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DOI 10.1136/jclinpath-2011-200005

Медицинская библиотека · Journal of clinical pathology · 2011

Predictive factors for ciclosporin-associated nephrotoxicity in children with minimal change nephrotic syndrome.

Kim Ji Hong, Park Se Jin, Yoon So Jin, Lim Beom Jin, Jeong Hyeon Joo, Lee Jae Seung, Kim Pyung Kil, Shin Jae Il

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Аннотация

AIMS: To identify the predictive factors for ciclosporin A (CyA)-associated nephrotoxicity (CAN) in children with minimal change nephrotic syndrome (MCNS).

METHODS

The clinical and laboratory findings of 58 children (median age 3.2 years, range 1.1-13.1 years, male:female 48:10) with MCNS who were treated with CyA from 1992 to 2002 were analysed retrospectively. Forty-eight (83%) of them were steroid dependent and 10 (17%) were steroid resistant. The starting dose of CyA was 5mg/kg per day, and the desired drug level was kept at 100-200 ng/ml. Serial renal biopsies were performed before and after CyA therapy.

RESULTS

Twenty-two patients (38%) had CAN (group I) and 36 (62%) did not (group II). There were no differences in the age at onset, sex, initial response to steroids, duration of CyA therapy and relapse rates. However, the median CyA trough levels were significantly higher in group I than in group II (218.0±15.2 vs 171.8±6.7 ng/ml, p=0.01). Changes in creatinine clearance were more decreased in group I than in group II (-39.4±8.2 vs 2.7±4.3 ml/min per 1.73m(2), p<0.0001). Multiple logistic regression analysis also revealed the median CyA trough level was an independent risk factor for the development of CAN (OR 1.025, 95% CI 1.007 to 1.044, p=0.007).

CONCLUSIONS

The median CyA trough level was an independent and significant risk factor for the development of CAN in children with MCNS receiving moderate-dose CyA.

Для цитирования: Kim Ji Hong, Park Se Jin, Yoon So Jin, Lim Beom Jin, Jeong Hyeon Joo, Lee Jae Seung, Kim Pyung Kil, Shin Jae Il. Predictive factors for ciclosporin-associated nephrotoxicity in children with minimal change nephrotic syndrome.. Journal of clinical pathology. 2011. DOI: 10.1136/jclinpath-2011-200005.

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