Evidence map›Paper›PMID 27993387›Full record

Trial reportAtherosclerosis2017

Low vitamin D does not predict statin associated muscle symptoms but is associated with transient increases in muscle damage and pain.

Beth A Taylor, Lindsay Lorson, C Michael White, Paul D Thompson

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Atherosclerosis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.7field-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

7 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Management of patients with statin intolerance.Best practice & research. Clinical endocrinology & metabolism · 2023
    Review
  3. Article
  4. Observational
  5. Article
  6. Article
  7. Statin-Associated Muscle Disease: Advances in Diagnosis and Management.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Beth A TaylorDepartment of Kinesiology, University of Connecticut, Storrs, CT, 06269, USA; Division of Cardiology, Henry Low Heart Center, Hartford Hospital, Hartford, CT, 06102, USA; University of Connecticut School of Medicine, Farmington, CT, 06032, USA. Electronic address: Beth.Taylor@uconn.edu.
Lindsay LorsonDivision of Cardiology, Henry Low Heart Center, Hartford Hospital, Hartford, CT, 06102, USA.
C Michael WhiteUniversity of Connecticut School of Medicine, Farmington, CT, 06032, USA.
Paul D ThompsonDivision of Cardiology, Henry Low Heart Center, Hartford Hospital, Hartford, CT, 06102, USA; University of Connecticut School of Medicine, Farmington, CT, 06032, USA.
Hartford Hospital · USUniversity of Connecticut · US

Funding

CoEnzyme Q10 in Statin MyopathyRC1AT005836 · NCCIH · HARTFORD HOSPITAL · PI THOMPSON, PAUL DAVIS · 2009 to 2010
$865k
NCCIH NIH HHS RC1 AT005836
6 · The paper itself

Abstract

BACKGROUND AND

aimsLow vitamin D (VITD) may contribute to statin-associated muscle symptoms (SAMS). We examined the influence of baseline and change in VITD in patients with verified SAMS.

methodsSAMS was verified in 120 patients with prior statin muscle complaints using 8-week randomized, double-blind crossover trials of simvastatin (SIMVA) 20 mg/d and placebo. 25 (OH)vitamin D was measured at each phase of the trial.

resultsForty-three patients (35.8%) experienced muscle pain on SIMVA but not placebo, exhibiting confirmed SAMS. VITD (mean ± standard deviation) prior to SIMVA treatment was not different between patients who did (31.7 ± 12.1 ng/mL, n = 43) or did not (31.6 ± 10.3 ng/mL, n = 77) develop SAMS and did not predict SAMS (p = 0.96). The change in VITD with SIMVA treatment was not different between patients with and without SAMS (0.3 ± 5.9 vs. 0.2 ± 8.3 ng/mL, respectively) and did not predict SAMS (p = 0.96). The proportion of patients classified as VITD deficient (<20 ng/mL) did not differ between patients with (n = 16) and without (n = 10) SAMS (χ

conclusionsBaseline VITD, VITD deficiency/insufficiency and changes in VITD with statin therapy do not predict SAMS in patients with rigorously verified SAMS. However, low VITD may exacerbate statin-induced muscle injury and could contribute to SAMS development with a longer duration of statin treatment.

Indexed as

AgedBiomarkersCreatine KinaseCross-Over StudiesDouble-Blind MethodFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMiddle AgedMyalgiaRisk AssessmentRisk FactorsSimvastatinTime FactorsVitamin D25-hydroxyvitamin DBiomarkersCreatine KinaseHydroxymethylglutaryl-CoA Reductase InhibitorsSimvastatinVitamin DMuscle symptomsStatin myalgiaVitamin D deficiency

Identifiers

PMID27993387
PMCPMC6083851
OpenAlexW2554831534

What OpenQuestion holds

Textmetadata
LicenceTDM
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.