Evidence map›Paper›PMID 35382499›Full record

ArticleJournal of the Endocrine Society2022

The Arg82Cys Polymorphism of the Protein Nepmucin Implies a Role in HDL Metabolism.

Sophia Metz, Nikolaj T Krarup, Thomas Bryrup, Julie Støy, Ehm A Andersson, Christina Christoffersen, Matt J Neville, Malene R Christiansen, Anna E Jonsson, Daniel R Witte and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the Endocrine Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

18 authors at 4 institutions in 2 countries.

Sophia MetzNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-5871-9892
Nikolaj T KrarupNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.
Thomas BryrupNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.
Julie StøyAarhus University Hospital, Steno Diabetes Center Aarhus, 8200 Aarhus, Denmark.
Ehm A AnderssonNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.
Christina ChristoffersenDepartment of Clinical Biochemistry, Rigshospitalet, 2100 Copenhagen, Denmark.
Matt J NevilleOxford Centre for Diabetes, Endocrinology & Metabolism, OX3 7LE Oxford, UK.
Malene R ChristiansenNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-9772-3576
Anna E JonssonNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.
Daniel R WitteDepartment of Public Health, Section of Epidemiology, Aarhus University, 8000 Aarhus, Denmark.
Ulla KampmannAarhus University Hospital, Steno Diabetes Center Aarhus, 8200 Aarhus, Denmark.
Lars B NielsenDepartment of Clinical Biochemistry, Rigshospitalet, 2100 Copenhagen, Denmark.
Niklas R JørgensenDepartment of Clinical Biochemistry, Rigshospitalet, 2100 Copenhagen, Denmark.
Fredrik KarpeOxford Centre for Diabetes, Endocrinology & Metabolism, OX3 7LE Oxford, UK.
Niels GrarupNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-5526-1070
Oluf PedersenNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-3321-3972
Tuomas O KilpeläinenNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-8349-3028
Torben HansenNovo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-8748-3831
University of Copenhagen · DKAarhus University · DKChurchill Hospital · GBSteno Diabetes Centers · DK

Funding

Wellcome Trust 090532Wellcome Trust 098381
6 · The paper itself

Abstract

Context: Blood lipid levels are linked to the risk of cardiovascular disease and regulated by genetic factors. A low-frequency polymorphism Arg82Cys (rs72836561) in the membrane protein nepmucin, encoded by Objective: Here, we augment the genetic effect of Arg82Cys on fasting plasma concentrations of HDL subclasses, postprandial lipemia after a standardized high-fat meal, and glycemic status to further untangle its role in HDL metabolism. Methods: We elucidated fasting associations with HDL subclasses in a population-based cohort study (Oxford BioBank, OBB), including 4522 healthy men and women. We investigated fasting and postprandial consequences on HDL metabolism in recall-by-genotype (RbG) studies (fasting: 20 carrier/20 noncarrier; postprandial: 7 carrier/17 noncarrier), and shed light on the synergistic interaction with glycemic status. Results: A lower fasting plasma concentration of cholesterol in large HDL particles was found in healthy male carriers of the Cys82 polymorphism compared to noncarriers, both in the OBB ( Conclusion: Taken together, our results indicate an association between the Arg82Cys variant and a lower concentration of HDL particles and HDLc, especially in larger HDL subclasses, suggesting a link between nepmucin and HDLc metabolism or maturation.

Indexed as

apolipoproteinscholesterol transporthuman geneticslipid metabolismmetabolismtriglycerides

Identifiers

PMID35382499
PMCPMC8974852
OpenAlexW4214869554

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.