Evidence map›Paper›PMID 36323479›Full record

ArticleBMJ open2022

Influence of maternal body mass index on human milk composition and associations to infant metabolism and gut colonisation: MAINHEALTH - a study protocol for an observational birth cohort.

Katrine Overgaard Poulsen, Julie Astono, Rasmus Riemer Jakobsen, Niels Uldbjerg, Jens Fuglsang, Dennis Sandris Nielsen, Ulrik Kræmer Sundekilde

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05111990 (The Influence of Maternal Health on Human Breast Milk Composition With Potential Downstream Effects on Infant Metabolism and Gut Colonization), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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.

NCT05111990 active not recruitingnot on this map

The Influence of Maternal Health on Human Breast Milk Composition With Potential Downstream Effects on Infant Metabolism and Gut Colonization

TypeobservationalSponsorUniversity of AarhusRan2019 to 2028Enrolled168ConditionsBreast Milk Collection, Human Milk/Breastfeeding, Human Milk Microbiome, Infant Gut Microbiome
3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. 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

7 authors.

Katrine Overgaard PoulsenDepartment of Food Science, Aarhus University, Aarhus N, Denmark.ORCID 0000-0002-7478-3779
Julie AstonoDepartment of Food Science, Aarhus University, Aarhus N, Denmark.
Rasmus Riemer JakobsenDepartment of Food Science, University of Copenhagen, København, Denmark.ORCID 0000-0001-7416-1358
Niels UldbjergDepartment of Clinical Medicine, Aarhus University Hospital, Aarhus N, Denmark.
Jens FuglsangDepartment of Clinical Medicine, Aarhus University Hospital, Aarhus N, Denmark.
Dennis Sandris NielsenDepartment of Food Science, University of Copenhagen, København, Denmark.
Ulrik Kræmer SundekildeDepartment of Food Science, Aarhus University, Aarhus N, Denmark uksundekilde@food.au.dk.ORCID 0000-0003-4849-0996

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHuman milk provides all macronutrients for growth, bioactive compounds, micro-organisms and immunological components, which potentially interacts with and primes infant growth and, development, immune responses and the gut microbiota of the new-born. Infants with an overweight mother are more likely to become overweight later in life and overweight has been related to the gut microbiome. Therefore, it is important to investigate the mother-milk-infant triad as a biological system and if the maternal weight status influences the human milk composition, infant metabolism and gut microbiome. METHODS AND ANALYSIS: This study aims to include 200 mother-infant dyads stratified into one of three body mass index (BMI) categories based on mother's prepregnancy BMI. Multiomics analyses include metabolomics, proteomics, glycomics and microbiomics methods, aiming to characterise human milk from the mothers and further relate the composition to infant gut microbiota and its metabolic impact in the infant. Infant gut microbiota is analysed using 16S sequencing of faeces samples. Nuclear magnetic resonance and mass spectrometry are used for the remaining omics analysis. We investigate whether maternal pre-pregnancy BMI results in a distinct human milk composition that potentially affects the initial priming of the infant's gut environment and metabolism early in life. ETHICS AND DISSEMINATION: The Central Denmark Region Committees on Health Research Ethics has approved the protocol (J-nr. 1-10-72-296-18). All participants have before inclusion signed informed consent and deputy informed consent in accordance with the Declaration of Helsinki II. Results will be disseminated to health professionals including paediatricians, research community, nutritional policymakers, industry and finally the public. The scientific community will be informed via peer-reviewed publications and presentations at scientific conferences, the industry will be invited for meetings, and the public will be informed via reports in science magazines and the general press. Data cleared for personal data, will be deposited at public data repositories. TRIAL REGISTRATION NUMBER: Danish regional committee of the Central Jutland Region, journal number: 1-10-72-296-18, version 6.Danish Data Protection Agency, journal number: 2016-051-000001, 1304. CLINICALTRIALS: gov, identifier: NCT05111990.

Indexed as

Gastrointestinal MicrobiomeMilk, HumanBirth CohortBody Mass IndexFemaleHumansInfantObservational Studies as TopicOverweightPregnancymicrobiologynutrition & dieteticspaediatrics

Identifiers

PMID36323479
PMCPMC9639067

What OpenQuestion holds

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Registered trials

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.