Evidence map›Paper›PMID 27620899›Full record

Trial reportPsychopharmacology2016

Incidence of non-alcoholic fatty liver disease and metabolic dysfunction in first episode schizophrenia and related psychotic disorders: a 3-year prospective randomized interventional study.

María José Morlán-Coarasa, María Teresa Arias-Loste, Víctor Ortiz-García de la Foz, Obdulia Martínez-García, Carmen Alonso-Martín, Javier Crespo, Manuel Romero-Gómez, Emilio Fábrega, Benedicto Crespo-Facorro

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Psychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 49 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

María José Morlán-CoarasaDepartment of Medicine and Psychiatry. Psychiatry Unit. IDIVAL, Instituto de Investigación Valdecilla, Hospital Universitario Marques de Valdecilla, 39008, Santander, Spain. josetamc@hotmail.com.
María Teresa Arias-LosteGastroenterology and Hepatology Department. Infection, Immunity and Digestive Pathology Group. IDIVAL, Instituto de Investigación Valdecilla, Hospital Universitario Marques de Valdecilla, 39008, Santander, Spain.
Víctor Ortiz-García de la FozDepartment of Medicine and Psychiatry. Psychiatry Unit. IDIVAL, Instituto de Investigación Valdecilla; Instituto de Salud Carlos III, 3-CIBERSAM, Centro Investigación Biomédica en Red Salud Mental, Hospital Universitario Marques de Valdecilla, 39008, Santander, Spain.
Obdulia Martínez-GarcíaDepartment of Medicine and Psychiatry. Psychiatry Unit. IDIVAL, Instituto de Investigación Valdecilla; Instituto de Salud Carlos III, 3-CIBERSAM, Centro Investigación Biomédica en Red Salud Mental, Hospital Universitario Marques de Valdecilla, 39008, Santander, Spain.
Carmen Alonso-MartínGastroenterology and Hepatology Department. Infection, Immunity and Digestive Pathology Group. IDIVAL, Instituto de Investigación Valdecilla, Hospital Universitario Marques de Valdecilla, 39008, Santander, Spain.
Javier CrespoGastroenterology and Hepatology Department. Infection, Immunity and Digestive Pathology Group. IDIVAL, Instituto de Investigación Valdecilla, Hospital Universitario Marques de Valdecilla, 39008, Santander, Spain.
Manuel Romero-GómezUCM Digestive Diseases and Ciberehd, University of Seville, Hospital Universitario de Valme, 41004, Sevilla, Spain.
Emilio FábregaGastroenterology and Hepatology Department. Infection, Immunity and Digestive Pathology Group. IDIVAL, Instituto de Investigación Valdecilla, Hospital Universitario Marques de Valdecilla, 39008, Santander, Spain.
Benedicto Crespo-FacorroDepartment of Medicine and Psychiatry. Psychiatry Unit. IDIVAL, Instituto de Investigación Valdecilla; Instituto de Salud Carlos III, 3-CIBERSAM, Centro Investigación Biomédica en Red Salud Mental, Hospital Universitario Marques de Valdecilla, 39008, Santander, Spain. benedicto.crespo@unican.es.
Instituto de Investigación Marqués de Valdecilla · ESInstituto de Salud Carlos III · ESHospital Universitario de Valme · ESMarqués de Valdecilla University Hospital · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationalePatients with schizophrenia spectrum disorders have increased morbidity and mortality, largely due to cardiovascular disease, which is associated with antipsychotic treatment.

objectivesBecause of the link between cardiometabolic risk, non-alcoholic fatty liver disease (NAFLD), and antipsychotics, we aimed to investigate the development of NAFLD during the first 3 years of antipsychotic treatment in first episode non-affective psychosis patients.

resultsA sample of 191 subjects was included in final analyses, randomly assigned to aripiprazole (N = 83), risperidone (N = 12), quetiapine (N = 46), and ziprasidone (N = 50). At intake, 180 patients were antipsychotic naïve. The NAFLD fibrosis score, FIB-4 score, and the fatty liver index (FLI) were calculated at baseline, at 3 months, and then yearly for 3 years. None of the patients showed significant liver fibrosis according to the mentioned scores at baseline, prior to randomization. At 3 years follow-up, 25.1 % individuals showed a FLI score ≥60, which is a predictor of steatosis. Of the individuals considered indeterminate at baseline, 64.7 % developed a FLI score ≥60 and only 16.6 % who had a FLI score <30 at baseline, showed a FLI score predictor of steatosis at endpoint. The FLI score ≥60 at endpoint was associated with an increase of more than 7 % of the body mass index (FLI score ≥ 60, 91.7 %; FLI < 60, 55.9 %; p < 0.001), increased triglyceride levels (FLI score ≥ 60, 54.2 %; FLI < 60, 5.6 %; p < 0.001), decreased HDL levels (FLI score ≥ 60, 41.7 %; FLI < 60, 17.5 %; p = 0.001), hypertension (FLI score ≥ 60, 19.5 %; FLI < 60, 4.5 %; p = 0.002), and waist circumference increase (steatosis 68.8 %; FLI < 60, 14.0 %; p < 0.001).

conclusionsOur results support the importance of assessing the potential development of NAFLD in schizophrenia spectrum patients receiving antipsychotic medication.

Indexed as

AdultAntipsychotic AgentsAripiprazoleFemaleHumansIncidenceMaleMetabolic DiseasesMiddle AgedNon-alcoholic Fatty Liver DiseasePiperazinesProspective StudiesPsychotic DisordersQuetiapine FumarateRisperidoneSchizophreniaAntipsychotic AgentsAripiprazolePiperazinesQuetiapine FumarateRisperidoneThiazolesziprasidoneAntipsychoticsCardiometabolic riskHepatic steatosisLipidsMetabolic syndromePsychosis

Identifiers

PMID27620899
OpenAlexW2519415457

What OpenQuestion holds

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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.