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dc.contributor.authorOnat, Altan
dc.contributor.authorKaya, Aysem
dc.contributor.authorSIMSEK, Baris
dc.contributor.authorCan, Gunay
dc.contributor.authorAdemoglu, Evin
dc.contributor.authorKaradeniz, Yusuf
dc.contributor.authorUZUN, Ahmet Okan
dc.date.accessioned2021-03-05T18:15:14Z
dc.date.available2021-03-05T18:15:14Z
dc.date.issued2018
dc.identifier.citationOnat A., Ademoglu E., Karadeniz Y., Can G., UZUN A. O. , SIMSEK B., Kaya A., "Population-based serum omentin-1 levels: paradoxical association with cardiometabolic disorders primarily in men", BIOMARKERS IN MEDICINE, cilt.12, ss.141-149, 2018
dc.identifier.issn1752-0363
dc.identifier.otherav_c9788957-90ee-449a-8451-5b94473f9c81
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/133493
dc.identifier.urihttps://doi.org/10.2217/bmm-2017-0197
dc.description.abstractAim: The conflicting relationships of serum omentin with inflammation markers and cardiometabolic disorders were investigated. Results & methods: Unselected 864 population-based middle-aged adults were cross-sectionally studied by sex-specific omentin tertiles. Men in the lowest omentin tertile (T1) had lower systolic blood pressure, HbA1c and glucose values and tended in T3 to higher lipoprotein(a) levels. Logistic regression analysis, adjusted for four covariates, revealed significant independent associations with the presence of hypertension and diabetes only in men. Sex-and age-adjusted odds ratio in gender combined for T2 & T3 versus T1 was 1.34 (95% CI: 1.00-1.79) for metabolic syndrome. Discussion & conclusion: The elicited adverse relationships of omentin-1 support the notion of oxidative stress-induced proinflammatory conversion of omentin, rendering loss of anti-inflammatory properties.
dc.language.isoeng
dc.subjectTıbbi Ekoloji ve Hidroklimatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, ARAŞTIRMA VE DENEYSEL
dc.titlePopulation-based serum omentin-1 levels: paradoxical association with cardiometabolic disorders primarily in men
dc.typeMakale
dc.relation.journalBIOMARKERS IN MEDICINE
dc.contributor.departmentAtatürk Üniversitesi , ,
dc.identifier.volume12
dc.identifier.issue2
dc.identifier.startpage141
dc.identifier.endpage149
dc.contributor.firstauthorID54742


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