Evidence map›Paper›PMID 28796426›Full record

ArticleAmerican journal of medical genetics. Part A2017

Vitamin D levels in Smith-Lemli-Opitz syndrome.

Miyad Movassaghi, Simona Bianconi, Richard Feinn, Christopher A Wassif, Forbes D Porter

Abstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Review
  5. Review
  6. Review
  7. An Update on Vitamin D Metabolism.International journal of molecular sciences · 2020
    Review
  8. Review
  9. Article
  10. Disruption ofBone research · 2020
    Article
  11. Vitamin D Metabolism Revised: Fall of Dogmas.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    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

5 authors at 2 institutions in 1 country.

Miyad MovassaghiFrank H. Netter MD School of Medicine at Quinnipiac University, North Haven, Connecticut.ORCID http://orcid.org/0000-0002-3705-5764
Simona BianconiEunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health, Bethesda, Maryland.
Richard FeinnFrank H. Netter MD School of Medicine at Quinnipiac University, North Haven, Connecticut.
Christopher A WassifEunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health, Bethesda, Maryland.
Forbes D PorterEunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health, Bethesda, Maryland.
National Institutes of Health · USQuinnipiac University · US

Funding

Clinical Investigations of Smith-Lemli-Opitz SyndromeZIAHD008825 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI PORTER, FORBES · 2009 to 2019
$2.2M
Intramural NIH HHS Z99 HD999999
6 · The paper itself

Abstract

Smith-Lemli-Opitz syndrome (SLOS) is an autosomal recessive congenital malformation syndrome caused by mutations in the 7-dehydrocholesterol reductase gene. This inborn error of cholesterol synthesis leads to elevated concentrations of 7-dehydrocholesterol (7-DHC). 7-DHC also serves as the precursor for vitamin D synthesis. Limited data is available on vitamin D levels in individuals with SLOS. Due to elevated concentrations of 7-DHC, we hypothesized that vitamin D status would be abnormal and possibly reach toxic levels in patients with SLOS. Through a retrospective analysis of medical records between 1998 and 2006, we assessed markers of vitamin D and calcium metabolism from 53 pediatric SLOS patients and 867 pediatric patients who were admitted to the NIH Clinical Center (NIHCC) during the same time period. SLOS patients had significantly higher levels of 25(OH)D (48.06 ± 19.53 ng/ml, p < 0.01) across all seasons in comparison to the NIHCC pediatric patients (30.51 ± 16.14 ng/ml). Controlling for season and age of blood draw, 25(OH)D levels were, on average, 15.96 ng/ml (95%CI 13.95-17.90) higher in SLOS patients. Although, mean calcium values for both patient cohorts never exceeded the normal clinical reference range (8.6-10.2 mg/dl), the levels were higher in the SLOS cohort (9.49 ± 0.56 mg/dl, p < 0.01) compared to the NIHCC patients (9.25 ± 0.68 mg/dl). Overall, in comparison to the control cohort, individuals with SLOS have significantly higher concentrations of 25(OH)D that may be explained by elevated concentrations of serum 7-DHC. Despite the elevated vitamin D levels, there was no laboratory or clinical evidence of vitamin D toxicity.

Indexed as

AdolescentChildChild, PreschoolDehydrocholesterolsFemaleHumansInfantInfant, NewbornLongitudinal StudiesMaleOxidoreductases Acting on CH-CH Group DonorsPrognosisRetrospective StudiesSmith-Lemli-Opitz SyndromeVitamin D7-dehydrocholesterol7-dehydrocholesterol reductaseDehydrocholesterolsOxidoreductases Acting on CH-CH Group DonorsVitamin D7-dehydrocholesterolmetabolic disorderSmith-Lemli-Opitz syndromevitamin D

Identifiers

PMID28796426
PMCPMC5603413
OpenAlexW2745106268

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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.