Evidence map›Paper›PMID 35883228›Full record

ArticleThe Journal of nutrition2022

Unique Metabolic Profiles Associate with Gestational Diabetes and Ethnicity in Low- and High-Risk Women Living in the UK.

Harriett Fuller, Mark Iles, J Bernadette Moore, Michael A Zulyniak

Open access · hybridAbstract read
In one paragraph

Article in The Journal of nutrition, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Observational
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  11. Multigenerational diabetes mellitus.Frontiers in endocrinology · 2023
    Review
  12. 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

4 authors at 1 institution in 1 country.

Harriett FullerNutritional Epidemiology Group, School of Food Science and Nutrition, University of Leeds, Leeds, UK.ORCID 0000-0001-8381-519X
Mark IlesLeeds Institute of Medical Research, University of Leeds, Leeds, UK.ORCID 0000-0002-2603-6509
J Bernadette MooreNutritional Epidemiology Group, School of Food Science and Nutrition, University of Leeds, Leeds, UK.ORCID 0000-0003-4750-1550
Michael A ZulyniakNutritional Epidemiology Group, School of Food Science and Nutrition, University of Leeds, Leeds, UK.ORCID 0000-0003-4944-5521
University of Leeds · GB

Funding

Medical Research Council MC_UU_00,011/6Medical Research Council MC_UU_00011/6Wellcome TrustWellcome Trust 217446/Z/19/Z
6 · The paper itself

Abstract

backgroundGestational diabetes mellitus (GDM) is the most common global pregnancy complication; however, prevalence varies substantially between ethnicities, with South Asians (SAs) experiencing up to 3 times the risk of the disease compared with white Europeans (WEs). Factors driving this discrepancy are unclear, although the metabolome is of great interest as GDM is known to be characterized by metabolic dysregulation.

objectivesThe primary aim was to characterize and compare the metabolic profiles of GDM in SA and WE women (at <28 wk of gestation) from the Born in Bradford (BIB) prospective birth cohort in the United Kingdom.

methodsIn total, 146 fasting serum metabolites, from 2,668 pregnant WE and 2,671 pregnant SA women (average BMI 26.2 kg/m2, average age 27.3 y) were analyzed using partial least squares discriminatory analyses to characterize GDM status. Linear associations between metabolite values and post-oral glucose tolerance test measures of dysglycemia (fasting glucose and 2 h postglucose) were also examined.

resultsSeven metabolites associated with GDM status in both ethnicities (variable importance in projection ≥1), whereas 6 additional metabolites associated with GDM only in WE women. Unique metabolic profiles were observed in healthy-weight women who later developed GDM, with distinct metabolite patterns identified by ethnicity and BMI status. Of the metabolite values analyzed in relation to dysglycemia, lactate, histidine, apolipoprotein A1, HDL cholesterol, and HDL2 cholesterol associated with decreased glucose concentration, whereas DHA and the diameter of very low-density lipoprotein particles (nm) associated with increased glucose concertation in WE women, and in SAs, albumin alone associated with decreased glucose concentration.

conclusionsThis study shows that the metabolic risk profile for GDM differs between WE and SA women enrolled in BiB in the United Kingdom. This suggests that etiology of the disease differs between ethnic groups and that ethnic-appropriate prevention strategies may be beneficial.

Indexed as

Diabetes, GestationalAdultAlbuminsApolipoprotein A-IBlood GlucoseCholesterol, HDLEthnicityFemaleGlucoseHistidineHumansLactatesLipoproteins, LDLMetabolomePregnancyProspective StudiesAlbuminsApolipoprotein A-IBlood GlucoseCholesterol, HDLGlucoseHistidineLactatesLipoproteins, LDLethnicityGDMmaternal healthmetabolomicspersonalized nutritionPLSDApregnancySouth AsianssPLSDA

Identifiers

PMID35883228
PMCPMC9535440
OpenAlexW4288040227

What OpenQuestion holds

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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.