Evidence map›Paper›PMID 38102583›Full record

Observational studyBMC pediatrics2023

A cross-sectional study on stool- and gastrointestinal-related outcomes of Mexican infants consuming different formulae.

Carlijn M Maasakkers, Jeske H J Hageman, Olivia Balcazar Muñoz, Tomás Gómez Tamayo, Andrés Blanco Montero, Luis Gerardo Garza Lara, Regina Flores-López, Miriam Contreras Fernández, Sofía Morán Ramos, Tim T Lambers

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMC pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.3field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Carlijn M MaasakkersFrieslandCampina, Amersfoort, The Netherlands.
Jeske H J HagemanFrieslandCampina, Amersfoort, The Netherlands.
Olivia Balcazar MuñozClínica Pediátrica Pigüi, Hospital Español, Mexico City, Mexico.
Tomás Gómez TamayoClínica VITALI, Guadalajara, Jalisco, Mexico.
Andrés Blanco MonteroClínica Pediátrica Pigüi, Hospital Español, Mexico City, Mexico.
Luis Gerardo Garza LaraClínica VITALI, Guadalajara, Jalisco, Mexico.
Regina Flores-LópezUnidad de Genómica de Poblaciones, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
Miriam Contreras FernándezFrieslandCampina, Amersfoort, The Netherlands.
Sofía Morán RamosUnidad de Genómica de Poblaciones, Instituto Nacional de Medicina Genómica, Mexico City, Mexico.
Tim T LambersFrieslandCampina, Amersfoort, The Netherlands. tim.lambers@frieslandcampina.com.
FrieslandCampina (Netherlands) · NLHospital Español · MXNational Institute of Genomic Medicine · MXWageningen University & Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmaturities present at birth, such as in the gut microbiome and digestive, nervous, and immune system, resolve with time. Nevertheless, this may result in mild digestive symptoms early in life, particularly in formula-fed infants. Formula composition and processing may impact this discomfort. This study therefore aimed to assess stool characteristics and gastrointestinal symptoms of healthy infants fed different formulae.

methodsA multicenter, cross-sectional, observational trial was performed in Mexico between November 2019 and January 2022, where exclusively formula-fed infants (n = 342, aged 1-4 months) were studied in four groups based on their existing formula use. Feeding was continued per practice following label instructions. For 7 days, parents/caregivers were requested to record fecal characteristics, using the Amsterdam Infant Stool Scale, and rate gastrointestinal symptoms. Stool samples were collected to determine pH, dry matter content, and fecal calprotectin levels.

resultsMost infants had a soft/formed stool consistency, although odds for hard stools were different between groups. Gastrointestinal symptom scores revealed significant differences for burping and diarrhea, while other symptoms did not differ between groups. No significant differences between groups were found for stool frequency, dry matter content, and fecal pH. Although calprotectin was within the expected healthy ranges, significant differences among groups were seen. Furthermore, calprotectin significantly correlated with the severity of the gastrointestinal symptoms burping, flatulence, abdominal distension, and diarrhea.

conclusionsDifferences in stool characteristics and specific differences in gastrointestinal symptoms were observed between different formula brand users. This may potentially be explained by the different composition and processing of the formulae, although there are multiple factors that influence the assessed outcomes.

trial registrationThe study was registered in the Netherlands Trial Registry (NL7805), linked to https://trialsearch.who.int/ , on 11/06/2019.

Indexed as

Gastrointestinal DiseasesCross-Sectional StudiesDiarrheaDouble-Blind MethodFecesHumansInfantInfant FormulaLeukocyte L1 Antigen ComplexMexicoLeukocyte L1 Antigen ComplexDigestive symptomsFecal characteristicsInfant formulaInfant nutrition

Identifiers

PMID38102583
PMCPMC10722798
OpenAlexW4389793186

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.