Evidence map›Paper›PMID 35072787›Full record

ArticleEuropean journal of nutrition2022

Human milk fatty acid composition and its association with maternal blood and adipose tissue fatty acid content in a cohort of women from Europe.

Francesca Giuffrida, Mathilde Fleith, Amélie Goyer, Tinu Mary Samuel, Isabelle Elmelegy-Masserey, Patric Fontannaz, Cristina Cruz-Hernandez, Sagar K Thakkar, Cathriona Monnard, Carlos Antonio De Castro and 15 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of nutrition, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 55 citations in OpenAlex.

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  13. [Mammary epithelial cells from women synthetize omega-3 and 6 fatty acids].Revista medica del Instituto Mexicano del Seguro Social · 2025
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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

25 authors at 13 institutions in 9 countries.

Francesca GiuffridaNestlé Research, Vers-chez les-Blanc, 1000, Lausanne 26, Switzerland. francesca.giuffrida@rdls.nestle.com.ORCID http://orcid.org/0000-0002-9816-3814
Mathilde FleithNestlé Research, Vers-chez les-Blanc, 1000, Lausanne 26, Switzerland.
Amélie GoyerNestlé Research, Vers-chez les-Blanc, 1000, Lausanne 26, Switzerland.
Tinu Mary SamuelNestlé Product Technology Center-Nutrition, Société des Produits Nestlé S.A., 1800, Vevey, Switzerland.
Isabelle Elmelegy-MassereyNestlé Research, Vers-chez les-Blanc, 1000, Lausanne 26, Switzerland.
Patric FontannazNestlé Research, Vers-chez les-Blanc, 1000, Lausanne 26, Switzerland.
Cristina Cruz-HernandezNestlé Research, Vers-chez les-Blanc, 1000, Lausanne 26, Switzerland.
Sagar K ThakkarNestlé Research, 29 Quality Road, Singapore, 618802, Singapore.
Cathriona MonnardNestlé Research, Vers-chez les-Blanc, 1000, Lausanne 26, Switzerland.
Carlos Antonio De CastroNestlé Research, 29 Quality Road, Singapore, 618802, Singapore.
Luca LavalleNestlé Research, Vers-chez les-Blanc, 1000, Lausanne 26, Switzerland.
Thameur RakzaCentre d'Investigation Clinique de Lille, Hôpital Jeanne de Flandre, 59777, Lille, France.
Massimo AgostiOspedale del Ponte, Varese, Italy.
Isam Al-JashiPrivate Med. Practice, Bucharest, Romania.
Almerinda Barroso PereiraHospital de São Marcos, 4700-327, Braga, Portugal.
Maria Jose CosteiraICVS (Population Health Assessment)-Minho Medical School, Braga, Portugal.
Giovanna MarchiniKarolinska University Hospital, Stockholm, Sweden.
Mireille VanpeeKarolinska University Hospital, Stockholm, Sweden.
Tom StirisOslo University Hospital, Oslo, Norway.
Sylvia StoicescuPolizu Hospital, Bucharest, Romania.
Maria Gorett SilvaHospital de S. João, 4200-319, Porto, Portugal.
Jean-Charles PicaudHospices Civils de Lyon, Neonatology, Hôpital de La Croix Rousse, Hospices civils de Lyon, 69004, Lyon, France.
Cecilia Martinez-CostaHospital Clínico Universitario, University of Valencia, Valencia, Spain.
Magnus DomellöfDepartment of Clinical Sciences/Pediatrics, Umeå University, Umeå, Sweden.
Claude BilleaudNeonatology & Nutrition, CIC Pédiatrique 1401 Inserm, CHU de Bordeaux, Bordeaux, France.
Nestlé (Switzerland) · CHClinical Emergency Hospital Bucharest · ROKarolinska University Hospital · SENestlé (Singapore) · SGHôpital Jeanne de Flandre · FRHospital de São João · PTHospital de São Marcos · PTInserm · FROslo University Hospital · NOOspedale Filippo Del Ponte Varese · ITUmeå University · SEUniversitat de València · ESUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeHuman milk (HM) composition is influenced by factors, like maternal diet and body stores, among other factors. For evaluating the influence of maternal fatty acid (FA) status on milk FA composition, the correlation between FA content in HM and in maternal plasma, erythrocytes, and adipose tissue was investigated.

methods223 European women who delivered at term, provided HM samples over first four months of lactation. Venous blood and adipose tissue (only from mothers who consented and underwent a C-section delivery) were sampled at delivery. FAs were assessed in plasma, erythrocytes, adipose tissue, and HM. Evolution of HM FAs over lactation and correlations between FA content in milk and tissues and between mother's blood and cord blood were established.

resultsDuring lactation, arachidonic acid (ARA) and docosahexaenoic acid (DHA) significantly decreased, while linoleic acid (LA), alpha-linolenic acid (ALA), and eicosapentaenoic acid (EPA) remained stable. Positive correlations were observed between HM and adipose tissue for palmitic, stearic, oleic, and polyunsaturated fatty acids (PUFAs). Correlations were found between milk and plasma for oleic, LA, ARA, ALA, DHA, monounsaturated fatty acids (MUFAs), and PUFAs. No correlation was observed between erythrocytes and HM FAs. LA and ALA were more concentrated in maternal blood than in infant blood, contrary to ARA and DHA, supporting that biomagnification of LCPUFAs may have occurred during pregnancy.

conclusionsThese data show that maternal adipose tissue rather than erythrocytes may serve as reservoir of PUFAs and LCPUFAs for human milk. Plasma also supplies PUFAs and LCPUFAs to maternal milk. If both, adipose tissue and plasma PUFAs, are reflection of dietary intake, it is necessary to provide PUFAs and LCPUFAs during pregnancy or even before conception and lactation to ensure availability for mothers and enough supply for the infant via HM.

Indexed as

Fatty AcidsMilk, HumanAdipose TissueArachidonic AcidBreast FeedingDocosahexaenoic AcidsFatty Acids, UnsaturatedFemaleHumansInfantLactationLinoleic AcidPregnancyArachidonic AcidDocosahexaenoic AcidsFatty AcidsFatty Acids, UnsaturatedLinoleic AcidAdipose tissueDHAErythrocytesFatty acidsHuman milkLactationLCPUFALipidsNutritionPlasmaPregnancy

Identifiers

PMID35072787
PMCPMC9106604
OpenAlexW4207076142

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.