Evidence map›Paper›PMID 27667144›Full record

ArticleAtencion primaria2017

[Lixisenatide in patients with type 2 diabetes and obesity: Beyond glycaemic control].

M Mar Roca-Rodríguez, María Teresa Muros de Fuentes, Gonzalo Piédrola-Maroto, Miguel Quesada-Charneco, Silvia Maraver-Selfa, Francisco J Tinahones, Isabel Mancha-Doblas

Open access · goldAbstract read
In one paragraph

Article in Atencion primaria, 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
0.2field-weighted citation impact, top 33% 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, 8 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

7 authors at 5 institutions in 1 country.

M Mar Roca-RodríguezUGC de Endocrinología y Nutrición, Hospital Universitario Puerta del Mar, Cádiz, España. Electronic address: maroca80@gmail.com.
María Teresa Muros de FuentesUGC de Endocrinología y Nutrición, Hospital Virgen de las Nieves, Granada, España.
Gonzalo Piédrola-MarotoUGC de Endocrinología y Nutrición, Hospital Virgen de las Nieves, Granada, España.
Miguel Quesada-CharnecoUGC de Endocrinología y Nutrición, Hospital San Cecilio, Granada, España.
Silvia Maraver-SelfaUGC de Endocrinología y Nutrición, Hospital Clínico Universitario Virgen de la Victoria y Hospital Regional Universitario, Málaga, España.
Francisco J TinahonesUGC de Endocrinología y Nutrición, Hospital Clínico Universitario Virgen de la Victoria y Hospital Regional Universitario, Málaga, España; Instituto de Investigación Biomédica de Málaga (IBIMA), Complejo Hospitalario de Málaga (Virgen de la Victoria)/Universidad de Málaga; CIBER Pathophysiology of Obesity and Nutrition (CB06/03), Málaga, España.
Isabel Mancha-DoblasUGC de Endocrinología y Nutrición, Hospital Clínico Universitario Virgen de la Victoria y Hospital Regional Universitario, Málaga, España.
Hospital Clínico Universitario Virgen de la Victoria · ESHospital Universitario Virgen de las Nieves · ESHospital Universitario Puerta del Mar · ESInstituto de Investigación Biosanitaria de Granada · ESSpanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo evaluate tolerance to lixisenatide and its effects on weight and metabolic control in type2 diabetes and obese patients.

designProspective study.

settingEndocrinology clinics in Almeria, Granada and Malaga.

participantsPatients with type2 diabetes and obesity.

interventionsResponse and tolerance to lixisenatide treatment. MAIN MEASUREMENTS: Clinical and analytical data of the subjects were evaluated at baseline and after treatment.

resultsThe study included 104 patients (51% women) with type2 diabetes and obesity (Almeria 18.3%; Granada 40.4%; Malaga 41.3%). The mean age was 58.4±10.5years, and the mean duration of diabetes was 11.2±6.7years. The patients were re-evaluated at 3.8±1.6months after treatment with lixisenatide. Significant improvements were found in weight (P<.001), body mass index (P<.001), waist circumference (P=.002), systolic blood pressure (P<.001), diastolic blood pressure (P=.001), fasting glucose (P<.001), HbA1c (P=.022), Total cholesterol (P<.001), LDL-cholesterol (P=.046), triglycerides (P=.020), hypertension drugs (P<.001), and lipids drugs (P<.001). No changes were observed in levels of amylase related to lixisenatide treatment, and 7.9% of patients did not tolerate it.

conclusionsLixisenatide achieved significant improvements in anthropometric parameters, glycaemic control (fasting glucose and HbA1c), blood pressure and lipids. It was safe and well tolerated in most patients. In addition, there was a significant increase in the use of antihypertensive and lipid-lowering therapy.

Indexed as

AdultBlood GlucoseDiabetes Mellitus, Type 2FemaleGlucagon-Like Peptide-2 ReceptorHumansHypoglycemic AgentsMiddle AgedObesityPeptidesProspective StudiesBlood GlucoseGlucagon-Like Peptide-2 ReceptorHypoglycemic AgentslixisenatidePeptidesAnálogos de GLP-1Control metabólicoDiabetes tipo2GLP-1LixisenatidaLixisenatideMetabolic controlObesidadObesityType 2 diabetes

Identifiers

PMID27667144
PMCPMC6875984
OpenAlexW2524569815

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.