Evidence map›Paper›PMID 27077659›Full record

ArticlePloS one2016

Serum 25-Hydroxyvitamin D Status and Longitudinal Changes in Weight and Waist Circumference: Influence of Genetic Predisposition to Adiposity.

Sofus C Larsen, Lars Ängquist, Max Moldovan, Ville Huikari, Sylvain Sebert, Alana Cavadino, Tarunveer Singh Ahluwalia, Tea Skaaby, Allan Linneberg, Lise Lotte N Husemoen and 9 more

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Observational
  5. Low vitamin D status and obesity: Role of nutritionist.Reviews in endocrine & metabolic disorders · 2017
    Review
  6. 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

19 authors.

Sofus C LarsenResearch unit for Dietary Studies, the Parker Institute, Frederiksberg and Bispebjerg Hospitals, The Capital Region, Frederiksberg, Denmark.
Lars ÄngquistInstitute of Preventive Medicine, Bispebjerg and Frederiksberg Hospitals, the Capital Region, Copenhagen, Denmark.
Max MoldovanCentre for Population Health Research, School of Health Sciences and Sansom Institute, University of South Australia, Adelaide, Australia.
Ville HuikariCenter for Life-Course Health Research, Faculty of Medicine, P.O.Box 5000, FI-90014 University of Oulu, Oulu, Finland.
Sylvain SebertCenter for Life-Course Health Research, Faculty of Medicine, P.O.Box 5000, FI-90014 University of Oulu, Oulu, Finland.
Alana CavadinoCentre for Environmental and Preventive Medicine, Wolfson Institute of Preventive Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Tarunveer Singh AhluwaliaThe Novo Nordisk Foundation Center for Basic Metabolic Research, Section of Metabolic Genetics, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Tea SkaabyResearch Centre for Prevention and Health, Capital Region of Denmark, Copenhagen, Denmark.
Allan LinnebergResearch Centre for Prevention and Health, Capital Region of Denmark, Copenhagen, Denmark.
Lise Lotte N HusemoenResearch Centre for Prevention and Health, Capital Region of Denmark, Copenhagen, Denmark.
Ulla ToftResearch Centre for Prevention and Health, Capital Region of Denmark, Copenhagen, Denmark.
Oluf PedersenThe Novo Nordisk Foundation Center for Basic Metabolic Research, Section of Metabolic Genetics, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Torben HansenThe Novo Nordisk Foundation Center for Basic Metabolic Research, Section of Metabolic Genetics, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Karl-Heinz HerzigInstitute of Biomedicine, University of Oulu, Oulu, Finland.
Marjo-Riitta JarvelinCenter for Life-Course Health Research, Faculty of Medicine, P.O.Box 5000, FI-90014 University of Oulu, Oulu, Finland.
Chris PowerPopulation, Policy and Practice, UCL Institute of Child Health, University College London, London, United Kingdom.
Elina HyppönenCentre for Population Health Research, School of Health Sciences and Sansom Institute, University of South Australia, Adelaide, Australia.
Berit L HeitmannResearch unit for Dietary Studies, the Parker Institute, Frederiksberg and Bispebjerg Hospitals, The Capital Region, Frederiksberg, Denmark.
Thorkild I A SørensenInstitute of Preventive Medicine, Bispebjerg and Frederiksberg Hospitals, the Capital Region, Copenhagen, Denmark.

Funding

Type 1 Diabetes Genetics ConsortiumU01DK062418 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI RICH, STEPHEN S. · 2002 to 2007
$59.8M
Medical Research Council G0000934Medical Research Council G1001799Medical Research Council MR/N01104X/1NIDDK NIH HHS U01 DK062418Wellcome TrustWellcome Trust 068545/Z/02Wellcome Trust 076113
6 · The paper itself

Abstract

Studies of the relationship between serum 25-hydroxyvitamin D (25(OH)D) and changes in measures of adiposity have shown inconsistent results, and interaction with genetic predisposition to obesity has rarely been examined. We examined whether 25(OH)D was associated with subsequent annual changes in body weight (ΔBW) or waist circumference (ΔWC), and whether the associations were modified by genetic predisposition to a high BMI, WC or waist-hip ratio adjusted for BMI (WHRBMI). The study was based on 10,898 individuals from the Danish Inter99, the 1958 British Birth Cohort and the Northern Finland Birth Cohort 1966. We combined 42 adiposity-associated Single Nucleotide Polymorphisms (SNPs) into four scores indicating genetic predisposition to BMI, WC and WHRBMI, or all three traits combined. Linear regression was used to examine the association between serum 25(OH)D and ΔBW or ΔWC, SNP-score × 25(OH)D interactions were examined, and results from the individual cohorts were meta-analyzed. In the meta-analyses, we found no evidence of an association between 25(OH)D and ΔBW (-9.4 gram/y per 10 nmol/L higher 25(OH)D [95% CI: -23.0, +4.3; P = 0.18]) or ΔWC (-0.06 mm/y per 10 nmol/L higher 25(OH)D [95% CI: -0.17, +0.06; P = 0.33]). Furthermore, we found no statistically significant interactions between the four SNP-scores and 25(OH)D in relation to ΔBW or ΔWC. Thus, in view of the narrow CIs, our results suggest that an association between 25(OH)D and changes in measures of adiposity is absent or marginal. Similarly, the study provided evidence that there is either no or very limited dependence on genetic predisposition to adiposity.

Indexed as

Polymorphism, Single NucleotideAdiposityAgedBody Mass IndexBody WeightCohort StudiesDenmarkFemaleFinlandGenetic Association StudiesGenetic Predisposition to DiseaseHumansMaleMeta-Analysis as TopicMiddle AgedTime Factors25-hydroxyvitamin DVitamin D

Identifiers

PMID27077659
PMCPMC4831693

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Registered trials

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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.