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PRİMER MEMBRANOPROLİFERATİF GLOMERULONEFRİT TEDAVİSİNDE MİKOFENOLAT MOFETİL KULLANIMI: RETROSPEKTİF DEĞERLENDİRME

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Abstract (2. Language): 
Mycophenolate mofetil treatment of primary membranoproliferative glomevulonephritis: ret-rospective analysis. Primary membranoproliferative glomerulonephritis (MPGN) is a progres¬sive disease of which permanent remission rate is very low. In adult patients, its treatment consists of mainly Standard steroid drugs alone or combined with cytostatic drugs or other im-munosuppressive drugs like Cyclosporine-A. Mycophenolate Mofetil(MMF) is a new potenti-al drug in the treatment of primary glomerulonephritis. In our study 6 patients suffering from MPGN (3 vvomen, 3 men) that used MMF were analysed retrospectively; mean age was 31.6(18-50) years, the time of disease before MMF treatment was 17.8(2-70) months. Mycophenolate Mofetil dosages were lg (twice a day) in 4 patients, 0.75g(twice a day) in one patient and 0.5g (tvvice a day) in one patient in whom diabetes mellitus developed under steroid treatment. Mean MMF treatment duration was 8.08(6.5-10) months. Complete remission was achi-ved in 5 patients (the earliest at the first month, the latest in the 9.th month of MMF treatment). In one patient who is at the 6.th month of MMF treatment partial remission was provi-ded. This successfull rate of treatment may be attributed to the inhibitory effects of MMF on lymphocytes but also to antiproliferative efffects of MMF on glomerular mesangial cells and myofibroblasts. Beginning of the improvement in proteinuria, serum albumin and cholesterol levels were seen in the first month of the treatment an continued in the follovving months. No significant changes in serum creatinine levels were seen in the treatment time and no adverse effects of MMF was recorded. As a result, according to present study, MMF therapy alone or together with steroids to patients with MPGN vvhose renal functions are normal, seems to be beneficial.
Abstract (Original Language): 
Primer membranoproliferatif glomerulonefrit (MPGN) progressif seyirli ve kalıcı remisyon oranı düşük olan bir glomerulonefrittir, erişkinlerde konservatif tedaviye ek olarak standart steroid tedavisi ve birlikte sitotoksik veya siklosporin-A (CsA) gibi diğer immunosupressifler verilebilir. Bu tedavi uygulamalarına rağmen prognozu üzerinde belirgin iyileşmeler sağlanamamıştır. Mikofenolat mofetil (MMF); idiopatik glomeruler hastalıkların tedavisinde potansiyel yeni bir ilaçtır. Bu çalışmada MMF kullanılmış primer MPGN'li hastalarımız retrospektif olarak değerlendirilmiştir. Çalışmaya 3'ü erkek, 3'ü kadın olmak üzere toplam 6 hasta alınmıştır. Hastaların yaş ortalamaları 31.6(18-50) olup, MMF başlanmadan önceki MPGN tanı süresi ortalama 17.8 (2-70)ay idi. Hastaların dördüne 2xlg MMF başlanırken bir hastaya 2x0.75g/gün, diyabet gelişen bir hastaya ise 2x0.5g/giin dozunda MMF başlandı. Ortalama 8.08 (6.5-10) ay MMF tedavisi verilen hastalardan 5'inde (en erken 1., en geç 9. ayda, ortalama 5. ayda olmak üzere) tam remisyon saptanırken MMF tedavisinin 6.5 ayında olan bir hastada parsiyel remisyon sağlanmıştır. Hastaların MMF'ye bu kadar müspet yanıt vermesindeki ana mekanizmanın MMF'nin lenfositler üzerindeki immunosupressif etkileri yanında mezangi-yal hücre proliferasyonunu ve miyofibroblasta diferansiyasyonunu inhibe edici etkinliğin de önemli rolü olabileceği düşünülmüştür. Tedavi sırasında proteinüri, hiperlipidemi, albumin düzeyi gibi parametrelerde anlamlı düzelmelerin 1. aydan itibaren başlamakta olduğu ve anlamlı düzelmenin tedavi süresince devam ettiği gözlendi. Hastaların serum kreatinin düzeylerinde çalışma süresince önemli farklılık görülmedi ve MMF'ye bağlı oluşabildiği bildirilen gastroin-testinal ve miyelosupressif yan etkiler gözlenmedi. Sonuç olarak böbrek fonksiyonları normal olan MPGN'li hastaların tedavisinde düşük doz steroid ile birlikte ya da yalnız başına MMF verilmesi, bu retrospektif çalışmaya göre cesaret verici görünmektedir.
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REFERENCES

References: 

1. Badid C, Vincent M, et al: Mycophenolate mofetil redu-ces interstitial myofibroblast infiltration and collagen III depozit. Kidney Int., 58:51(2000).
2. Blaheta RA, Leckel K, et al: Inhibition of endothelial re-ceptor expression and of T-cell ligand activity by mycophenolate mofetil. Transpl. Immunol., 6:251 (1998).
3. Faik RJ, Jennette JC, Nachman PH: Primary Glomerular Disease, Brenner and Rector's The Kidney, Sixtlı Editi-on, (2000) s. 1272.
4. Briggs WA, Choi MJ, et al: Successful mycophenolate mofetil treatment of glomerular disease. Am. J. Kidney Dis. 31:213 (1998).
5. Briggs WA, Choi MJ, et al: Follow-up on mycophenolate mofetil treatment of glomerular disease. Am. J. Kidney Dis. 31:898(1998).
6. Cameron JS, Tumer DR: Idiopathic mesangiocapillary glomerulonephritis. Comparison of types I and II in children and adults and long-term prognosis. Am J Med., 74: 175 (1983)
7. Cattran DC Cardella CJ: Results of a controlled drug trial in membranoproliferative glomerulonephritis. Kidney Int., 27: 436 (1985)
8. Cattran DC: Current status of cyclosporin A in the treatment of membranous, IgA and membranoproliferative glomerulonephritis. Clin Nephrol., (1991) S: 43.
Primer Membranoproliferatif Glomerulonefrit Tedavisinde Mikofenolat Mofetil Kullanımı: Retrospektif Değerlendirme
9. Chan TM, Li F, et al: Efficacy of mycophenolate mofetil in patients vvith diffuse proliferative lupus nephritis. Hong Kong-Gııangzhou Nephrology Study Group. N. Engl. J. Med., 343:1156 (2000).
10. Corna D, Morigi M, Mycophenolate mofetil limits renal damage and prolongs life in murine lupus autoimmune dissease. Kidney int., 51:1583 (1997)
11. D'Amico G: Influence of clinical and histological featu-res on actuarial renal survival in adult patients with idiopatine IgA nephropathy, membranous nephropathy, and membranoproliferative glomerulonephritis: survey of the recent literatüre. Am J Kidney Dis., 20: 315 (1992).
12. Dooley MA, Cosio FG, et al: Mycophenolate mofetil therapy in lupus nephritis: clinical observations. J. Am. Soc. Nephrol., 10:833 (1999).
13. Erbay B, Karatan O, et al: The effect of eyelosporine in idiopathic nephrotic syndrome resistant to immunosupp-ressive therapy. Transplant. Proc, 20:292 (1988).
14. Eugui Almquist SJ, Muller CD, et al: Lymphocyte-selec-tive eytostatic and immunosuppressive effects of mycop-henolic acid in vitro: role of deoxyguanosine nucleotide depletion. Scand. J. Immunol., 33: 161 (1991).
15. Fulton B, Markham A, Focus on Mycophenolate Mofetil. Drugs, 51:278 (1996).
16. Gregory CR: Treatment with rapamyein and mycopheno-lic acid reduces arterial intimal thickening produced by mechanical injury and allows endothelial replacement. Transplantation, 59: 655 (1995).
17. Jayne D, Non-transplant uses of Mycophenolate Mofetil. Current Opinion in Nephrology and Hypertension, 8:563 (1999).
18. Jonsson CA, Svensson L: Beneficial effect of the inosine monophosphate dehydrogenase inhibitor mycophenolate mofetil on survival and severity of glomerulonephritis in systemic lupus erythematosus (SLE)-prone MRLlpr/lpr mice. Clin. Exp. Immunol. 116:534 (1999).
19. Orlovvski T, Rancewicz Z: Long-term immunosuppressive therapy of idiopathic membranoproliferative glomerulonephritis. Klin Wochenschr, 66:1019 (1988).
20. Placebo-controlled study of mycophenolate mofetil com-bined vvith eyelosporin and coıticosteroids for prevention of acute rejeetion. European Mycophenolate Mofetil Co-operative Study Group. Lancet, 345:1321 (1995).
21. Ponticelli C, Richard JG: Treatment of Primary Glomerulonephritis. Clinical Nephrology Series, Oxford Uni-versity Press, 1997.
22. Schmitt H, Bohle A: Long-term prognosis of membranoproliferative glomerulonephritis type I. Significance of clinical and morphological parameters: an investigation of 220 cases. Nephron, 55: 242 (1990).
23. Van Bruggen MC, Walgreen B: Attenuation of murine lupus nephritis by mycophenolate mofetil. J. Am. Soc. Nephrol., 9:1407 (1998).
24. Zisvviler R, Steinmann-Niggli K: Mycophenolic acid: a nevv approach to the therapy of experimental mesangial proliferative glomerulonephritis. J. Am. Soc. Nephrol., 9:2055 (1998).

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