Minimal-change disease in adolescents and adults: epidemiology and therapeutic response

被引:21
|
作者
Keskar, Vaibhav [1 ,2 ]
Jamale, Tukaram Ekanath [1 ,2 ]
Jeevanna, Kulkarni Manjunath [3 ]
Jagadish, Pradeep Kiggal [3 ]
Fernandes, Gwendolyn [4 ]
Hase, Niwrutti [1 ,2 ]
机构
[1] Seth GS Med Coll, Dept Nephrol, Bombay, Maharashtra, India
[2] King Edward Mem Hosp, Bombay, Maharashtra, India
[3] Grant Med Coll, Nephrol, Bombay, Maharashtra, India
[4] Seth GS Med Coll, Pathol, Bombay, Maharashtra, India
来源
CLINICAL KIDNEY JOURNAL | 2013年 / 6卷 / 05期
关键词
minimal-change disease in adults; nephrotic syndrome; treatment outcomes;
D O I
10.1093/ckj/sft063
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Epidemiology of minimal-change disease (MCD) in adults differs from that in children and is not studied well in Indian population. Methods. We retrospectively studied the records of 61 adult patients with MCD to assess clinical, laboratory and histopathological features, and to evaluate the response to treatment, course and complications of the disease and therapy. Results. The male to female ratio was 1.17:1. Mean age was 30.46 years. Of the total, 6.55% had hypertension; 13.11% had microhaematuria. After initial treatment with steroids, 68.85% had complete remission (CR) and 13.1% had partial remission (PR). Twelve of 14 (85.71%) steroidresistant cases had CR or PR after alternative immunosuppression with cyclophosphamide, or mycophenolate mofetil. Of all patients, 44.2% had at least one relapse; 8.19% were frequently relapsing and 26.22% were steroid dependent. After a mean follow-up of 149.9 weeks, 38 (61.29%) patients were in CR and 16 (26.22%) in PR with a mean proteinuria of 1.28 g/day, 3 being treated for relapse. Mean serum creatinine was 89.28 ae mol/L (1.01 mg/dL). Fourteen (22.95%) had acute kidney injury (AKI). All but two recovered completely. Conclusions. This single-centre study with a medium-term follow-up shows that majority of patients respond to steroids or alternative immunosuppressants. AKI is common and may not be completely reversible in some cases.
引用
收藏
页码:469 / 472
页数:4
相关论文
共 50 条
  • [1] Coexistence of atheroemboli and minimal-change disease
    Liss, KA
    Gaughan, WJ
    MCCue, PA
    Burke, JF
    CLINICAL NEPHROLOGY, 1997, 47 (02) : 125 - 128
  • [2] Minimal-change disease secondary to etanercept
    Koya, Mariko
    Pichler, Raimund
    Jefferson, J. Ashley
    CLINICAL KIDNEY JOURNAL, 2012, 5 (05): : 420 - 423
  • [3] Kimura's disease and minimal-change nephrotic syndrome
    Sud, K
    Saha, T
    Das, A
    Kakkar, N
    Jha, V
    Kohli, HS
    Sakhuja, V
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 1996, 11 (07) : 1349 - 1351
  • [4] Gross hematuria in minimal-change disease nephrotic syndrome
    Lavjay Butani
    Pediatric Nephrology, 2006, 21 : 1783 - 1783
  • [5] THYMOMA AND MINIMAL-CHANGE GLOMERULONEPHRITIS
    MCDONALD, P
    KALRA, PA
    COWARD, RA
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 1992, 7 (04) : 357 - 359
  • [6] Minimal-change disease as a paraneoplastic syndrome in a patient with ovarian carcinoma
    Gonzalez-Fontal, Guido R.
    Restrepo, Juan G.
    Henao-Martinez, Andres F.
    CLINICAL KIDNEY JOURNAL, 2011, 4 (06): : 427 - 429
  • [7] Minimal-change nephropathy and malignant thymoma
    Zinger, C
    Ben-Itzhak, O
    Szylman, P
    Green, J
    Nakhoul, F
    AMERICAN JOURNAL OF NEPHROLOGY, 1998, 18 (01) : 61 - 63
  • [8] Minimal-change renal disease and Graves' disease: a case report and literature review
    Hasnain, Wirasat
    Stillman, Isaac E.
    Bayliss, George P.
    CLINICAL KIDNEY JOURNAL, 2011, 4 (01): : 96 - 98
  • [9] Cyclooxygenase-2 inhibitor-associated minimal-change disease
    Almansori, M
    Kovithavongs, T
    Qarni, MU
    CLINICAL NEPHROLOGY, 2005, 63 (05) : 381 - 384
  • [10] Minimal-change glomerulonephritis associated with infantile autosomal recessive polycystic kidney disease
    Banyai, S
    Falger, J
    Haag-Weber, M
    Horl, WH
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 1997, 12 (12) : 2726 - 2727