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dc.contributor.author SOSA GARCIA, BETSY CORINA
dc.contributor.author HINOJOSA JUAREZ, ARACELI CONSUELO
dc.contributor.author GARCIA GARCIA, MARIA DEL CARMEN
dc.contributor.author PEREZ AMADO, CARLOS JHOVANI
dc.contributor.author JIMENEZ MORALES, SILVIA
dc.contributor.author Mendieta Zerón, Hugo
dc.creator SOSA GARCIA, BETSY CORINA; 701232
dc.creator HINOJOSA JUAREZ, ARACELI CONSUELO; 97918
dc.creator GARCIA GARCIA, MARIA DEL CARMEN; 1052
dc.creator PEREZ AMADO, CARLOS JHOVANI; 821714
dc.creator JIMENEZ MORALES, SILVIA; 38343
dc.creator Mendieta Zerón, Hugo; 45175
dc.date.accessioned 2022-07-05T02:52:49Z
dc.date.available 2022-07-05T02:52:49Z
dc.date.issued 2022-04-27
dc.identifier.issn 2589-8310
dc.identifier.uri http://hdl.handle.net/20.500.11799/113191
dc.description.abstract Introduction: The adipose tissue secretes chemerin and omentin related to metabolic diseases. It has been reported that both proteins encoded by retinoic acid receptor responder protein 2 (RARRES2) and intelectin‑1 (ITLN1) genes, respectively, are abnormally expressed in gestational diabetes mellitus (GDM). Aim: To evaluate the expression of these genes in visceral adipose tissue in pregnant women with GDM. Methods: Descriptive cross‑sectional study, with two groups, (A) GDM and (B) control group (pregnant women without GDM). Body mass index (BMI), blood pressure, lipids, and glucose were measured. RARRES2 and ITLN1 mRNA expression were evaluated using quantitative real‑time Reverse transcription‑polymerase chain reaction using TaqMan probes. Statistical analysis was performed using Kolmogórov–Smirnov, Pearson‑Spearman correlation, Kruskal–Wallis tests, and R language with Shapiro–Wilk, SPSS V21.0. Results: Sixty‑six women were included. Women with normal weight were more frequent in the control group (33.3%) than GDM (15.2%); overweight was similar in both groups (45.5%), and obesity was less common in the control group (21.2%) than GDM (39.3%). No differential expression of RARRES2 and ITLN1 genes among cases and controls were found, but RARRES2 expression differed (P = 0.016) between normal‑weight and overweight women in the control group, and ITLN1 expression significantly differed (P = 0.002) between overweight and obese women in the GDM group. Conclusions: ITLN1 could have a role in the GDM severity based on the BMI of the patients. es
dc.description.sponsorship Betsy Corina Sosa García received a scholarship from the National Council of Science and Technology (CONACYT)‑Mexico. es
dc.language.iso eng es
dc.publisher Wolters Kluwer - Medknow es
dc.rights openAccess es
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0 es
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0
dc.subject Retinoic Acid Receptor Responder Protein 2 es
dc.subject Intelectin‑1 es
dc.subject Visceral Adipose Tissue es
dc.subject Pregnant Women es
dc.subject Gestational Diabetes Mellitus es
dc.subject.classification MEDICINA Y CIENCIAS DE LA SALUD es
dc.subject.classification MEDICINA Y CIENCIAS DE LA SALUD
dc.title Retinoic Acid Receptor Responder Protein 2 and Intelectin‑1 in Visceral Adipose Tissue from Pregnant Women with Gestational Diabetes Mellitus es
dc.type Artículo es
dc.provenance Científica es
dc.road Dorada es
dc.organismo Medicina es
dc.ambito Internacional es
dc.audience students es
dc.audience researchers es
dc.type.conacyt article
dc.identificator 3


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  • Título
  • Retinoic Acid Receptor Responder Protein 2 and Intelectin‑1 in Visceral Adipose Tissue from Pregnant Women with Gestational Diabetes Mellitus
  • Autor
  • SOSA GARCIA, BETSY CORINA
  • HINOJOSA JUAREZ, ARACELI CONSUELO
  • GARCIA GARCIA, MARIA DEL CARMEN
  • PEREZ AMADO, CARLOS JHOVANI
  • JIMENEZ MORALES, SILVIA
  • Mendieta Zerón, Hugo
  • Fecha de publicación
  • 2022-04-27
  • Editor
  • Wolters Kluwer - Medknow
  • Tipo de documento
  • Artículo
  • Palabras clave
  • Retinoic Acid Receptor Responder Protein 2
  • Intelectin‑1
  • Visceral Adipose Tissue
  • Pregnant Women
  • Gestational Diabetes Mellitus
  • Los documentos depositados en el Repositorio Institucional de la Universidad Autónoma del Estado de México se encuentran a disposición en Acceso Abierto bajo la licencia Creative Commons: Atribución-NoComercial-SinDerivar 4.0 Internacional (CC BY-NC-ND 4.0)

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