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http://hdl.handle.net/11452/24973
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DC Field | Value | Language |
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dc.date.accessioned | 2022-03-14T07:59:04Z | - |
dc.date.available | 2022-03-14T07:59:04Z | - |
dc.date.issued | 2004-11 | - |
dc.identifier.citation | Ersoy, C. vd. (2004). “Effect of amlodipine on insulin resistance & tumor necrosis factor-alpha levels in hypertensive obese type 2 diabetic patients”. Indian Journal of Medical Research, 120(5), 481-488. | en_US |
dc.identifier.issn | 0971-5916 | - |
dc.identifier.uri | http://hdl.handle.net/11452/24973 | - |
dc.description.abstract | Background & objectives: Tumour necrosis factor-alpha (TNF-α) has been suggested to play a key role in insulin resistance (IR) in obesity and may contribute to the development of type 2 diabetes mellitus. Recently, studies are focused on the effect of antihypertensive drugs on insulin sensitivity and cytokines. We undertook this study to evaluate the effect of amlodipine, a long-acting dihydropyridine calcium channel blocker treatment on TNF-α, homeostasis model assessment (HOMA) IR and leptin levels in obese hypertensive type 2 diabetic patients. Methods: Amlodipine 5-10 mg for 12 wk was given to type 2 diabetic patients in the amiodipine group. Pre- and post-treatment values of laboratory parameters in the amlodipine group were compared with those of normotensive nondiabetic obese controls. At baseline blood pressures (BP) and metabolic parameters were measured in all patients and repeated after 12 wk in the amlodipine group. Results: Basal waist-to-hip ratio, systolic and diastolic BPs, fasting glucose, TNF-α and HOMA-IR values of the amlodipine group were higher than the control group. No difference was detected in body mass index, fasting insulin, hemoglobin Alc and leptin values between groups. The systolic and diastolic BPs, fasting glucose, HOMA-IR and TNF-α values decreased significantly after the treatment. But, there was no correlation between percentage change in TNF-α and HOMA-IR. Interpretation & conclusion: Besides reducing BP, amlodipine seemed to improve IR and decrease TNF-α levels. In this context, these properties may provide additional benefits of antihypertensive drug regimens chosen for this population, but larger group interventions are needed. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wolters Kluwer Medknow Publications | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Immunology | en_US |
dc.subject | General and internal medicine | en_US |
dc.subject | Research and experimental medicine | en_US |
dc.subject | Amlodipine | en_US |
dc.subject | Insulin resistance | en_US |
dc.subject | Leptin | en_US |
dc.subject | Tumor necrosis factor-alpha | en_US |
dc.subject | Serum-levels | en_US |
dc.subject | Plasma | en_US |
dc.subject | Sensitivity | en_US |
dc.subject | Expression | en_US |
dc.subject | Receptor | en_US |
dc.subject | Mellitus | en_US |
dc.subject | Release | en_US |
dc.subject | Glucose | en_US |
dc.subject | Men | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Amlodipine | en_US |
dc.subject.mesh | Calcium channel blockers | en_US |
dc.subject.mesh | Diabetes mellitus, type 2 | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Homeostasis | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Hypertension | en_US |
dc.subject.mesh | Insulin resistance | en_US |
dc.subject.mesh | Leptin | en_US |
dc.subject.mesh | Lipids | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Obesity | en_US |
dc.subject.mesh | Prospective studies | en_US |
dc.subject.mesh | Tumor necrosis factor-alpha | en_US |
dc.title | Effect of amlodipine on insulin resistance & tumor necrosis factor-alpha levels in hypertensive obese type 2 diabetic patients | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000225841600011 | tr_TR |
dc.identifier.scopus | 2-s2.0-11044234746 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0003-0463-6818 | tr_TR |
dc.identifier.startpage | 481 | tr_TR |
dc.identifier.endpage | 488 | tr_TR |
dc.identifier.volume | 120 | tr_TR |
dc.identifier.issue | 5 | tr_TR |
dc.relation.journal | Indian Journal of Medical Research | en_US |
dc.contributor.buuauthor | Ersoy, Canan | - |
dc.contributor.buuauthor | İmamoğlu, Şazi | - |
dc.contributor.buuauthor | Budak, Ferah | - |
dc.contributor.buuauthor | Tuncel, Ercan | - |
dc.contributor.buuauthor | Ertürk, Erdinç | - |
dc.contributor.buuauthor | Oral, Haluk Barbaros | - |
dc.contributor.researcherid | AAH-8861-2021 | tr_TR |
dc.contributor.researcherid | F-4657-2014 | tr_TR |
dc.contributor.researcherid | K-7285-2012 | tr_TR |
dc.identifier.pubmed | 15591634 | tr_TR |
dc.subject.wos | Immunology | en_US |
dc.subject.wos | Medicine, general and internal | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | Pubmed | en_US |
dc.wos.quartile | Q4 (Immunology) | en_US |
dc.wos.quartile | Q3 | en_US |
dc.contributor.scopusid | 6701485882 | tr_TR |
dc.contributor.scopusid | 6602297533 | tr_TR |
dc.contributor.scopusid | 6701913697 | tr_TR |
dc.contributor.scopusid | 7006929833 | tr_TR |
dc.contributor.scopusid | 7005488796 | tr_TR |
dc.contributor.scopusid | 7004498001 | tr_TR |
dc.subject.scopus | Telmisartan; Antihypertensive Agent; Hydrochlorothiazide Drug Combination Telmisartan | en_US |
dc.subject.emtree | Amlodipine | en_US |
dc.subject.emtree | Angiotensin 2 receptor antagonist | en_US |
dc.subject.emtree | Beta adrenergic receptor blocking agent | en_US |
dc.subject.emtree | Calcium channel blocking agent | en_US |
dc.subject.emtree | Dipeptidyl carboxypeptidase inhibitor | en_US |
dc.subject.emtree | Gliclazide | en_US |
dc.subject.emtree | Insulin | en_US |
dc.subject.emtree | Leptin | ten_US |
dc.subject.emtree | Long acting drug | en_US |
dc.subject.emtree | Monovas | en_US |
dc.subject.emtree | Thiazide diuretic agent | en_US |
dc.subject.emtree | Tumor necrosis factor alpha | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Aged | en_US |
dc.subject.emtree | Anthropometry | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Blood pressure | en_US |
dc.subject.emtree | Clinical trial | en_US |
dc.subject.emtree | Controlled clinical trial | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Correlation analysis | en_US |
dc.subject.emtree | Diastolic blood pressure | en_US |
dc.subject.emtree | Diet restriction | en_US |
dc.subject.emtree | Dose response | en_US |
dc.subject.emtree | Drug mechanism | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Glucose blood level | en_US |
dc.subject.emtree | Homeostasis | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Hypertension | en_US |
dc.subject.emtree | Insulin resistance | en_US |
dc.subject.emtree | Leg edema | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Metabolic parameters | en_US |
dc.subject.emtree | Non insulin dependent diabetes mellitus | en_US |
dc.subject.emtree | Obesity | en_US |
dc.subject.emtree | Systolic blood pressure | en_US |
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