NDT Advance Access originally published online on December 7, 2004
Nephrology Dialysis Transplantation 2005 20(2):336-341; doi:10.1093/ndt/gfh546
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Nephrol Dial Transplant Vol. 20 No. 2 © ERA–EDTA 2004; all rights reserved
Original Article
Mitochondrial tRNALeu(UUR) mutation in a patient with steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis
1 Department of Pediatrics, 2 Department of Human Genetics, 3 Department of Pathology and 4 Department of Nephrology, University Medical Centre Nijmegen, The Netherlands
Correspondence and offprint requests to: J. F. M. Wetzels, Department of Nephrology, University Medical Centre Nijmegen, 6500 HB Nijmegen, The Netherlands. Email: J.Wetzels{at}nier.umcn.nl
Background. The heterogeneity of mitochondrial cytopathies is characteristic for this group of disorders, which preferentially affect the muscle and nerve system. The A3243G transition in the tRNALeu(UUR) gene has been associated with slowly progressive forms of focal segmental glomerulosclerosis (FSGS). Here we present a patient who developed a severe nephrotic syndrome during her first pregnancy, which persisted after delivery, and proved resistant to immunosuppressive therapy. A sister of our patient had developed diabetes mellitus. We analysed the DNA for the presence of the mitochondrial DNA (mtDNA) A3243G transition.
Methods. DNA was isolated from peripheral blood leukocytes and urine sediments. Polymerase chain reaction was performed to amplify the mtDNA. Restriction enzyme analysis was used to detect the presence of the A3243G transition. Quantitative analysis of the A3243G mutation was done using the pyrosequencing technique.
Results. Quantitative analysis revealed a proportion of mutated mtDNA of 30% in the leukocytes and 68% in the urine sediments of the proband. On further analysis, we also found the transition in the mother, the diabetic sister and the daughter of the proband.
Conclusion. MtDNA abnormalities can cause a steroid-resistant nephrotic syndrome, histologically characterized by FSGS. Physicians should be especially mindful of mitochondrial abnormalities when hearing loss, diabetes mellitus or neuromuscular disorders are present in the patient or family members.
Keywords: A3243G mtDNA transition; glomerulosclerosis; heteroplasmy; pregnancy; proteinuria
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  A. L. Frederiksen, T. D. Jeppesen, J. Vissing, M. Schwartz, K. O. Kyvik, O. Schmitz, P. L. Poulsen, and P. H. Andersen High Prevalence of Impaired Glucose Homeostasis and Myopathy in Asymptomatic and Oligosymptomatic 3243A>G Mitochondrial DNA Mutation-Positive Subjects J. Clin. Endocrinol. Metab., August 1, 2009; 94(8): 2872 - 2879. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 A. I Jonckheere, M. Hogeveen, L. Nijtmans, M. van den Brand, A. Janssen, H. Diepstra, F. van den Brandt, B. van den Heuvel, F. Hol, T. Hofste, et al. A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy BMJ Case Reports, January 22, 2009; 2009(jan21_1): bcr0720080504 - bcr0720080504. [Abstract] [Full Text]
|
|
|
|
 |
|
 A.M. Hall, R.J. Unwin, M.G. Hanna, and M.R. Duchen Renal function and mitochondrial cytopathy (MC): more questions than answers? QJM, October 1, 2008; 101(10): 755 - 766. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 A I Jonckheere, M Hogeveen, L G J Nijtmans, M A M van den Brand, A J M Janssen, J H S Diepstra, F C A van den Brandt, L P van den Heuvel, F A Hol, T G J Hofste, et al. A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy J. Med. Genet., March 1, 2008; 45(3): 129 - 133. [Abstract] [Full Text] [PDF]
|
|