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001-es BibID:BIBFORM071387
Első szerző:Harangi Mariann (belgyógyász, endokrinológus)
Cím:HDL subfraction distribution and HDL function in untreated dyslipidemic patients / Harangi Mariann, Szentpéteri Anita, Nádró Bíborka, Lőrincz Hajnalka, Seres Ildikó, Páll Dénes, Paragh György
Dátum:2017
ISSN:2574-1209
Megjegyzések:Aim: The protective role of high-density lipoprotein (HDL) against atherosclerosis is wellknown. However, both structural and functional changes of the HDL particles may affect itsprotective efficacy. Increased levels of HDL-associated myeloperoxidase (MPO) and decreasedHDL-linked paraoxonase-1 (PON1) activity have been reported in dyslipidemic patients. Somechanges in HDL subfraction distributions were also studied previously, but data on structuraland functional changes in dyslipidemia are not complete. Therefore, the authors aimed toevaluate these qualitative and quantitative markers of HDL in dyslipidemic patients andhealthy control subjects. Methods: Anthropometric parameters, serum levels of lipoproteinsand MPO, as well as PON1 activities were investigated in 81 untreated dyslipidemic patientsand in 32 healthy gender-matched controls. Additionally, HDL subfractions were detectedby an electrophoretic method on polyacrylamide gel (Lipoprint). Results: Significantlyhigher glucose, hemoglobin A1c, total cholesterol, low-density lipoprotein-cholesterol,triglyceride, lipoprotein(a), apolipoprotein B, C-reactive protein, and MPO levels were foundin patients compared to the healthy subjects. There were no significant differences in PON1paraoxonase and arylesterase activities between the two study groups, but MPO/PON1 ratiowas significantly higher in patients. There was a shift towards the smaller HDL subfractions,but only the intermediate HDL ratio was significantly lower in patients compared to controls.Conclusion: The results highlight the importance of HDL-associated pro- and antioxidantenzymes suggesting the possible clinical benefit of MPO/PON1 calculation and confirm thatquantification of HDL-C level alone provides limited data regarding HDL's cardioprotectiveeffect. Calculation of MPO/PON1 ratio may be a useful cardiovascular marker in dyslipidemia.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
subfraction
paraoxonase
myeloperoxidase
dyslipidemia
high-density lipoprotein
Megjelenés:Vessel Plus. - 1 (2017), p. 166-173. -
További szerzők:Szentpéteri Anita (1988-) (biológus) Nádró Bíborka (1992-) (általános orvos) Lőrincz Hajnalka (1986-) (biológus) Seres Ildikó (1954-) (biokémikus) Páll Dénes (1967-) (belgyógyász, kardiológus) Paragh György (1953-) (belgyógyász)
Pályázati támogatás:GINOP-2.3.2-15-2016-00062
GINOP
OTKA-115723
OTKA
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2.

001-es BibID:BIBFORM069720
Első szerző:Harangi Mariann (belgyógyász, endokrinológus)
Cím:LDL apheresis or PCSK9 inhibition? Sometimes we have to combine them / Mariann Harangi, Lilla Juhász, Bíborka Nádró, József Balla, György Paragh
Dátum:2017
Megjegyzések:This study presents the case of a female patient with severe heterozygous familialhypercholesterolemia. Despite the combined maximum dose oral treatment with rosuvastatinand ezetimibe, we found markedly elevated lipid parameters. Therefore, we indicated monthlyselective low density lipoprotein (LDL) apheresis treatment using the Direct Adsorption ofLipoproteins system. After more than 2 years the lipid levels of the patients were still above thetherapeutic goals. Finally, we completed the treatment by the inhibitor evolocumab biweekly.Further LDL cholesterol (LDL-C) reduction was achieved resulting in lipid parameters ongoals. However, administration of evolocumab without LDL apheresis could not reduce theLDL-C below 2.5 mmol/L. We concluded that both LDL apheresis and proprotein convertasesubtilisin/kexin type 9 (PCSK9) inhibitor treatments were effective and well tolerated. None ofthem alone would be enough to achieve lipid goals in this patient. However, the combination ofthese potent treatments may normalize the lipid levels and prevent cardiovascular complications.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
LDL apheresis
PCSK9 inhibition
familial hypercholesterolemia
low-density lipoprotein
lipoprotein(a)
Megjelenés:Vessel Plus. - 1 (2017), p. 91-95. -
További szerzők:Juhász Lilla (1990-) (általános orvos) Nádró Bíborka (1992-) (általános orvos) Balla József (1959-) (belgyógyász, nephrológus) Paragh György (1953-) (belgyógyász)
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Intézményi repozitóriumban (DEA) tárolt változat
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3.

001-es BibID:BIBFORM077799
Első szerző:Zsíros Noémi (belgyógyász)
Cím:Successful plasmapheresis treatment of severe hypertriglyceridemia during late pregnancy / Noémi Zsíros, Beáta Kovács, György Paragh, József Balla, Mariann Harangi
Dátum:2019
Megjegyzések:During pregnancy, physiologic hormonal changes provoke a significant increase in triglyceride levels. Genetic abnormalities of triglyceride metabolism and secondary factors may multiply the risk of severe lipid abnormalities. Although severe gestational hypertriglyceridemia can be a life-threatening condition for both mother and fetus, its optimal treatment has not been fully clarified. A 33-year-old woman at 37 weeks of her second pregnancy was admitted to our clinic. Her triglyceride level was 57.8 mmol/L. Abdominal pain, nausea, vomiting or any other complaints were not reported. She kept a fat-restricted diet, however her triglyceride level remained 41 mmol/L. Therefore we decided to perform plasmapheresis with a replacement of human albumin as a colloidal solution. Complications did not occur during the treatment. Plasmapheresis reduced her triglyceride level by 54.1% (to 18.8 mmol/L), and the patient delivered a healthy female neonate at 40 weeks. In case of significantly increased values, plasmapheresis is a fast, effective and safe method for decreasing triglyceride level even in the third trimester.
Tárgyszavak:Orvostudományok Klinikai orvostudományok esettanulmány
folyóiratcikk
Hypertriglyceridemia
pregnancy
plasmapheresis
Megjelenés:Vessel Plus. - 3 : 6 (2019), p. 1-6. -
További szerzők:Kovács Beáta (1989-) (belgyógyász) Paragh György (1953-) (belgyógyász) Balla József (1959-) (belgyógyász, nephrológus) Harangi Mariann (1974-) (belgyógyász, endokrinológus)
Pályázati támogatás:GINOP-2.3.2-15-2016-00005
GINOP
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Intézményi repozitóriumban (DEA) tárolt változat
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