Evidence map›Paper›PMID 28950844›Full record

Trial reportBMC women's health2017

Effect of simvastatin on monocyte chemoattractant protein-1 expression in endometriosis patients: a randomized controlled trial.

Wanwisa Waiyaput, Somphoch Pumipichet, Sawaek Weerakiet, Sasivimol Rattanasiri, Areepan Sophonsritsuk

Abstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in BMC women's health, 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
–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

7 citing papers in PubMed.

  1. Article
  2. Review
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  5. Review
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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.

Wanwisa WaiyaputOffice of Research Academic and Innovation, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Somphoch PumipichetDepartment of Obstetrics and Gynecology, Faculty of Medicine Srinakharinwirot University, Bangkok, Thailand.
Sawaek WeerakietReproductive Endocrinology and Infertility Unit, Department of Obstetrics & Gynecology, Ramathibodi Hospital, Mahidol University, Rama VI Rd, Bangkok, 10400, Thailand.
Sasivimol RattanasiriSection for Clinical Epidemiology and Biostatistics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Areepan SophonsritsukReproductive Endocrinology and Infertility Unit, Department of Obstetrics & Gynecology, Ramathibodi Hospital, Mahidol University, Rama VI Rd, Bangkok, 10400, Thailand. areepan.sop@mahidol.ac.th.ORCID http://orcid.org/0000-0002-4589-0030

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSimvastatin is a promising new drug for the treatment of endometriosis. It is a cholesterol-lowering drug that acts by inhibiting HMG-CoA reductase, resulting in a decrease in mevalonate, a precursor of cholesterol and monocyte chemoattractant protein-1 (MCP-1). This study investigated the effect of pre-operative oral simvastatin administration on MCP-1 gene expression and serum MCP-1 protein levels in patients with endometriosis.

methodsA prospective, randomized, controlled study was conducted at the Reproductive Endocrinology Unit of the Department of Obstetrics and Gynecology at the Faculty of Medicine Ramathibodi Hospital. Forty women (mean age: 18-45 years) scheduled for laparoscopic surgery who had been diagnosed with endometriosis were recruited and randomly assigned to either a treatment group (20 mg/d of orally administered simvastatin for 2 weeks before surgery) or an untreated control group. Serum was collected before and after treatment and protein levels of MCP-1 were determined. MCP-1 and CD68 transcript levels were also quantified using real-time PCR on endometriotic cyst tissues.

resultsMCP-1 gene expression on endometriotic cyst was not significantly different between the simvastatin-treated and untreated groups (P = 0.99). CD68 expression was higher in the treatment group compared to the control group, but this was not statistically significant (P = 0.055). Serum MCP-1 levels following simvastatin treatment were higher than in samples obtained before treatment (297.89 ± 70.77 and 255.51 ± 63.79 pg/ml, respectively) (P = 0.01).

conclusionsTreatment with 20 mg/d of simvastatin for 2 weeks did not reduce the expression of either the chemokine MCP-1 gene or macrophage-specific genes. Cumulatively, this suggests that simvastatin is not ideal for treating endometriosis because a higher dose of simvastatin (40-100 mg/d) would be needed to achieve the target outcome, which would significantly increase the risk of myopathy in patients.

trial registrationThai Clinical Trials Registry TCTR20130627003 Registered: June 27, 2013.

Indexed as

AdolescentAdultChemokine CCL2EndometriosisFemaleGene ExpressionHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMiddle AgedProspective StudiesSimvastatinYoung AdultCCL2 protein, humanChemokine CCL2Hydroxymethylglutaryl-CoA Reductase InhibitorsSimvastatinEndometriosisLaparoscopyMCP-1 gene expressionSerum MCP-1Simvastatin

Identifiers

PMID28950844
PMCPMC5615793

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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.