Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/jspui/handle/10553/150654
Campo DC Valoridioma
dc.contributor.authorMasete, Matladien_US
dc.contributor.authorDias, Stephanieen_US
dc.contributor.authorMalaza, Nompumeleloen_US
dc.contributor.authorAdam, Sumaiyaen_US
dc.contributor.authorMutavhatsindi, Hygonen_US
dc.contributor.authorValverde-Tercedor, Carmenen_US
dc.contributor.authorVega Guedes, Begoñaen_US
dc.contributor.authorWägner, Anna Maria Claudiaen_US
dc.contributor.authorPheiffer, Carmenen_US
dc.date.accessioned2025-10-27T14:26:54Z-
dc.date.available2025-10-27T14:26:54Z-
dc.date.issued2025en_US
dc.identifier.issn1661-6596en_US
dc.identifier.otherWoS-
dc.identifier.otherScopus-
dc.identifier.urihttps://accedacris.ulpgc.es/jspui/handle/10553/150654-
dc.description.abstractDiabetes in pregnancy increases the risk of adverse perinatal outcomes for mother and child, with severity influenced by the type of diabetes and degree of hyperglycemia. This study aimed to identify circulating microRNAs (miRNAs) associated with different types of diabetes in pregnancy. Serum miRNAs were profiled in pregnant South African women with type 1 diabetes (T1DM), type 2 diabetes (T2DM), gestational diabetes (GDM), and normoglycemia using PCR arrays (n = 15). Differentially expressed miRNAs were validated in pregnant South African women (n = 167), and a separate cohort of Spanish pregnant women with T1DM and T2DM (n = 48). PCR arrays showed significant differential expression for miR-19b-3p (down arrow 9.8-fold; p = 0.033) in GDM, miR-20a-5p (down arrow 4.5-fold; p = 0.047) in T1DM, and miR-29a-3p (up arrow 1.8-fold; p = 0.002) in T2DM compared to normoglycemia. Screening in the larger cohort showed lower expression of miR-20a-5p (down arrow 2-fold; p = 0.013) in GDM and miR-30d-5p (down arrow 2.1-fold; p = 0.032) in T1DM compared to normoglycemia. Additionally, miR-20a-5p levels were higher in women with T2DM compared to those with GDM (up arrow 2.5-fold; p = 0.019). Our findings show that miRNA profiles are largely consistent across different types of diabetes in pregnancy, suggesting that hyperglycemia plays a key role in shaping miRNA expressions. Moreover, the identification of several shared gene targets suggests common underlying pathophysiological mechanisms.en_US
dc.languageengen_US
dc.relation.ispartofInternational Journal of Molecular Sciencesen_US
dc.sourceInternational Journal Of Molecular Sciences[ISSN 1661-6596],v. 26 (19), (Septiembre 2025)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320102 Genética clínicaen_US
dc.subject320108 Ginecologíaen_US
dc.subject.otherInsulin-Resistanceen_US
dc.subject.otherExpressionen_US
dc.subject.otherHyperglycemiaen_US
dc.subject.otherInflammationen_US
dc.subject.otherMirnasen_US
dc.subject.otherType 1 Diabetesen_US
dc.subject.otherType 2 Diabetesen_US
dc.subject.otherGestational Diabetesen_US
dc.subject.otherPregnancyen_US
dc.titleCirculating MicroRNA Profiles in Pregnant South African Women with Different Types of Diabetes Mellitusen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/ijms26199337en_US
dc.identifier.scopus105018892261-
dc.identifier.isi001593624000001-
dc.contributor.orcid0000-0001-5444-1395-
dc.contributor.orcid0000-0003-3008-4279-
dc.contributor.orcid0000-0002-6566-3425-
dc.contributor.orcid0000-0001-8769-3273-
dc.contributor.orcid0000-0001-6605-6275-
dc.contributor.orcid0000-0002-2003-246X-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0002-7663-9308-
dc.contributor.orcid0000-0002-0707-1552-
dc.contributor.authorscopusid57863193800-
dc.contributor.authorscopusid57194203430-
dc.contributor.authorscopusid57221745341-
dc.contributor.authorscopusid23099047900-
dc.contributor.authorscopusid57209304988-
dc.contributor.authorscopusid55208194600-
dc.contributor.authorscopusid56244156700-
dc.contributor.authorscopusid7401456520-
dc.contributor.authorscopusid7801368756-
dc.identifier.eissn1422-0067-
dc.identifier.issue19-
dc.relation.volume26en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.description.numberofpages16en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Masete, M-
dc.contributor.wosstandardWOS:Dias, S-
dc.contributor.wosstandardWOS:Malaza, N-
dc.contributor.wosstandardWOS:Adam, S-
dc.contributor.wosstandardWOS:Mutavhatsindi, H-
dc.contributor.wosstandardWOS:Valverde-Tercedor, C-
dc.contributor.wosstandardWOS:Vega-Guedes, B-
dc.contributor.wosstandardWOS:Wägner, AM-
dc.contributor.wosstandardWOS:Pheiffer, C-
dc.date.coverdateSeptiembre 2025en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,179
dc.description.jcr4,9
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.miaricds10,8
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptGIR IUIBS: Diabetes y endocrinología aplicada-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptGIR IUIBS: Diabetes y endocrinología aplicada-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-7663-9308-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameVega Guedes, Begoña-
crisitem.author.fullNameWägner, Anna Maria Claudia-
Colección:Artículos
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