Clinical Response to Two Formulas in Infants with Parent-Reported Signs of Formula Intolerance: A Multi-Country, Double-Blind, Randomized Trial

Boosba Vivatvakin; Elvira Estorninos; Reyin Lien; Hung Chang Lee; Kam Lun Ellis Hon; Jowena Lebumfacil; Colin I Cercamondi; Sheri Volger

doi:10.1177/2333794X20954332

Clinical Response to Two Formulas in Infants with Parent-Reported Signs of Formula Intolerance: A Multi-Country, Double-Blind, Randomized Trial

Glob Pediatr Health. 2020 Sep 25:7:2333794X20954332. doi: 10.1177/2333794X20954332. eCollection 2020.

Authors

Boosba Vivatvakin¹, Elvira Estorninos², Reyin Lien³, Hung Chang Lee⁴, Kam Lun Ellis Hon⁵, Jowena Lebumfacil⁶, Colin I Cercamondi⁷, Sheri Volger⁷

Affiliations

¹ Chulalongkorn University, Bangkok, Thailand.
² Asian Hospital and Medical Center, Muntinlupa City, Philippines.
³ Chang Gung Memorial Hospital, Taoyuan, Taiwan.
⁴ Mackay Memorial Hospital, Taipei, Taiwan.
⁵ The Chinese University of Hong Kong, Shatin, N.T., Hong Kong.
⁶ Wyeth Nutrition, Makati City, Manila, Philippines.
⁷ Nestlé Product Technology Center - Nutrition, Société des Produits Nestlé S.A., Vevey, Switzerland.

Abstract

Background: Signs of feeding intolerance are common in formula-fed infants. We evaluated the clinical response to a partially hydrolyzed 100% whey protein formula with high sn-2 palmitate and reduced lactose (FA) and to an alpha-lactalbumin-enriched whey-predominant intact protein formula with full lactose (FB) in healthy full-term infants with parent-reported signs of feeding intolerance.

Methods: In a double-blind, parallel-group trial in 6 Asian study centers, exclusively formula-fed infants aged 30 to 90 days, whose parents reported fussiness-crying for ≥2 hours/day plus gassiness and/or stooling difficulty, and intended to switch formula, were randomly assigned to FA (n = 130) or FB (n = 129) for 14 days. Primary endpoint was daily duration of fussiness-crying. Secondary endpoints included gassiness, spitting-up, vomiting, sleep pattern, Infant Gastrointestinal Symptom Questionnaire (IGSQ) Index, infant temperament and maternal anxiety.

Results: Mean ± SE minutes/day of fussiness-crying in the 256 analyzed infants (FA, n = 127 and FB, n = 129) substantially decreased from baseline to study end in FA (291 ± 14 to 140 ± 8; -52%, P < .001), and FB (313 ± 14 to 153 ± 11, -51%, P < .001) with no difference between groups. Similarly, gassiness, spitting-up, vomiting and sleep pattern significantly improved by study end for both formulas. Mean ± SE IGSQ index scores significantly decreased from baseline to study end (FA: 44.5 ± 0.9 to 28.6 ± 0.7; FB: 44.5 ± 0.8 to 29.0 ± 0.7; P < .001) with no differences between groups. Infant temperament and maternal anxiety also improved significantly in both groups by study end.

Conclusion: Switching from standard, full-lactose, intact whey/casein infant formulas to either study formula resulted in an improvement of gastrointestinal symptoms and associated behaviors in infants with signs of feeding intolerance.

Trial registration: https://clinicaltrials.gov, NCT02021058.

Keywords: Feeding intolerance; crying; formula switch; fussiness; gastrointestinal symptoms and associated behaviors.

Associated data

ClinicalTrials.gov/NCT02021058