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Family history of atopy in infants with cow's milk protein allergy: A French population-based study
N Kalach1, M Bellaïche2, I Elias-Billon3
1Clinique pédiatrique Saint-Antoine, hôpital Saint-Vincent-de-Paul, groupement des hôpitaux de l'institut catholique de Lille (GHICL), boulevard de Belfort, 59020 Lille cedex, France.
Insights
Infants diagnosed with cow's milk protein allergy (CMPA) frequently have a family history of atopy, particularly in first-degree relatives. This highlights the importance of considering family history in diagnosing CMPA in infants.
Area of Science:
- Pediatrics
- Allergology
- Genetics
Background:
- Cow's milk protein allergy (CMPA) is a common condition in infants.
- Family history of atopy is a known risk factor for allergic diseases.
Purpose of the Study:
- To describe the prevalence of family history of atopy in infants with CMPA.
- To analyze diagnostic approaches for CMPA in a real-world setting.
Main Methods:
- A French multicenter, cross-sectional, observational study.
- 1674 infants with suspected CMPA were enrolled by 466 private physicians.
- Family history of atopy was defined by parental report of atopy in first- or second-degree relatives.
Main Results:
- A family history of atopy was more common in infants with probable or documented CMPA (86% of cases).
- Digestive (92%) and skin (61%) symptoms were most frequent.
- Atopy in a parent was more frequent in infants with early-onset CMPA symptoms.
Conclusions:
- The study confirms a high rate of family history of atopy in infants with CMPA.
- Family history is a significant factor in the context of CMPA diagnosis.
Objectives:
This French multicenter, cross-sectional, observational study aimed to describe the family history of atopy in infants with cow's milk protein allergy (CMPA), and the related diagnostic approaches used by specialists in a real-life ambulatory setting.
Patients And Methods:
In total, 1674 infants with suspected CMPA [median age 4.5 months (range: 0.1-18.0), males 54%] were enrolled in the study by 466 private physicians (pediatricians: 97%). Family history of atopy was defined as a known history of atopy in at least one first- (father, mother, and/or sibling) and/or second-degree relative (grandparents, uncles, and aunts), as reported by parents to physicians.
Results:
Atopy in a first-degree relative was more common among infants with documented or high probability of CMPA (in 84% and 80% of cases, respectively, vs. the other subgroups, P=0.005). Most infants experienced digestive (92%) and skin (61%) symptoms suggestive of CMPA. Delayed reactions were reported in 64% of infants. According to a post-classification based on the results of previous diagnostic tests and procedures, 1133 infants (68%) had highly probable (52%) or documented CMPA (16%). In these infants, a history of atopy was reported in first- and/or second-degree relative(s) in 86% of cases (81% in first-degree relatives). Whatever the family history of atopy, the characteristics of the infants were similar, except for fewer pets in the case of negative family atopy (14% vs. 25%, P<0.001). Atopy in a parent was more frequent in infants who presented with the first signs suggestive of CMPA within the first 6 months of life vs. those with later first symptoms (75% vs. 65%, P=0.063).
Conclusion:
This French study confirms the high rate of family history of atopy in first-degree relatives of infants with probable or documented CMPA.
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