LETTER TO THE EDITOR
Is the interaction between ticlopidine and cyclosporin dose related? Report of three cases
Published: 1 July 2010
Citation: Libyan J Med 2010, 5: 5334 - DOI: 10.3402/ljm.v5i0.5334
Libyan J Med 2010. © 2010 Tarik Sqalli Houssaïni et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/), permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Ticlopidine is an effective anti-platelet agent used for prevention of thrombosis (1–3). It was reported that treatment with ticlopidine at the dose of 250 mg daily in kidney transplant patients caused significant reduction of cyclosporin A (CsA) blood levels (4, 5). In heart transplant patients treated with higher doses of ticlopidine 500 mg daily, it was found to cause significant decrease of cyclosporin concentration but not in those treated with only 250 mg daily (1, 2). It was thought that ticlopidine interacts with cyclosporin metabolism at cytochrome P450 (1–3).
We report three living kidney donor recipients whose blood level of cyclosporin decreased significantly under treatment with a very low dose of ticlopidine of 100 mg daily.
The patients were on immunosuppressive treatment with steroids, CsA, and mycophenolate mofetil (MMF) or azathioprin. The total daily CsA dose was 125–150 mg. The patients developed severe hypertension 15 days to 4 months after kidney transplantation. Serum creatinine was normal except in patient number 2 (Table 1). Doppler ultrasonography confirmed significant stenosis of at least 70% degree in the artery of the transplanted kidney. Percutanuous transluminal angioplasty (PTA) with stent placement was performed. Anti-platelet treatment with aspirin (160 mg/day) and ticlopidine (100 mg/day) were given to prevent thrombosis. CsA blood levels were monitored by C0 (before morning dose) (Fig. 1). Under ticlopidine treatment, CsA blood levels decreased in patient 1 from 137 to 112 ng/ml, in patient 2 it decreased from 120 to 100 ng/ml, and in patient 3 it decreased from 131 to 106 ng/ml. Consequently CsA dose had been increased by 50–75 mg/day. No signs of acute kidney transplant rejection were observed.
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Fig. 1.
Cyclosporin A blood levels (C0) and doses during 60 days of ticlopidine therapy: follow of blood CsA levels and doses in the three patients.
In summary: In kidney transplant patients, ticlopidine can cause a significant decrease in CsA blood level even at a low dose of ticlopidine. The interaction of ticlopidine with CsA seems to be not related to the doses. We recommend careful monitoring of CsA blood level in patients treated with ticlopidine.
Tarik Sqalli Houssaïni
Nephrology department
Ibn Sina University Hospital
Rabat, Morocco
Email: tariksqalli@hotmail.com
Asmaâ Laboudi, Hakima Rhou, Fatima Ezzaïtouni
Loubna Benamar, Naïma Ouzeddoun, Rabea Bayahia
Nephrology department
Ibn Sina University Hospital
Rabat, Morocco
References
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- Campana C, Regazzi MB, Buggia I, Molinaro M. Clinically significant drug interactions with cyclosporin. An update. Clin Pharmacokinet. 1996; 30: 141–79. [Crossref]
- Feriozzi S, Massimetti C, Ancarani E. Treatment with ticlopidine is associated with reduction of cyclosporin A blood levels. Nephron. 2002; 92: 249–50. [Crossref]
- Verdejo A, De Cos MA, Zubimendi JA. Probable interaction between cyclosporin A and low dose ticlopidine. BMJ. 2000; 320: 1037. [Crossref]
Libyan Journal of Medicine eISSN 1819-6357, ISSN 1993-2820
This journal is published under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License. Responsible editor: Omran Bakoush