Evidence map›Paper›PMID 37170809›Full record

ArticleThe Journal of clinical endocrinology and metabolism2023

Leptin and IGF-1 in Infancy Are Associated With Variants in DHCR7 and CYP2R1 That Relate With Type 1 Diabetes and 25OHD.

Antigoni Eleftheriou, Ken K Ong, Ieuan A Hughes, Clive J Petry

Open access · hybridAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 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
0.3field-weighted citation impact, top 42% 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, 1 citations in OpenAlex.

  1. Regulatory Mechanism ofBiomolecules · 2025
    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.

Antigoni EleftheriouDepartment of Paediatrics, University of Cambridge, Cambridge CB2 0QQ, UK.ORCID 0000-0003-1374-719X
Ken K OngDepartment of Paediatrics, University of Cambridge, Cambridge CB2 0QQ, UK.ORCID 0000-0003-4689-7530
Ieuan A HughesDepartment of Paediatrics, University of Cambridge, Cambridge CB2 0QQ, UK.ORCID 0000-0002-8787-1575
Clive J PetryDepartment of Paediatrics, University of Cambridge, Cambridge CB2 0QQ, UK.ORCID 0000-0002-6642-9825
University of Cambridge · GB

Funding

Department of HealthMedical Research Council 7500001180Medical Research Council G1001995Medical Research Council MC_UU_00006/2Medical Research Council MC_UU_12015/2Medical Research Council MR/K50127X/1Medical Research Council U106179472
6 · The paper itself

Abstract

contextVitamin D has been variably implicated in risk of developing type 1 diabetes based on cohorts of at-risk individuals. Emergent type 1 diabetes in childhood is putatively preceded by altered growth.

objectiveWe explored whether polymorphisms in vitamin D metabolism genes modify risk of type 1 diabetes via effects on growth in a prospective, population-based cohort of infants.

methodsThe Cambridge Baby Growth Study enrolled newborns from Cambridgeshire, UK, for follow-up in infancy. In 612 infants, we genotyped single nucleotide polymorphisms in vitamin D metabolism genes that relate with type 1 diabetes: rs10741657 and rs12794714 in CYP2R1, rs12785878 in DHCR7, and rs10877012 in CYP27B1. Multivariate linear regression analyses tested associations between genotypes and anthropometric indices (weight, length, and skinfold thickness) or growth-related hormones (C-peptide, IGF-1, and leptin) in infancy.

resultsBirth weight showed borderline associations with the diabetes risk-increasing alleles in CYP2R1, rs10741657 (β = -.11, P = .02) and rs12794714 (β = -.09, P = .04). The risk-increasing allele rs12794714 was also associated with higher IGF-1 levels at age 24 months (β = .30, P = .01). At age 3 months, the risk-increasing allele rs12785878 in DHCR7, known to negatively associate with 25-hydroxyvitamin D levels, showed a positive association with leptin levels (β = .23, P = .009), which was pronounced in girls (P = .004) vs boys (P = .7).

conclusionThe vitamin D metabolism genes DHCR7 and CYP2R1 might influence infancy leptin and IGF-1 levels respectively. These findings open the possibility for a developmental role of vitamin D that is mediated by growth-related hormones with implications for the onset of type 1 diabetes autoimmunity.

Indexed as

Diabetes Mellitus, Type 1Vitamin D DeficiencyChild, PreschoolCholestanetriol 26-MonooxygenaseCytochrome P450 Family 2FemaleGenetic Predisposition to DiseaseGenotypeHumansInfantInfant, NewbornInsulin-Like Growth Factor ILeptinMalePolymorphism, Single NucleotideProspective StudiesCholestanetriol 26-MonooxygenaseCYP2R1 protein, humanCytochrome P450 Family 2Insulin-Like Growth Factor ILeptinVitamin DVitaminsearly growthIGF-1leptintype 1 diabetesvitamin D

Identifiers

PMID37170809
PMCPMC10584008
OpenAlexW4376226188

What OpenQuestion holds

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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.