4 research outputs found
Insulinska rezistencija, sistemska inflamacija i aterogeni faktori rizika kod bolesnika sa koronarnom boleÅ”Äu i razliÄitim hiperglikemijskim statusom
Uvod. Nedijagnostikovana hiperglikemija je Äesta kod bolesnika sa koronarnomboleÅ”Äu, koja je vodeÄi uzrok smrtnosti kod oboljelih od tipa 2 dijabetesa(T2DM). Nedovoljno je poznata povezanost blažih hiperglikemijskih stanja,kao Å”to je predijabetes sa koronarnom boleÅ”Äu. Cilj ove studije bio je uporeditikardiometaboliÄki profil rizika i koronarne lezije kod bolesnika sa razliÄitimporemeÄajima tolerancije na glukozu podvrgnutih koronarnoj angiografiji.Metode. Kod 106 bolesnika sa angiografski dijagnostikovanom koronarnomboleÅ”Äu, evaluiran je glikemijski status pomoÄu testa oralnog optereÄenja glukozom(OGTT) na osnovu kojeg su klasifikovani u grupe sa normoglikemijom(NGT), predijabetesom (IGF/IGT) i dijabetesom tipa 2 (T2DM). Kod svih jeuraÄeno mjerenje tjelesne težine (TT), obima struka (OS), izraÄunat indekstjelesne mase (BMI), odreÄeni lipidi, indeks insulinske rezistencije HOMA,insulin, hsCRP, albumin u urinu, broj signifikantnih koronarnih lezija (stenoza> 50%).Rezultati. Od 106 ispitanih bolesnika sa koronarnom boleÅ”Äu 32,1% imaloje novootkriveni T2DM, 35,8% predijabetes i 32,1% normalnu tolerancijuglukoze. Nije bilo razlika izmeÄu tri grupe koronarnih bolesnika u odnosuna pol, puÅ”aÄki status, tjelesnu masu, prisustvo hipertenzije i hereditet koronarnebolesti. Pacijenti sa T2DM u odnosu na pacijente sa normoglikemijomsu bili stariji (p = 0,036), imali veÄi obim struka (p = 0,028), BMI (p = 0,045) iHOMA-IR (p = 0,001). Vrijednosti ukupnog holesterola, LDL, HDL i triglicerida,hsCRP, albuminurije se nisu razlikovale izmeÄu grupa. Nije naÄenarazlika u uÄestalosti jednosudovne, dvosudovne, tro i viÅ”e sudovne bolesti.ZakljuÄak. NaÄena je visoka uÄestalost dijabetesa i predijabetesa u populacijipacijenata sa stabilnom hroniÄnom koronarnom boleÅ”Äu. NaÄena je povezanostgojaznosti, naroÄito centralne, starosti i insulinske rezistencije sa T2DM, Å”topotvrÄuje ulogu ovih faktora u nastanku bolesti
Albuminurija i intima-media kompleks karotidnih arterija kao surogat markeri ateroskleroze kod pacijenata sa tipom 2 dijabetesa
Uvod. KliniÄko procjenjivanje aterosklerotskih komplikacija u tipu 2 dijabetesmelitusa (DM) je preusmjereno na otkrivanje subkliniÄkih oblika aterosklerozeprimjenom neinvazivnih dijagnostiÄkih metoda. Surogat markeri subkliniÄkeateroskleroze su intima media kompleks (IMK) karotidnih arterija i albuminurija.Cilj rada je bio da se analizira povezanost prisustva albuminurije idebljine IMK karotidnih arterija sa nijemom ishemijom miokarda kod pacijenatasa tipom 2 DM.Metode. Istraživanje je obuhvatilo 62 ispitanika oboljela od tipa 2 dijabetesabez istorije o prisutnosti kardiovaskularnih bolesti (KVB), starosne dobi 40-70godina. Ispitanicima je uraÄena ergometrija i na osnovu dobijenih rezultatao prisutnosti ishemijske bolesti srca (IBS) podijeljeni su u dvije grupe. Prvugrupu je saÄinjavalo 25 ispitanika kojima je dokazana IBS, a drugu grupu37 ispitanika bez IBS. Ispitanicima je ultrazvuÄno izmjerena debljina IMKkarotidnih arterija i odreÄen albumin u 24-Äasovnom urinu, te su dobijenevrijednosti uporeÄene sa rezultatima ergometrijskog testiranja u obje grupe.Rezultati. Pacijenti sa IBS su bili stariji, sa dužim trajanjem dijabetesa, dislipidemijomi viÅ”im vrijednostima HbA1c u odnosu na grupu bez IBS (p<0,05).UtvrÄena je statistiÄki znaÄajno veÄa vrijednost debljine IMK karotidniharterija u grupi ispitanika sa IBS (1,08Ā±0,17 mm) u odnosu na ispitanike bezIBS (0,78Ā±0,17 mm) (p<0,001). U grupi ispitanika sa IBS, albuminurija je bilaprisutna kod 22 ispitanika, dok je kod ispitanika bez IBS, albuminurija bilaprisutna kod 9 ispitanika, Å”to je statistiÄki znaÄajno viÅ”e u grupi ispitanika saIBS u odnosu na kontrolnu grupu (p<0,001).ZakljuÄak. Pacijenti sa poveÄanom debljinom IMK karotidnih arterija i prisutnomalbuminurijom imaju veÄi rizik od nastanka IBS.KljuÄne rijeÄi: dijabetes melitus, intima media kompleks, albuminurij
Inflammatory cardiovascular risk markers and silent myocardial ischemia in type 2 diabetic patients
Background/Aim. A special feature of coronary heart disease (CHD) in patients with type 2 diabetes mellitus (T2DM) is that it is often a symptomatic and occurs as a consequence of cardiovascular autonomic neuropathy. Dysregulation of the autonomic nervous system is associated with elevated values of inflammatory markers such as high-sensitivity C-reactive protein (hs-CRP) and interleukin- 6 (IL-6), which accelerate atherosclerosis and the occurrence of cardiovascular complications in patients with T2DM. The aim of the study was to evaluate the importance of determining inflammatory cardiovascular risk markers IL-6 and hs-CRP in screening for the presence of CHD in asymptomatic patients with T2DM. Methods. The study included 169 patients with T2DM without any symptoms and signs of CHD. Ergometric testing proved or ruled out the presence of silent CHD. The levels of hs- CRP and IL-6 were determined by ELISA. Results. IL-6 values were significantly higher in patients with a positive ergometric test (6.83 Ā± 1.99 pg/mL) compared to patients with a negative ergometric test (3.04 Ā± 1.39 pg/mL) (p < 0.001). We also found that hs-CRP values in patients with a positive ergometric test were significantly higher compared to patients with a negative ergometric test (6.37 Ā± 2.25 vs 1.67 Ā± 1.41 mg/L; p < 0.001). Combinations of IL-6 and hs-CRP with age, HbA1c values, and duration of diabetes, presented through three binary logistic regression models, are significant predictors of silent CHD proven by ergometric testing, ie, with their increase, the probability of a positive ergometric test also increases (p < 0.01). The sensitivity of the associated finding of elevated IL-6 and hs-CRP values in the detection of silent CHD by ergometric testing was 90%, and the specificity was 86%. Conclusion. Hs-CRP and IL-6 are significant predictors of silent CHD, and their determination could be recommended for improving cardiovascular risk stratification in asymptomatic patients with T2DM
The Effect of Three-Month Vitamin D Supplementation on the Levels of Homocysteine Metabolism Markers and Inflammatory Cytokines in Sera of Psoriatic Patients
Psoriasis is an autoimmune and inflammatory skin disease. Psoriatic patients express higher levels of plasma homocysteine (Hcy) concentration and pro-inflammatory mediators than healthy people; this is frequently associated with vitamin D deficiency. The aim of this clinical study was to investigate the effects of high doses of vitamin D supplementation on the parameters of Hcy metabolism and cytokines in sera of psoriatic patients. This prospective study was conducted on 40 psoriatic patients who had the vitamin D deficiency. All patients received vitamin D 5000 IU/day for three months. Clinical and biochemical measurements were taken at baseline and at follow up (3 months). The results showed that the severity of clinical features, measured by the psoriasis area severity index (PASI) score, were considerably improved in patients after vitamin D supplementation. After vitamin D supplementation, most of the patients (n = 25 or 62.5%) had mild clinical form (p 12 serum levels in comparison to the levels that had been measured at the beginning of the study (56.77 Ā± 14.66 nmol/L and 301.08 Ā± 95.02 pg/mL vs. 103.85 Ā± 32.20 nmol/L and 362.81 Ā± 118.56 pg/mL, respectively; p < 0.001). Moreover, serum levels of Hcy and folate were significantly lower at the end of the study in comparison with the initial levels (12.45 Ā± 1.92 Āµmol/L and 8.01 Ā± 3.88 mg/mL vs. 10.38 Ā± 1.66 Āµmol/L and 6.27 Ā± 2.60 mg/mL, respectively). High doses of vitamin D supplementation led to a significant decrease in pro-inflammatory cytokines (IFN-ɤ, TNF-Ī±, IL-1Ī², IL-6, IL-8, and IL-17) and high-sensitivity C-reactive protein (hsCRP), whereas the production of anti-inflammatory cytokines (IL-10, IL-5) was up-regulated. In conclusion, supplementation with high doses of vitamin D could be one of the possible preventive and therapeutic measures to reduce systemic inflammation in psoriatic patients