Research Article
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Lipoprotein aferezi homozigot ailevi hiperkolesterolemi hastalarında ventriküler repolarizasyonu etkiler

Year 2019, Volume: 10 Issue: 3, 340 - 347, 30.09.2019
https://doi.org/10.18663/tjcl.568661

Abstract

Amaç:
Homozigot ailevi hiperkolesterolemisi (HoAH)
olan hastalar erken yaşlarda kardiyovasküler hastalığa yakalanma riski altındadırlar
ve genellikle genç yaşta ani kardiyak ölüm (SCD) nedeniyle kaybedilirler. Bu
hastalarda ömrü uzatmak amacı ile tercih edilen tedavi yöntemi lipoprotein
aferezidir (LA). LA’nın kısa ve uzun dönem klinik faydalarından açıklamak için
çeşitli mekanizmalar önerilmiştir. Bu çalışmada, HoAH’si olan hastalarda tek
seans LA'nın, ventriküler repolarizasyon parametreleri üzerine olan etkisini
araştırdık.

Gereç ve Yöntemler:
LA uygulanan 11 HoAH hastası çalışmaya dahil edildi. Hastaların ortalama yaşı
30.1 ± 5,5 yıl ve hastaların %63,6’sı erkek idi. Tüm hastalara double
filtrasyon plazmaferez uygulandı.  İşlem
öncesi ve sonrasında hastaların ventriküler repolarizasyon parametrelerinden
OT, QTc aralığı, Tp-e aralığı, Tp-e / QT ve Tp-e / QTc oranı incelendi.

Bulgular:
Tek seans lipoprotein aferezi LDL'yi anlamlı bir şekilde düşürdü (10.04 ±
1.91'den 4.16 ± 1.21 mmol / L, P <001). İşlem sonrası plazma kalsiyum ve
magnezyum seviyeleri anlamlı derecede azaldı. QTc 443.8 ± 23.3 ms'den 412.3 ±
20.0 ms'ye (P <0.001) düştüğü saptandı. Tp-e aralığı ve Tp-e / QTc oranları
önemli ölçüde azaldı [85 (70-89) ms ile 63 (58-71) ms; P = 0.003 ve 0.19
(0.16-0.20) - 0.15 (0.13-0.16); P = 0,003, 
sırasıyla].







Sonuç:
Verilerimiz, tek bir lipoprotein aferez seansının bile elektrokardiyografik
repolarizasyon indekslerini iyileştirdiğini göstermiştir.

References

  • 1. Cuchel M, Bruckert E, Ginsberg HN et al. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society. European Heart Journal 2014; 35: 2146-57.
  • 2. Goldberg AC, Hopkins PN, Toth PP et al. Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia. Journal of Clinical Lipidology 2011; 5:133-40.
  • 3. Julius U, Frind A, Tselmin S, Kopprasch S, Poberschin I, Siegert G. Comparison of different LDL apheresis methods. Expert Review of Cardiovascular Therapy 2008; 6: 629-39.
  • 4. Thompsen J, Thompson PD. A systematic review of LDL apheresis in the treatment of cardiovascular disease. Atherosclerosis 2006; 189: 31-38.
  • 5. Kopprasch S, Graessler J, Bornstein SR et al. Beyond lowering circulating LDL: apheresis-induced changes of systemic oxidative stress markers by four different techniques. Atherosclerosis Supplements 2009; 10: 34-38.
  • 6. Kopprasch S, Julius U, Gromeier S, Kuhne H, Graessler J. Distinct effects of LDL apheresis by hemoperfusion (DALI) and heparin-induced extracorporeal precipitation (HELP) on leukocyte respiratory burst activity of patients with familial hypercholesterolemia. Journal of Clinical Apheresis 2000; 15: 249-55.
  • 7. Ramunni A, Burzo M, Verno L, Brescia P. Pleiotropic effects of LDL apheresis. Atherosclerosis Supplements 2009; 10: 53-55.
  • 8. Reimann M, Julius U, Haink K et al. LDL apheresis improves deranged cardiovagal modulation in hypercholesterolemic patients. Atherosclerosis 2010; 213: 212-17.
  • 9. Antzelevitch C. T peak-Tend interval as an index of transmural dispersion of repolarization. European Journal of Clinical Investigation. 2001; 31: 555-57.
  • 10. Antzelevitch C. Role of spatial dispersion of repolarization in inherited and acquired sudden cardiac death syndromes. American Journal of Physiology Heart and Circulatory 2007; 293: 2024-38
  • 11. Kroon AA, van't Hof MA, Demacker PN, Stalenhoef AF. The rebound of lipoproteins after LDL-apheresis. Kinetics and estimation of mean lipoprotein levels. Atherosclerosis. 2000; 152: 519-26.
  • 12. Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clinical Chemistry 1972; 18: 499-502.
  • 13. Yan GX, Antzelevitch C. Cellular basis for the normal T wave and the electrocardiographic manifestations of the long-QT syndrome. Circulation 1998; 98: 1928-36.
  • 14. Watanabe N, Kobayashi Y, Tanno K et al. Transmural dispersion of repolarization and ventricular tachyarrhythmias. Journal of Electrocardiology 2004; 37: 191-200.
  • 15. Wang Y, Lammi-Keefe CJ, Hou L, Hu G. Impact of low-density lipoprotein cholesterol on cardiovascular outcomes in people with type 2 diabetes: a meta-analysis of prospective cohort studies. Diabetes Research and Clinical Practice. 2013; 102: 65-75.
  • 16. Mabuchi H, Koizumi J, Shimizu M et al. Long-term efficacy of low-density lipoprotein apheresis on coronary heart disease in familial hypercholesterolemia. Hokuriku-FH-LDL-Apheresis Study Group. The American Journal of Cardiology. 1998; 82: 1489-95.
  • 17. Tamai O, Matsuoka H, Itabe H, Wada Y, Kohno K, Imaizumi T. Single LDL apheresis improves endothelium-dependent vasodilatation in hypercholesterolemic humans. Circulation 1997; 95: 76-82.
  • 18. Igarashi K, Tsuji M, Nishimura M, Horimoto M. Improvement of endothelium-dependent coronary vasodilation after a single LDL apheresis in patients with hypercholesterolemia. Journal of Clinical Apheresis 2004; 19: 11-16.
  • 19. Mellwig KP, Baller D, Gleichmann U et al. Improvement of coronary vasodilatation capacity through single LDL apheresis. Atherosclerosis. 1998; 139: 173-78.
  • 20. Chiu HC, Kovacs A, Blanton R et al. Transgenic expression of fatty acid transport protein 1 in the heart causes lipotoxic cardiomyopathy. Circulation Research. 2005; 96: 225-33.
  • 21. Park TS, Hu Y, Noh HL et al. Ceramide is a cardiotoxin in lipotoxic cardiomyopathy. Journal of Lipid Research 2008; 49: 2101-12.
  • 22. Lin LC, Wu CC, Yeh HI et al. Downregulated myocardial connexin 43 and suppressed contractility in rabbits subjected to a cholesterol-enriched diet. Lab Invest 2005; 85: 1224-37.
  • 23. Meenagh C, Mulholland C, Ryan MF. Magnesium homeostasis and antipsychotic-induced QTc prolongation. Journal of Psychopharmacology 2004; 18: 438-39.
  • 24. Vemuri R, Philipson KD. Influence of sterols and phospholipids on sarcolemmal and sarcoplasmic reticular cation transporters. The Journal of biological chemistry. 1989; 264: 8680-85.
  • 25. Ortega A, Mas-Oliva J. Cholesterol effect on enzyme activity of the sarcolemmal (Ca2+ + Mg2+)-ATPase from cardiac muscle. Biochimica et Biophysica Acta. 1984; 773: 231-36.
  • 26. Moffat MP, Dhalla NS. Heart sarcolemmal ATPase and calcium binding activities in rats fed a high cholesterol diet. The Canadian Journal of Cardiology. 1985; 1: 194-200.
  • 27. Chen CC, Lin YC, Chen SA et al. Shortening of cardiac action potentials in endotoxic shock in guinea pigs is caused by an increase in nitric oxide activity and activation of the adenosine triphosphate-sensitive potassium channel. Critical Care Medicine 2000; 28: 1713-20.
  • 28. Kulmatycki KM, Abouchehade K, Sattari S, Jamali F. Drug-disease interactions: reduced beta-adrenergic and potassium channel antagonist activities of sotalol in the presence of acute and chronic inflammatory conditions in the rat. British Journal of Pharmacology 2001; 133: 286-94.

Lipoprotein apheresis affects ventricular repolarization in patients with homozygous familial hypercholesterolemia

Year 2019, Volume: 10 Issue: 3, 340 - 347, 30.09.2019
https://doi.org/10.18663/tjcl.568661

Abstract

Aim:  Patients
with
Homozygous Familial
Hypercholesterolemia (HoFH)
prone to experience premature
cardiovascular disease and often die from sudden cardiac death (SCD) at a young
age.
Lipoprotein
apheresis (LA) is the treatment of choice to prolong survival. Several
mechanisms has been suggested to be responsible for the known short and
long-term clinical benefits of this procedure. This study was conducted to
assess the effect of single LA on ventricular repolarization parameters in
patients with HoFH.

Material and Methods: Eleven patients (mean
age 30.1 ± 5.5 years, male 63.6%)
with HoFH on chronic LA treatment were
enrolled in this preliminary study. Double filtration plasmapheresis (DFPP) was
performed in all patients.
To examine the effects of a single
session of LA, on ventricular repolarization,
the OT, QTc
interval, the T peak-to-end (Tp-e) interval, Tp-e/QT and the Tp-e/QTc ratio
were specifically calculated.

Results:
The single session of LA reduced total LDL (from 10.04 ± 1.91 to 4.16 ± 1.21
mmol/L, P<001).
The heart rate did
not change significantly after LA session.
Plasma levels of
calcium and magnesium was significantly decreased after the procedure. The QTc
decreased from
443.8 ± 23.3 ms to 412.3
± 20.0
ms (P <0.001). The Tp-e interval and the Tp-e/QTc ratio decreased significantly [85
(70-89)
ms vs. 63 (58-71)ms; P =0.003,
and
0.19
(0.16-0.20)
vs 0.15
(0.13-0.16);
P =0.003, respectively].







Conclusion: Our
data suggest that
even a
single session of LA improved electrocardiographic repolarization indexes.

References

  • 1. Cuchel M, Bruckert E, Ginsberg HN et al. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society. European Heart Journal 2014; 35: 2146-57.
  • 2. Goldberg AC, Hopkins PN, Toth PP et al. Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia. Journal of Clinical Lipidology 2011; 5:133-40.
  • 3. Julius U, Frind A, Tselmin S, Kopprasch S, Poberschin I, Siegert G. Comparison of different LDL apheresis methods. Expert Review of Cardiovascular Therapy 2008; 6: 629-39.
  • 4. Thompsen J, Thompson PD. A systematic review of LDL apheresis in the treatment of cardiovascular disease. Atherosclerosis 2006; 189: 31-38.
  • 5. Kopprasch S, Graessler J, Bornstein SR et al. Beyond lowering circulating LDL: apheresis-induced changes of systemic oxidative stress markers by four different techniques. Atherosclerosis Supplements 2009; 10: 34-38.
  • 6. Kopprasch S, Julius U, Gromeier S, Kuhne H, Graessler J. Distinct effects of LDL apheresis by hemoperfusion (DALI) and heparin-induced extracorporeal precipitation (HELP) on leukocyte respiratory burst activity of patients with familial hypercholesterolemia. Journal of Clinical Apheresis 2000; 15: 249-55.
  • 7. Ramunni A, Burzo M, Verno L, Brescia P. Pleiotropic effects of LDL apheresis. Atherosclerosis Supplements 2009; 10: 53-55.
  • 8. Reimann M, Julius U, Haink K et al. LDL apheresis improves deranged cardiovagal modulation in hypercholesterolemic patients. Atherosclerosis 2010; 213: 212-17.
  • 9. Antzelevitch C. T peak-Tend interval as an index of transmural dispersion of repolarization. European Journal of Clinical Investigation. 2001; 31: 555-57.
  • 10. Antzelevitch C. Role of spatial dispersion of repolarization in inherited and acquired sudden cardiac death syndromes. American Journal of Physiology Heart and Circulatory 2007; 293: 2024-38
  • 11. Kroon AA, van't Hof MA, Demacker PN, Stalenhoef AF. The rebound of lipoproteins after LDL-apheresis. Kinetics and estimation of mean lipoprotein levels. Atherosclerosis. 2000; 152: 519-26.
  • 12. Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clinical Chemistry 1972; 18: 499-502.
  • 13. Yan GX, Antzelevitch C. Cellular basis for the normal T wave and the electrocardiographic manifestations of the long-QT syndrome. Circulation 1998; 98: 1928-36.
  • 14. Watanabe N, Kobayashi Y, Tanno K et al. Transmural dispersion of repolarization and ventricular tachyarrhythmias. Journal of Electrocardiology 2004; 37: 191-200.
  • 15. Wang Y, Lammi-Keefe CJ, Hou L, Hu G. Impact of low-density lipoprotein cholesterol on cardiovascular outcomes in people with type 2 diabetes: a meta-analysis of prospective cohort studies. Diabetes Research and Clinical Practice. 2013; 102: 65-75.
  • 16. Mabuchi H, Koizumi J, Shimizu M et al. Long-term efficacy of low-density lipoprotein apheresis on coronary heart disease in familial hypercholesterolemia. Hokuriku-FH-LDL-Apheresis Study Group. The American Journal of Cardiology. 1998; 82: 1489-95.
  • 17. Tamai O, Matsuoka H, Itabe H, Wada Y, Kohno K, Imaizumi T. Single LDL apheresis improves endothelium-dependent vasodilatation in hypercholesterolemic humans. Circulation 1997; 95: 76-82.
  • 18. Igarashi K, Tsuji M, Nishimura M, Horimoto M. Improvement of endothelium-dependent coronary vasodilation after a single LDL apheresis in patients with hypercholesterolemia. Journal of Clinical Apheresis 2004; 19: 11-16.
  • 19. Mellwig KP, Baller D, Gleichmann U et al. Improvement of coronary vasodilatation capacity through single LDL apheresis. Atherosclerosis. 1998; 139: 173-78.
  • 20. Chiu HC, Kovacs A, Blanton R et al. Transgenic expression of fatty acid transport protein 1 in the heart causes lipotoxic cardiomyopathy. Circulation Research. 2005; 96: 225-33.
  • 21. Park TS, Hu Y, Noh HL et al. Ceramide is a cardiotoxin in lipotoxic cardiomyopathy. Journal of Lipid Research 2008; 49: 2101-12.
  • 22. Lin LC, Wu CC, Yeh HI et al. Downregulated myocardial connexin 43 and suppressed contractility in rabbits subjected to a cholesterol-enriched diet. Lab Invest 2005; 85: 1224-37.
  • 23. Meenagh C, Mulholland C, Ryan MF. Magnesium homeostasis and antipsychotic-induced QTc prolongation. Journal of Psychopharmacology 2004; 18: 438-39.
  • 24. Vemuri R, Philipson KD. Influence of sterols and phospholipids on sarcolemmal and sarcoplasmic reticular cation transporters. The Journal of biological chemistry. 1989; 264: 8680-85.
  • 25. Ortega A, Mas-Oliva J. Cholesterol effect on enzyme activity of the sarcolemmal (Ca2+ + Mg2+)-ATPase from cardiac muscle. Biochimica et Biophysica Acta. 1984; 773: 231-36.
  • 26. Moffat MP, Dhalla NS. Heart sarcolemmal ATPase and calcium binding activities in rats fed a high cholesterol diet. The Canadian Journal of Cardiology. 1985; 1: 194-200.
  • 27. Chen CC, Lin YC, Chen SA et al. Shortening of cardiac action potentials in endotoxic shock in guinea pigs is caused by an increase in nitric oxide activity and activation of the adenosine triphosphate-sensitive potassium channel. Critical Care Medicine 2000; 28: 1713-20.
  • 28. Kulmatycki KM, Abouchehade K, Sattari S, Jamali F. Drug-disease interactions: reduced beta-adrenergic and potassium channel antagonist activities of sotalol in the presence of acute and chronic inflammatory conditions in the rat. British Journal of Pharmacology 2001; 133: 286-94.
There are 28 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Orıgınal Artıcle
Authors

Firdevs Ayşenur Ekizler 0000-0002-3988-6828

Serkan Cay 0000-0002-5476-1214

Burak Acar 0000-0003-3217-5000

Bahar Tekin Tak This is me 0000-0003-0971-597X

Elif Hande Ozcan Cetin 0000-0001-5969-2345

Ahmet Temizhan

Publication Date September 30, 2019
Published in Issue Year 2019 Volume: 10 Issue: 3

Cite

APA Ekizler, F. A., Cay, S., Acar, B., Tak, B. T., et al. (2019). Lipoprotein apheresis affects ventricular repolarization in patients with homozygous familial hypercholesterolemia. Turkish Journal of Clinics and Laboratory, 10(3), 340-347. https://doi.org/10.18663/tjcl.568661
AMA Ekizler FA, Cay S, Acar B, Tak BT, Cetin EHO, Temizhan A. Lipoprotein apheresis affects ventricular repolarization in patients with homozygous familial hypercholesterolemia. TJCL. September 2019;10(3):340-347. doi:10.18663/tjcl.568661
Chicago Ekizler, Firdevs Ayşenur, Serkan Cay, Burak Acar, Bahar Tekin Tak, Elif Hande Ozcan Cetin, and Ahmet Temizhan. “Lipoprotein Apheresis Affects Ventricular Repolarization in Patients With Homozygous Familial Hypercholesterolemia”. Turkish Journal of Clinics and Laboratory 10, no. 3 (September 2019): 340-47. https://doi.org/10.18663/tjcl.568661.
EndNote Ekizler FA, Cay S, Acar B, Tak BT, Cetin EHO, Temizhan A (September 1, 2019) Lipoprotein apheresis affects ventricular repolarization in patients with homozygous familial hypercholesterolemia. Turkish Journal of Clinics and Laboratory 10 3 340–347.
IEEE F. A. Ekizler, S. Cay, B. Acar, B. T. Tak, E. H. O. Cetin, and A. Temizhan, “Lipoprotein apheresis affects ventricular repolarization in patients with homozygous familial hypercholesterolemia”, TJCL, vol. 10, no. 3, pp. 340–347, 2019, doi: 10.18663/tjcl.568661.
ISNAD Ekizler, Firdevs Ayşenur et al. “Lipoprotein Apheresis Affects Ventricular Repolarization in Patients With Homozygous Familial Hypercholesterolemia”. Turkish Journal of Clinics and Laboratory 10/3 (September 2019), 340-347. https://doi.org/10.18663/tjcl.568661.
JAMA Ekizler FA, Cay S, Acar B, Tak BT, Cetin EHO, Temizhan A. Lipoprotein apheresis affects ventricular repolarization in patients with homozygous familial hypercholesterolemia. TJCL. 2019;10:340–347.
MLA Ekizler, Firdevs Ayşenur et al. “Lipoprotein Apheresis Affects Ventricular Repolarization in Patients With Homozygous Familial Hypercholesterolemia”. Turkish Journal of Clinics and Laboratory, vol. 10, no. 3, 2019, pp. 340-7, doi:10.18663/tjcl.568661.
Vancouver Ekizler FA, Cay S, Acar B, Tak BT, Cetin EHO, Temizhan A. Lipoprotein apheresis affects ventricular repolarization in patients with homozygous familial hypercholesterolemia. TJCL. 2019;10(3):340-7.


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