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      Influence of lipid metabolism disorders on venous thrombosis risk Translated title: Uticaj poremećaja lipidnog metabolizma na rizik od venske tromboze

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          Abstract

          Background: To investigate the influence of lipid metabolism disorders on the risk of deep vein thrombosis.

          Methods: A total of 200 subjects participated in the study, 100 of whom experienced DVT with or without PTE, and 100 healthy subjects representing the control group. We classified patients and controls in terms of serum concentrations of chylomicrons, LDL, IDL, VLDL, and HDL particles, as those with or without hyperlipoproteinemia and in terms of serum Lp (a) lipoprotein levels, as those with hyperLp (a) lipoproteinemia (serum Lp (a) values >0.3 g/L) and those without hyperLp (a) lipoproteinemia (serum Lp (a) values <0.3 g/L). Based on the modified and supplemented Fredrickson classification, participants with verified existences of hyperlipoproteinemia were classified into subgroups based on the type of hyperlipoproteinemia. Unconditional logistic regression was used to calculate ORs with 95% CIS as a measure of the relative risks for venous thrombosis in participants with hyperlipoproteinemia compared with those without hyperlipoproteinemia. The analysis was adjusted for all potential confounders (age, sex, obesity) related to the functionality of the lipid metabolism, and at the same time, may have an impact on the risk of venous thrombosis.

          Results: The results of the comparison of the mean values of individual lipid status parameters between the patient group and the control group clearly indicate higher concentrations of total cholesterol (5.93 mmol/L vs. 5.52 mmol/L), total triglycerides (1.58 mmol/L vs. 1.50 mmol/L), and LDL-cholesterol (3.83 mmol/L vs. 3.44 mmol/L) in the patient group relative to the control group, with a statistically significant difference observed only in the case of LDL-cholesterol concentrations. We have found that type IIa hyperlipoproteinemia is associated with a nearly double increased risk for deep vein thrombosis (OR 1.99; Cl 1.01-3.90), while type IIb, IV, or hyperLp (a) lipoproteinemia did not influence the risk (OR 1.22; 95% Cl 0.79-1.84; OR 0.89; 95% Cl 0.52-1.54 OR 1.85; 95% CI 0.84-4.04).

          Conclusions: Hypercholesterolemia doubles the risk of deep vein thrombosis development.

          Translated abstract

          Uvod: Cilj je bio da se istraži uticaj poremećaja metabolizma lipida na rizik od razvoja tromboze dubokih vena.

          Metode: U istraživanju je učestvovalo ukupno 200 ispitanika, od kojih je 100 doživelo DVT sa ili bez PTE i 100 zdravih ispitanika koji su predstavljali kontrolnu grupu. Pacijente i kontrolnu grupu klasifikovali smo prema serumskim koncentracijama hilomikrona, LDL, IDL, VLDL i HDL čestica, na one sa ili bez hiperlipoproteinemije i prema nivou Lp (a) lipoproteina u serumu, na one sa hiperLp (a) lipoproteinemijom (serumske vrednosti Lp (a) > 0,3 g/L) i one bez hiperLp (a) lipoproteinemije (vrednosti Lp (a) u serumu < 0,3 g/L). Na osnovu modifikovane i dopunjene Fredriksonove klasifikacije ispitanici sa dokazanim postojanjem hiperlipoproteinemije razvrstani su u podgrupe prema tipu hiperlipoproteinemije. Ne kondicionalna logistička regresija je korištena za izračunavanje OR-a sa 95% CI kao mere relativnog rizika od venske tromboze kod ispitanika sa hiperlipoproteinemijom u poređenju sa onima bez hiperlipoproteinemije. Analiza je prilagođena za sve potencijalne "confoundere" (uzrast, pol, gojaznost) koji se odnose na funkcionalnost metabolizma lipida, a istovremeno mogu imati uticaj na rizik od nastanka venske tromboze.

          Rezultati: Rezultati poređenja srednjih vrednosti pojedinačnih parametara lipidnog statusa između grupe pacijenata i kontrolne grupe jasno ukazuju na veće koncentracije ukupnog holesterola (5,93 mmol/L naspram 5,52 mmol/L), ukupnih triglicerida (1,58 mmol/L naspram 1,50 mmol/L) i LDL-holesterola (3,83 mmol/L naspram 3,44 mmol/L) u grupi pacijenata u odnosu na kontrolnu grupu, sa statistički značajnom razlikom uočenom samo u slučaju koncentracije LDL-holesterola. Otkriveno je da je hiperlipoproteinemija tipa IIa povezana sa gotovo dvostruko većim rizikom od duboke venske tromboze (OR 1,99; Cl 1,01-3, 90), dok lipoproteinemija tipa IIb, IV ili hyperLp (a) nije uticala na rizik (OR 1,22; 95% Cl 0,79-1,84; OR 0,89; 95% Cl 0,52-1,54 ILI 1,85; 95% CI 0,84-4,04).

          Zaključak: Hiperholesterolemija udvostručuje rizik od razvoja tromboze dubokih vena.

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          Incidence and mortality of venous thrombosis: a population-based study.

          Estimates of the incidence of venous thrombosis (VT) vary, and data on mortality are limited. We estimated the incidence and mortality of a first VT event in a general population. From the residents of Nord-Trøndelag county in Norway aged 20 years and older (n = 94 194), we identified all cases with an objectively verified diagnosis of VT that occurred between 1995 and 2001. Patients and diagnosis characteristics were retrieved from medical records. Seven hundred and forty patients were identified with a first diagnosis of VT during 516,405 person-years of follow-up. The incidence rate for all first VT events was 1.43 per 1000 person-years [95% confidence interval (CI): 1.33-1.54], that for deep-vein thrombosis (DVT) was 0.93 per 1000 person-years (95% CI: 0.85-1.02), and that for pulmonary embolism (PE) was 0.50 per 1000 person-years (95% CI: 0.44-0.56). The incidence rates increased exponentially with age, and were slightly higher in women than in men. The 30-day case-fatality rate was higher in patients with PE than in those with DVT [9.7% vs. 4.6%, risk ratio 2.1 (95% CI: 1.2-3.7)]; it was also higher in patients with cancer than in patients without cancer [19.1% vs. 3.6%, risk ratio 3.8 (95% CI 1.6-9.2)]. The risk of dying was highest in the first months subsequent to the VT, after which it gradually approached the mortality rate in the general population. This study provides estimates of incidence and mortality of a first VT event in the general population.
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            Venous thromboembolism (VTE) in Europe. The number of VTE events and associated morbidity and mortality.

            Venous thromboembolism (VTE) is often asymptomatic, mis-diagnosed, and unrecognized at death, and there is a lack of routine postmortem examinations. These factors are thought to result in marked underestimates ofVTE incidence. The objective of our study was to estimate the total burden of VTE within the European Union (EU) per annum. An epidemiological model was constructed to estimate the number of community- and hospital-acquired incidents and recurrent cases (attack rate) of nonfatal VTE and VTE-related deaths, as well as incident and prevalent cases of post-thrombotic syndrome (PTS) and chronic thromboembolic pulmonary hypertension (PH) occurring in the EU per annum. Individual models were developed for six EU countries. The models were populated with data from published literature and, where necessary, expert opinions. The findings were tested using probabilistic sensitivity analyses. The estimated total number of symptomaticVTE events (range based on probabilistic sensitivity analysis) per annum within the six EU countries was 465,715 (404,664-538,189) cases of deep-vein thrombosis, 295,982 (242,450-360,363) cases of pulmonary embolism (PE), and 370,012 (300,193-483,108) VTE-related deaths. Of these deaths, an estimated 27,473 (7%) were diagnosed as being antemortem; 126,145 (34%) were sudden fatal PE, and 217,394 (59%) followed undiagnosed PE. Almost three-quarters of all VTE-related deaths were from hospital-acquired VTE. VTE is a major health problem in the EU, with over one million VTE events or deaths per annum in the six countries examined. Given the availability of effective VTE prophylaxis, many of these events and deaths could have been prevented. These results have important implications for the allocation of healthcare resources.
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              Venous thrombosis: a multicausal disease.

              The risk factors for venous thrombosis differ from those for arterial vascular disease. During the past 5 years, knowledge about the aetiology of venous thrombosis has advanced with the discovery of several factors that contribute to the incidence of thrombosis, particularly the role of coagulation abnormalities. These abnormalities are common in the general population and therefore will be present simultaneously in some individuals. The resultant gene-gene and gene-environment interactions between risk factors are the key to the understanding of why a certain person develops thrombosis at a specific point in time.
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                Author and article information

                Contributors
                Journal
                J Med Biochem
                J Med Biochem
                JOMB
                Journal of Medical Biochemistry
                Society of Medical Biochemists of Serbia, Belgrade
                1452-8258
                1452-8266
                05 June 2021
                05 June 2021
                05 June 2021
                : 40
                : 3
                : 245-251 (pp. 245-251)
                Affiliations
                [1 ] orgnameUniversity of Novi Sad, Faculty of Medicine, Department of Pathophysiology, Novi Sad
                [2 ] orgnameInstitute of Laboratory Diagnostics Medlab, Novi Sad
                [3 ] orgnameUniversity Business Academy, Faculty of Pharmacy Novi Sad, Novi Sad
                [4 ] orgnameClinical Center of Serbia, Belgrade
                Author notes

                Correspondence to: Igor Spasic, Department of Laboratory Diagnostics Medlab, 21/15, Branimira Cosica Street, 21000 Novi Sad, Vojvodina, Serbia igsp92@ 123456gmail.com

                Article
                jomb-40-3-2103245S
                10.5937/jomb0-27106
                8199415
                34177368
                da7fd74d-e2ed-47be-9911-ffc916771339
                2021 Igor Spasić, Milan Ubavić, Zorica Šumarac, Maša Todorović, Biljana Vučković, published by CEON/CEES

                This work is licensed under the Creative Commons Attribution 4.0 License.

                History
                : 20 September 2020
                : 16 June 2020
                Categories
                Original Paper

                dvt,hemostasis,hyperlioproteinemia,lipidmetabolism,lp (a) hyperlipoproteinemia,hemostaza,hiperlipoptroteinemija,metabolizam lipida,lp(a) hiperlipoproteinemija

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