Evidence map›Paper›PMID 31370189›Full record

ArticleJournal of clinical medicine2019

Effects of SHBG rs1799941 Polymorphism on Free Testosterone Levels and Hypogonadism Risk in Young Non-Diabetic Obese Males.

Daniel Castellano-Castillo, José Luis Royo, Ana Martínez-Escribano, Lidia Sánchez-Alcoholado, María Molina-Vega, María Isabel Queipo-Ortuño, Maximiliano Ruiz-Galdon, Juan J Álvarez-Millán, Pablo Cabezas-Sanchez, Armando Reyes-Engel and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

13 authors at 4 institutions in 1 country.

Daniel Castellano-CastilloUnidad de Gestión Clínica de Endocrinología y Nutrición del Hospital Virgen de la Victoria, Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, 29010 Málaga, Spain.ORCID 0000-0001-8041-8244
José Luis RoyoDepartamento de Especialidades Quirúrgicas, Bioquímica e Inmunología, Universidad de Málaga, 29010 Málaga, Spain.
Ana Martínez-EscribanoDepartamento de Especialidades Quirúrgicas, Bioquímica e Inmunología, Universidad de Málaga, 29010 Málaga, Spain.
Lidia Sánchez-AlcoholadoUnidad de Gestión Clínica de Endocrinología y Nutrición del Hospital Virgen de la Victoria, Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, 29010 Málaga, Spain.
María Molina-VegaUnidad de Gestión Clínica de Endocrinología y Nutrición del Hospital Virgen de la Victoria, Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, 29010 Málaga, Spain.
María Isabel Queipo-OrtuñoCentro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y la Nutrición, CIBERobn, 28029 Madrid, Spain.ORCID 0000-0002-2867-0845
Maximiliano Ruiz-GaldonDepartamento de Especialidades Quirúrgicas, Bioquímica e Inmunología, Universidad de Málaga, 29010 Málaga, Spain.
Juan J Álvarez-MillánConsulting Químico Sanitario SL (CQS Lab), 28521 Madrid, Spain.
Pablo Cabezas-SanchezConsulting Químico Sanitario SL (CQS Lab), 28521 Madrid, Spain.
Armando Reyes-EngelDepartamento de Especialidades Quirúrgicas, Bioquímica e Inmunología, Universidad de Málaga, 29010 Málaga, Spain.
Francisco J TinahonesUnidad de Gestión Clínica de Endocrinología y Nutrición del Hospital Virgen de la Victoria, Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, 29010 Málaga, Spain. fjtinahones@hotmail.com.
Fernando CardonaUnidad de Gestión Clínica de Endocrinología y Nutrición del Hospital Virgen de la Victoria, Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, 29010 Málaga, Spain. fernandocardonadiaz@gmail.com.
José C Fernandez-GarciaUnidad de Gestión Clínica de Endocrinología y Nutrición del Hospital Virgen de la Victoria, Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, 29010 Málaga, Spain.ORCID 0000-0003-2229-8488
Centro de Investigación Biomédica en Red · ESUniversidad de Málaga · ESInstitut Químic de Sarrià · ESInstituto de Investigación Biomédica de Málaga · ES

Funding

Consejeria de Salud, Junta de Andalucia and co-funded by Fondo Europeo de Desarrollo Regional- FEDER SAS PI-0173-2013Formación del Profesorado Universitario (FPU) Program, co-funded by Fondo Europeo de Desarrollo Regional- FEDER FPU13/04211"Miguel Servet Type II" program, co-funded by the Fondo Europeo de Desarrollo Regional - FEDER CPI13/00003Nicolas Monardes Program, from Consejería de Salud, co-funded by the Fondo Europeo de Desarrollo Regional - FEDER C-0030-2018Nicolas Monardes Program, from Consejería de Salud, co-funded by the Fondo Europeo de Desarrollo Regional - FEDER C-0032-2016"Rio Hortega" Program, co-funded by Fondo Europeo de Desarrollo Regional- FEDER CM18/0120Servicio Andaluz de Salud, co-funded by Fondo Europeo de Desarrollo Regional- FEDER B-0003-2017
6 · The paper itself

Abstract

introductionObesity has been associated with increased risk of presenting hypogonadism. Free testosterone (FT) is the fraction of testosterone that carries out the biological function of testosterone, and is determined from total testosterone (TT) and sex-hormone binding globulin (SHBG) levels. We aimed to study the SHBG polymorphism rs1799941 in a cohort of young non-diabetic obese males to unravel the possible implication of this polymorphism in obesity-related hypogonadism. METHODOLOGY: 212 young (<45 years) non-diabetic obese (BMI ≥ 30 kg/m

resultsThe rs1799941 frequencies were different among the groups. Higher proportion of the allele (A) was found in HG, compared to EuG and normal FT HG. Among the genotypes, the rare homozygous (AA) were found in the normal FT HG group and higher levels of serum SHBG and lower of FT were observed. The presence of the allele A was related (according to lineal regression models) to an increased of SHBG levels ((GA) β = 3.28; (AA) β = 12.45) and a decreased of FT levels ((GA) β = -9.19; (AA) β = -18.52). The presence of the allele (A) increased the risk of presenting HG compared to normal FT HG (OR = 2.54).

conclusionsThe rs1799941 of the SHBG gene can partially determine the presence of obesity-related hypogonadism in young non-diabetic males and whether these subjects have normal FT HG.

Indexed as

free testosteronehypogonadismobesitypolymorphismrs1799941SHBG

Identifiers

PMID31370189
PMCPMC6722847
OpenAlexW2965175113

What OpenQuestion holds

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LicenceCC BY
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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.