overlap, months

    

0.94 (0.88–1.00)

0.037

  

Received anti-reflux medication

    

3.312 (1.13–9.75)

0.030

Not included in analysis as likely reverse causality

Adjusted and unadjusted odds ratios (95 % confidence intervals (CI) and p values) are presented for all factors significant in the multivariate model

* Factors associated with hypersensitivity at a p value <0.1 were entered into a multivariable analysis using SPSS. A stepwise backwards selection process was used

** For multivariable analysis p values are only given for those variables included in the final model

*** Exact logistic regression model used to estimate parameters

**** Firthlogit approach to fit a logistic model by penalized maximum likelihood regression (accessed via STATA)

Factors significantly associated with food hypersensitivity were eczema, rhinitis, maternal atopy, anti-reflux medication, other household smoking, dog in the home and a variety of dietary factors including age at first solids, infant healthy eating dietary pattern score and reduced intake of milk whilst breastfeeding. (Tables 2, 3; Additional file 1: Table S1). The ‘infant received anti-reflux medication’ and ‘reduced maternal milk intake whilst breastfeeding’ variables were removed from further analyses since any association was likely to be due to reverse causality. The variable ‘other household smoking’ was also removed from further analyses since the significant association seen may be due to the low level seen in the control infants compared to all study participants and not a causal relationship. All the factors related to food hypersensitivity (p < 0.1) were included in the multivariable analysis (see Tables 2, 3; Additional file 1: Table S1–S9). After the multivariable analysis wheeze, maternal atopy, gestational age, age at first solids and mean healthy eating dietary pattern score remained independent factors in the model. Wheeze (aOR 20.59) and maternal atopy (aOR 87.48) were factors that increased risk of food hypersensitivity. Increasing gestational age (aOR 0.171), age at solid introduction (aOR 0.506) and healthy eating dietary pattern score (aOR 0.155) were associated with a significant reduction in risk (Table 4).

IgE-mediated food allergy compared to non-IgE-mediated food hypersensitivity

21 infants (cumulative incidence 2.6 %, 1.52–3.6) had IgE-mediated food allergy. Incidences for individuals foods were hens’ egg 2.1 % (1.1–3.0); cows’ milk 0.7 % (0.2–1.3); peanut 0.6 % (0.1–1.1); and 0.1 % (0.0–0.4) for soy, wheat and fish. Eight infants reacted to more than one food. Infants with non-IgE-mediated food hypersensitivity reacted most frequently to cows’ milk (1.7 %, 0.8–2.6) then hens’ egg (0.6 %, 0.1–1.1; soy (0.2 %, 0.0–0.6); and peanut, wheat, lentil and broccoli (0.1 %, 0.0–0.4). Four infants reacted to more than one food. No infant had both IgE-mediated allergy and non-IgE-mediated food reactions (Additional file 1: Table S2) and no infant with IgE ≥0.35 kU/l had symptoms after 2 h of ingesting the culprit food (Additional file 1: Table S3).

There were significant differences between the two phenotypes of food hypersensitivity. When comparing the two phenotypes, significant differences were found for maternal food hypersensitivity (0.013), mean time to reaction after food ingestion (p = 0.007), current eczema (p = 0.028), an urban living environment (p = 0.015), fish oil supplement use during pregnancy (p = 0.025), probiotic use during breastfeeding (p = 0.009) and day care attendance (p = 0.025) (Additional file 1: Table S3).

Risk factors for IgE- and non-IgE-mediated reactions differed (Additional file 1: Tables S4–S9). For infants with IgE-mediated food allergy (n = 21), they were current eczema, current rhinitis, maternal atopy, wheeze with an upper respiratory tract infection, vitamin D supplementation during pregnancy and infant healthy infant diet score. In a multivariable analysis, the independent risk factors for IgE-mediated food allergy were eczema (aOR 18.67, 1.03–338.41), rhinitis (aOR 4.80, 1.19–19.36) and infant healthy eating dietary pattern score (aOR 0.32, 0.16–0.66). In contrast, for infants with non-IgE-mediated food hypersensitivity (n = 20), the risk factors were a dog in the home, infant healthy eating dietary pattern score, maternal age, paternal age, other household smoking, anti-reflux medication use, age at first solids and concurrent breastfeeding with cows’ milk from any source. In a multivariable analysis, the independent risk factors for non-IgE-mediated food hypersensitivity were dog in the home (aOR 19.49, 1.17–325.93), consuming probiotics whilst breastfeeding (aOR 45.41, 3.41–604.67), age at first solid food introduction (aOR 0.60, 0.40–0.89) and infant healthy eating dietary pattern score (aOR 0.28, 0.09–0.87) (Table 4).

Discussion

In this UK cohort we found the cumulative incidence of DBPCFC confirmed food hypersensitivity to be 5.0 % (3.7–6.7). This is a little higher than other published figures of 0.0–4.2 % in the 0–5 year age group [5]. This is probably due to methodological differences since many studies only performed DBPCFC if there was sensitisation thus potentially missing non-IgE-mediated food hypersensitivity. The observed difference may also be due to geographical differences since it is thought the incidence of food hypersensitivity reactions is higher in Northern European countries [5].

Since all children with a clinical history of food hypersensitivity were challenged in this study, a cumulative incidence for both IgE- and non-IgE-mediated conditions could be determined: 2.6 % (1.5–3.6) for IgE-mediated food allergy and 2.4 % (1.4–3.5) for non-IgE-mediated food hypersensitivity. There is a lack of published data for non-IgE-mediated food hypersensitivity for comparison, but our results are broadly similar to those published in the most recent systematic review [17] although they are somewhat higher for hens’ egg (2.1 % compared to 0.0–1.7 %).

Novel to this study was the ability to look at risk factors for differing phenotypes of food hypersensitivity. Our exploratory analysis showed the factors associated with food hypersensitivity were wheeze, maternal atopy, gestation, age at first solids and healthy eating dietary pattern, which are similar to those found in previous research [18–25]. For IgE-mediated disease, the multivariable analysis demonstrated eczema, rhinitis and healthy eating pattern to be significant independent risk factors. The association between eczema and food allergy has long been recognised [26] and the opinion that eczema is a likely risk factor for food allergy is becoming more widely accepted due to data relating filaggrin gene defects with the development of eczema, allergic sensitization, and asthma and allergic rhinitis [27–29]. Filaggrin gene defect leads to a damaged skin barrier which increases permeability to exogenous proteins and possibly exposure of the innate immune system to allergens [30]. This phenomenon may also account for rhinitis being a risk factor for food allergy since the infant may also have become sensitised to aeroallergens through a damaged epithelial layer [31]. A healthy eating pattern was identified as being protective against the development of food allergy with the possible mechanism being the immunomodulatory effect of nutrients found in fruit and vegetables which were a feature of the observed healthy eating pattern along with a predominantly home-cooked diet [13]. Fruit and vegetables are good sources of vitamin C, beta-carotenes, folate and oligo-saccharides all of which have been shown to have immunomodulatory actions [32–34]. Also, home processed foods may have a higher microbial load than commercially prepared foods [35] and this may offer protection from the development of allergic disease as suggested by the “Hygiene Hypothesis” [36].

In the multivariable analysis for infants with non-IgE-mediated food hypersensitivity, dog in the home, healthy eating pattern, probiotic whilst breastfeeding and younger age at first solid food introduction were independent risk factors. The nature of the relationship between pet ownership and allergy development is still under debate [37–40]. If a protective effect is only seen for IgE-mediated conditions then that may explain the conflicting findings in the literature. It is recognised that pet ownership results in altered household microbial communities [41] and that these differences can lead to altered gut flora [42]. Whilst this may lead to changes in the immune system which reduce the risk of IgE-mediated allergy [43] this altered gut flora can adversely affect digestive enzyme activity, particularly of lactase. This is a previously reported phenomenon [44] and since the majority of infants with non-IgE-mediated food hypersensitivity were reactive to milk, this is a potential mechanism for these cases.

The effect of altered gut microbiota may also be the reason for other observed associations in these infants including healthy eating pattern and probiotic consumption during breastfeeding. The healthy eating dietary pattern may have a protective effect on gut health since it contained large amounts of home processed fruits and vegetables which are good sources of oligo-saccharides which, as naturally occurring prebiotics, promote gut colonization by bifidobacterium [45]. The observed association between probiotic consumption during breastfeeding and non-IgE-mediated food hypersensitivity is not readily explained but it can be hypothesised that it relates to the effect of the infant gut flora on gut enzyme activity. There is evidence that probiotics taken when breastfeeding alter breast milk composition [46] and that this may reduce the risk of allergy development in the infant [47]. However, there is no data describing the effect of maternal consumption of probiotic during lactation on the infant gut flora but it could be hypothesised that it increases the bifidobacteria colonisation that has been reported during breastfeeding [48] thus enhancing the effect of the breast milk on gut flora further. At breastfeeding cessation the infant’s gut flora becomes predominantly populated by coliform and bacteroid bacteria [48] which do not aid gut enzyme activity like hybridisable bacteria does [49] so the sudden change in the gut enzyme promoting environment may cause the observed Non-IgE mediated symptoms.

The age at first solid food introduction was significantly different for food hypersensitivity and for non-IgE-mediated food hypersensitivity. This observation could explain why some previous studies found an association between the early introduction of solids and food hypersensitivity [23, 24] and others have not [50, 51] since most studies do not identify the phenotype of hypersensitivity being investigated. It is considered that the infant gut is relatively immature before age 4–6 months and introducing solids before this time could cause food hypersensitivity symptoms, due to physiological mechanisms such as high intestinal permeability [52] which could upset the normal homeostasis of mucosal cell transport processes [53].

The strengths of this analysis include a large cohort of 1140 infants at general risk of developing food hypersensitivity with good follow-up to 24 months and a diagnosis using the gold standard methodology of a DBPCFC. Additionally, the methodology allowed for the prospective identification and clinical assessment of infants reacting to foods which reduced the likelihood of tolerance developing before a diagnosis could be confirmed. The prospective design also reduced the likelihood of recall bias during data collection and the prospective collection of food diary data is unique in a cohort of this size. Limitations of our analysis are that the study population is not fully representative of the population from which it was recruited since our mothers are older (Fig. 3). Also, the control infants were 5 months older than the cases as they were matched by birth but recruited after the cases were assessed; since control infants had never had any adverse reactions to food we do not expect this difference to impact on any of the factors included in the risk factor analyses. Additional limitations are that the numbers of infants diagnosed as reactive to foods were too small to enable all the likely risk factors to be detected, or to allow us to look at individual food reactions to determine whether different foods behave differently and have different risk factors associated with them. Also, despite the prospective nature of the study, reverse causality could not be completely avoided as clinical symptoms can lead to treatments which are subsequently associated with the condition in an analysis, as was the case for anti-reflux medication. Furthermore, a diagnosis of allergy can result in a change of behaviour as was the case for when mothers first introduced egg into the diet. However, where there was a suspicion of reverse causality, the variable was not included in the final multivariable analysis thus reducing its effect on the final study findings. Finally, the risk factor investigation represents an exploratory analysis and needs to be replicated, since possible regional differences within the UK may mean the findings from this study are not necessarily nationally representative.
Fig. 3
Fig. 3

Comparison between maternal age in UK birth cohort and similar populations. Percentage of mothers in each age range at enrolment into the UK birth cohort (PIFA) in comparison with England and Wales population; 2004 (E&W), 2005 infant feeding survey (IFS) and women delivering at Royal Hampshire County Hospital, Winchester (data from routine hospital data, 2007) (RHCH)

Conclusions

This study presents unique data from the UK on both IgE-mediated food allergy and non IgE-mediated food hypersensitivity in early childhood. It found the cumulative incidence of DBPCFC confirmed food hypersensitivity to be 5.0 % (3.7–6.7). Our results also suggest that different factors may affect the development of IgE-mediated and non-IgE-mediated reactions to food in infants and young children. However, it is important that this exploratory analysis is confirmed in other cohorts. Analysis of the EuroPrevall data from all the birth cohort centres for all food reactions can build upon this work and also investigate any geographical differences to food hypersensitivity reactions.

Abbreviations

aOR: 

adjusted odds ratio

DBPCFC: 

double blind placebo controlled food challenge

PIFA Study: 

prevalence of infant food allergy study

SPT: 

skin prick test

SpIgE: 

specific immunoglobulin E

WTCRF: 

Wellcome Trust Clinical Research Facility

Declarations

Authors’ contributions

KG was involved in writing the original study protocol, data collection, diagnosis of food allergy, statistical analysis and data management, drafted the initial manuscript and approved the final manuscript as submitted. TB was involved in statistical analysis and data management, revised the manuscript for important intellectual content and approved the final manuscript as submitted. EO was involved in data collection, diagnosis of food allergy, revised the manuscript for important intellectual content and approved the final manuscript as submitted. JM was involved in data collection, diagnosis of food allergy, revised the manuscript for important intellectual content and approved the final manuscript as submitted. JM was involved in statistical analysis and data management, revised the manuscript for important intellectual content and approved the final manuscript as submitted. TK was involved in recruitment, data collection, revised the manuscript for important intellectual content and approved the final manuscript as submitted. CM was involved in the conception and design of the original study protocol, revised the manuscript for important intellectual content and approved the final manuscript as submitted. KF was involved in the initiation and set up of the study, data collection, diagnosis of food allergy, revised the manuscript for important intellectual content and approved the final manuscript as submitted. BM was involved in the initiation and set up of the study, statistical analysis and interpretation of the data, revised the manuscript for important intellectual content and approved the final manuscript as submitted. KB was involved in the conception and design of the original study protocol, oversaw all EuroPrevall birth cohorts procedures, revised the manuscript for important intellectual content and approved the final manuscript as submitted. GR was involved in the initiation and set up of the study, data collection, diagnosis of food allergy, statistical analysis and interpretation of the data, revised the manuscript for important intellectual content and approved the final manuscript as submitted. All authors read and approved the final manuscript.

Acknowledgements

We thank all the families who took part in the PIFA study; the midwives of Winchester and Eastleigh Health Care Trust for their support of the study and help in recruitment; all the staff involved in the day-to-day running of the study; and the staff in Child Health and NIHR WTCRF at Southampton General Hospital for following up the participants and carrying out the clinical work establishing the diagnosis of food allergy. In particular, L. Gudgeon, R. King, J. Garland, E. Francis, S. Pestridge, K. Scally, E. Gatrell, L. Bellis, A. Acqua, and R. Kemp. Our thanks also to Professor Jonathan Hourihane for his crucial role in initially setting up the PIFA study.

Competing interests

K E. C. Grimshaw has received a grant and travel support from the UK Food Standards Agency and has previously had consultant arrangements with and received payment for lectures from Nutricia Ltd. J. Maskell has received a consulting fee/honorarium from the University of Southampton. E. M. Oliver has received travel support from the Food Standards Agency. G. Roberts has received a grant from the Food Standards Agency and was a member of the scientific advisory board for Danone Baby Nutrition. E.N.C. Mills has received grants from the European Commission. The rest of the authors declare that they have no competing interests.

Funding

Supported by the UK Food Standards Agency (Project TO7046) as part of the EU EuroPrevall Project (contract no. FOOD-CT-2005-514000).

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.

Authors’ Affiliations

(1)
Clinical and Experimental Sciences and Human Development in Health Academic Unit, Faculty of Medicine, University of Southampton, Mailpoint 803, Level F, South Academic Block, Southampton, SO16 6YD, UK
(2)
Department of Nutrition and Dietetics, Southampton Children’s Hospital, Southampton, SO16 6YD, UK
(3)
Primary Care and Population Sciences Academic Unit, Faculty of Medicine, University of Southampton, Southampton, SO16 6YD, UK
(4)
NIHR Clinical Research Facility, University Hospital Southampton NHS Foundation Trust, Southampton, SO16 6YD, UK
(5)
The Hampshire Hospitals Foundation Trust, Winchester, SO22 5DG, UK
(6)
Institute of Inflammation and Repair, Manchester Academic Health Science Centre, Manchester Institute of Biotechnology, The University of Manchester, Manchester, M1 7DN, UK
(7)
Department of Paediatric Pneumology and Immunology, Charité University Medical Centre, Berlin, Germany
(8)
NIHR Respiratory Biomedical Research Unit, University Hospital Southampton NHS Foundation Trust, Southampton, SO16 6YD, UK

References

  1. Flokstra-de Blok BM, Dubois AE, Vlieg-Boerstra BJ, Oude Elberink JN, Raat H, DunnGalvin A, et al. Health-related quality of life of food allergic patients: comparison with the general population and other diseases. Allergy. 2010;65(2):238–44.PubMedView ArticleGoogle Scholar
  2. Mackenzie H, Roberts G, Van LD, Dean T. A new quality of life scale for teenagers with food hypersensitivity. Pediatr Allergy Immunol. 2012;23(5):404–11.PubMedView ArticleGoogle Scholar
  3. Voordouw J, Fox M, Cornelisse J, Antonides G, Mugford M, Frewer L. Household costs associated with food allergy: an exploratory study. British Food Journal. 2010;112(11):1205–15.View ArticleGoogle Scholar
  4. Sladkevicius E, Nagy E, Lack G, Guest JF. Resource implications and budget impact of managing cow milk allergy in the UK. J Med Econ. 2010;13(1):119–28.PubMedView ArticleGoogle Scholar
  5. Nwaru BI, Hickstein L, Panesar SS, Muraro A, Werfel T, Cardona V, et al. The epidemiology of food allergy in Europe: a systematic review and meta-analysis. Allergy. 2014 (in press).Google Scholar
  6. Prescott SL, Pawankar R, Allen KJ, Campbell DE, Sinn JK, Fiocchi A, et al. A global survey of changing patterns of food allergy burden in children. World Allergy Organ J. 2013;6(1):21.PubMedPubMed CentralView ArticleGoogle Scholar
  7. Venter C, Hasan AS, Grundy J, Pereira B, Bernie CC, Voigt K, et al. Time trends in the prevalence of peanut allergy: three cohorts of children from the same geographical location in the UK. Allergy. 2010;65(1):103–8.PubMedView ArticleGoogle Scholar
  8. Ker J, Hartert TV. The atopic march: what’s the evidence? Ann Allergy Asthma Immunol. 2009;103(4):282–9.PubMedPubMed CentralView ArticleGoogle Scholar
  9. Dharmage SC, Lowe AJ, Matheson MC, Burgess JA, Allen KJ, Abramson MJ. Atopic dermatitis and the atopic march revisited. Allergy. 2013.Google Scholar
  10. Venter C, Pereira B, Voigt K, Grundy J, Clayton CB, Higgins B, et al. Factors associated with maternal dietary intake, feeding and weaning practices, and the development of food hypersensitivity in the infant. Pediatr Allergy Immunol. 2009;20(4):320–7.PubMedView ArticleGoogle Scholar
  11. McBride D, Keil T, Grabenhenrich L, Dubakiene R, Drasutiene G, Fiocchi A, et al. The EuroPrevall birth cohort study on food allergy: baseline characteristics of 12,000 newborns and their families from nine European countries. Pediatr Allergy Immunol. 2012;23(3):230–9.PubMedView ArticleGoogle Scholar
  12. Keil T, McBride D, Grimshaw K, Niggemann B, Xepapadaki P, Zannikos K, et al. The multinational birth cohort of EuroPrevall: background, aims and methods. Allergy. 2010;20(65):482–90.View ArticleGoogle Scholar
  13. Grimshaw KE, Maskell J, Oliver EM, Morris RC, Foote KD, Mills EN, et al. Diet and food allergy development during infancy: birth cohort study findings using prospective food diary data. J Allergy Clin Immunol. 2014;133(2):511–9.PubMedView ArticleGoogle Scholar
  14. Grimshaw KE, Maskell J, Oliver EM, Morris RC, Foote KD, Mills EN, et al. Introduction of complementary foods and the relationship to food allergy. Pediatrics. 2013;132(6):e1529–38.PubMedView ArticleGoogle Scholar
  15. Johansson SGO, Bieber T, Dahl R, Friedmann PS, Lanier BQ, Lockey RF, et al. Revised nomenclature for allergy for global use: report of the nomenclature review committee of the World Allergy Organization, October 2003. J Allergy Clin Immunol. 2004;113:832–6.PubMedView ArticleGoogle Scholar
  16. http://www.ats.ucla.edu/stat/stata/dae/exlogit.htm. Accessed 26 June 2015.
  17. Nwaru BI, Hickstein L, Panesar SS, Roberts G, Muraro A, Sheikh A. Prevalence of common food allergies in Europe: a systematic review and meta-analysis. Allergy. 2014.Google Scholar
  18. Burr ML, Limb ES, Maguire MJ, Amarah L, Eldridge BA, Layzell JC, et al. Infant feeding, wheezing, and allergy: a prospective study. Arch Dis Child. 1993;68(6):724–8.PubMedPubMed CentralView ArticleGoogle Scholar
  19. Hourihane JO, Dean TP, Warner JO. Peanut allergy in relation to heredity, maternal diet, and other atopic diseases: results of a questionnaire survey, skin prick testing, and food challenges. BMJ. 1996;313(7056):518–21.PubMedPubMed CentralView ArticleGoogle Scholar
  20. Ruiz RG, Kemeny DM, Price JF. Higher risk of infantile atopic dermatitis from maternal atopy than from paternal atopy. Clin Exp Allergy. 1992;22(8):762–6.PubMedView ArticleGoogle Scholar
  21. McKeever TM, Lewis SA, Smith C, Hubbard R. Mode of delivery and risk of developing allergic disease. J Allergy Clin Immunol. 2002;109(5):800–2.PubMedView ArticleGoogle Scholar
  22. Eggesbo M, Botten G, Stigum H, Nafstad P, Magnus P. Is delivery by cesarean section a risk factor for food allergy? J Allergy Clin Immunol. 2003;112(2):420–6.PubMedView ArticleGoogle Scholar
  23. Fergusson DM, Horwood LJ. Early solid food diet and eczema in childhood: a 10-year longitudinal study. Pediatr Allergy Immunol. 1994;5(6 Suppl):44–7.PubMedView ArticleGoogle Scholar
  24. Kajosaari M. Atopy prophylaxis in high-risk infants. Prospective 5-year follow-up study of children with six months exclusive breastfeeding and solid food elimination. Adv Exp Med Biol. 1991;310:453–8.PubMedView ArticleGoogle Scholar
  25. Nwaru BI, Takkinen HM, Niemela O, Kaila M, Erkkola M, Ahonen S, et al. Introduction of complementary foods in infancy and atopic sensitization at the age of 5 years: timing and food diversity in a Finnish birth cohort. Allergy. 2013;68(4):507–16.PubMedView ArticleGoogle Scholar
  26. Werfel T, Ballmer-Weber B, Eigenmann PA, Niggemann B, Rance F, Turjanmaa K, et al. Eczematous reactions to food in atopic eczema: position paper of the EAACI and GA2LEN. Allergy. 2007;62(7):723–8.PubMedView ArticleGoogle Scholar
  27. Palmer CN, Irvine AD, Terron-Kwiatkowski A, Zhao Y, Liao H, Lee SP, et al. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis. Nat Genet. 2006;38(4):441–6.PubMedView ArticleGoogle Scholar
  28. Marenholz I, Nickel R, Ruschendorf F, Schulz F, Esparza-Gordillo J, Kerscher T, et al. Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march. J Allergy Clin Immunol. 2006;118(4):866–71.PubMedView ArticleGoogle Scholar
  29. van den Oord RA, Sheikh A. Filaggrin gene defects and risk of developing allergic sensitisation and allergic disorders: systematic review and meta-analysis. BMJ. 2009;339:b2433.PubMedPubMed CentralView ArticleGoogle Scholar
  30. Jung T, Stingl G. Atopic dermatitis: therapeutic concepts evolving from new pathophysiologic insights. J Allergy Clin Immunol. 2008;122(6):1074–81.PubMedView ArticleGoogle Scholar
  31. Lack G. Epidemiologic risks for food allergy. J Allergy Clin Immunol. 2008;121(6):1331–6.PubMedView ArticleGoogle Scholar
  32. Rosenlund H, Kull I, Pershagen G, Wolk A, Wickman M, Bergstrom A. Fruit and vegetable consumption in relation to allergy: disease-related modification of consumption? J Allergy Clin Immunol. 2011;127(5):1219–25.PubMedView ArticleGoogle Scholar
  33. Hollingsworth JW, Maruoka S, Boon K, Garantziotis S, Li Z, Tomfohr J, et al. In utero supplementation with methyl donors enhances allergic airway disease in mice. J Clin Invest. 2008;118(10):3462–9.PubMedPubMed CentralGoogle Scholar
  34. Kukkonen K, Savilahti E, Haahtela T, Juntunen-Backman K, Korpela R, Poussa T, et al. Probiotics and prebiotic galacto-oligosaccharides in the prevention of allergic diseases: a randomized, double-blind, placebo-controlled trial. J Allergy Clin Immunol. 2007;119(1):192–8.PubMedView ArticleGoogle Scholar
  35. Randhawa S, Kakuda Y, Wong CL, Yeung DL. Microbial safety, nutritive value and residual pesticide levels are comparable among commercial, laboratory and homemade baby food samples—a pilot study. Open Nutr J. 2012;6:89–96.View ArticleGoogle Scholar
  36. Strachan DP. Hay fever, hygiene, and household size. BMJ. 1989;299(6710):1259–60.PubMedPubMed CentralView ArticleGoogle Scholar
  37. Gern JE, Reardon CL, Hoffjan S, Nicolae D, Li Z, Roberg KA, et al. Effects of dog ownership and genotype on immune development and atopy in infancy. J Allergy Clin Immunol. 2004;113(2):307–14.PubMedView ArticleGoogle Scholar
  38. Lodge CJ, Allen KJ, Lowe AJ, Hill DJ, Hosking CS, Abramson MJ, et al. Perinatal cat and dog exposure and the risk of asthma and allergy in the urban environment: a systematic review of longitudinal studies. Clin Dev Immunol. 2012;2012:176484.PubMedPubMed CentralView ArticleGoogle Scholar
  39. Lodrup Carlsen KC, Roll S, Carlsen KH, Mowinckel P, Wijga AH, Brunekreef B, et al. Does pet ownership in infancy lead to asthma or allergy at school age? Pooled analysis of individual participant data from 11 European birth cohorts. PLoS One. 2012;7(8):e43214.PubMedPubMed CentralView ArticleGoogle Scholar
  40. Park YB, Mo EK, Lee JY, Kim JH, Kim CH, Hyun IG, et al. Association between pet ownership and the sensitization to pet allergens in adults with various allergic diseases. Allergy Asthma Immunol Res. 2013;5(5):295–300.PubMedPubMed CentralView ArticleGoogle Scholar
  41. Fujimura KE, Johnson CC, Ownby DR, Cox MJ, Brodie EL, Havstad SL, et al. Man’s best friend? The effect of pet ownership on house dust microbial communities. J Allergy Clin Immunol. 2010;126(2):410–2.PubMedPubMed CentralView ArticleGoogle Scholar
  42. Nermes M, Niinivirta K, Nylund L, Laitinen K, Matomaki J, Salminen S, et al. Perinatal pet exposure, faecal microbiota, and wheezy bronchitis: is there a connection? ISRN Allergy. 2013;2013:827934.PubMedPubMed CentralView ArticleGoogle Scholar
  43. Campo P, Kalra HK, Levin L, Reponen T, Olds R, Lummus ZL, et al. Influence of dog ownership and high endotoxin on wheezing and atopy during infancy. J Allergy Clin Immunol. 2006;118(6):1271–8.PubMedPubMed CentralView ArticleGoogle Scholar
  44. Bampoe V, Sapsford RJ, Avigad S, Shiner M. Lactase degradation by human enteric bacteria. Lancet. 1979;2(8134):125–7.PubMedView ArticleGoogle Scholar
  45. Slavin J. Fiber and prebiotics: mechanisms and health benefits. Nutrients. 2013;5(4):1417–35.PubMedPubMed CentralView ArticleGoogle Scholar
  46. Prescott SL, Wickens K, Westcott L, Jung W, Currie H, Black PN, et al. Supplementation with Lactobacillus rhamnosus or Bifidobacterium lactis probiotics in pregnancy increases cord blood interferon-gamma and breast milk transforming growth factor-beta and immunoglobin A detection. Clin Exp Allergy. 2008;38(10):1606–14.PubMedView ArticleGoogle Scholar
  47. West CE, D’Vaz N, Prescott SL. Dietary immunomodulatory factors in the development of immune tolerance. Curr Allergy Asthma Rep. 2011;11(4):325–33.PubMedView ArticleGoogle Scholar
  48. Fanaro S, Chierici R, Guerrini P, Vigi V. Intestinal microflora in early infancy: composition and development. Acta Paediatr Suppl. 2003;91(441):48–55.PubMedGoogle Scholar
  49. Zhong Y, Priebe MG, Vonk RJ, Huang CY, Antoine JM, He T, et al. The role of colonic microbiota in lactose intolerance. Dig Dis Sci. 2004;49(1):78–83.PubMedView ArticleGoogle Scholar
  50. Zutavern A, von Mutius E, Harris J, Mills P, Moffatt S, White C, et al. The introduction of solids in relation to asthma and eczema. Arch Dis Child. 2004;89(4):303–8.PubMedPubMed CentralView ArticleGoogle Scholar
  51. Filipiak B, Zutavern A, Koletzko S, Von BA, Brockow I, Grubl A, et al. Solid food introduction in relation to eczema: results from a four-year prospective birth cohort study. J Pediatr. 2007;151(4):352–8.PubMedView ArticleGoogle Scholar
  52. Golden B. Nutrition in Infancy. In: Shetty P, editor. Nutrition through the life cycle. London: IBT Global; 2002. p. 15–36.View ArticleGoogle Scholar
  53. Fordtran JS. Speculations on the pathogenesis of diarrhoea. Federation Proceedings. 1967;26(5):1405–14.PubMedGoogle Scholar

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