Skip to main content

Mitochondrial Respiratory Chain Hepatopathies: Role of Liver Transplantation. A Case Series of Five Patients

  • Case Report
  • Chapter
  • First Online:
JIMD Reports - Case and Research Reports, 2012/1

Abstract

Introduction: Orthotopic liver transplantation (OLT) in patients with mitochondrial respiratory chain disorders (MRCD) is controversial because of possible multi-organ involvement.

Aim: To illustrate the clinical diversity of MRCD, the difficulty in making an accurate tissue diagnosis and whether to undertake OLT in five patients with proven MRCD. A review of the reported cases in the literature is presented.

Methods: Retrospective chart review from 1995 to 2007 at a paediatric liver transplant centre where five children with hepatic MRCD were identified.

Results: Patient 1 was transplanted for ‘cryptogenic’ cirrhosis. The diagnosis of MRCD was made on the explant. The patient remains well 5 years after transplant. Patient 2 presented with fulminant liver failure at 3 months of age. Although no extrahepatic manifestations were identified, OLT was not considered. Patient 3 presented with recurrent hypoglycaemia and was transplanted for fulminant hepatic failure at 12 months of age. He died of pulmonary hypertension 9 months post OLT. Patient 4 was diagnosed with MRCD at the age of 2 years. Death occurred at the age of 14 years, while listed for combined liver–kidney transplant, after a stroke-like episode following severe sepsis. Patient 5 developed liver failure after valproic acid was instituted for seizures. Mitochondrial DNA depletion syndrome was diagnosed and transplantation was not offered.

Conclusion: Hepatic MRCD has a variable presentation. Diagnosis requires the measurement of respiratory chain enzymes on tissue from liver biopsy. Whether to proceed to OLT is a difficult decision given a good outcome in a minority of cases, suggesting that MRCD should not be an absolute contraindication to liver transplantation.

Competing interests: None declared.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Barclay AR, Sholler G, Christodolou J, Shun A, Arbuckle S, Dorney S et al (2005) Pulmonary hypertension–a new manifestation of mitochondrial disease. J Inherit Metab Dis 28(6):1081–1089

    Article  PubMed  CAS  Google Scholar 

  • Cormier-Daire V, Chretien D, Rustin P, Rotig A, Dubuisson C, Jacquemin E et al (1997) Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylation. J Pediatr 130(5):817–822

    Article  PubMed  CAS  Google Scholar 

  • Delarue A, Paut O, Guys JM, Montfort MF, Lethel V, Roquelaure B et al (2000) Inappropriate liver transplantation in a child with Alpers-Huttenlocher syndrome misdiagnosed as valproate-induced acute liver failure. Pediatr Transplant 4(1):67–71

    Article  PubMed  CAS  Google Scholar 

  • DiMauro S, Schon EA (2003) Mitochondrial respiratory-chain diseases. N Engl J Med 348(26):2656–2668

    Article  PubMed  CAS  Google Scholar 

  • Dimmock DP, Zhang Q, Dionisi-Vici C, Carrozzo R, Shieh J, Tang LY et al (2008) Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase. Hum Mutat 29(2):330–331

    Article  PubMed  CAS  Google Scholar 

  • Ds K (2010) Treatment of mitochondrial electron transport chain disorders: a review of clinical trials over the past decade. Mol Genet Metab 99(3):246–255

    Article  Google Scholar 

  • Dubern B, Broue P, Dubuisson C, Cormier-Daire V, Habes D, Chardot C et al (2001) Orthotopic liver transplantation for mitochondrial respiratory chain disorders: a study of 5 children. Transplantation 71(5):633–637

    Article  PubMed  CAS  Google Scholar 

  • Ducluzeau PH, Lachaux A, Bouvier R, Duborjal H, Stepien G, Bozon D et al (2002) Progressive reversion of clinical and molecular phenotype in a child with liver mitochondrial DNA depletion. J Hepatol 36(5):698–703

    Article  PubMed  Google Scholar 

  • Durand P, Debray D, Mandel R, Baujard C, Branchereau S, Gauthier F et al (2001) Acute liver failure in infancy: a 14-year experience of a pediatric liver transplantation center. J Pediatr 139(6):871–876

    Article  PubMed  CAS  Google Scholar 

  • Freckmann ML, Thorburn DR, Kirby DM, Kamath KR, Hammond J, Dennett X et al (1997) Mitochondrial electron transport chain defect presenting as hypoglycemia. J Pediatr 130(3):431–436

    Article  PubMed  CAS  Google Scholar 

  • Freisinger P, Futterer N, Lankes E, Gempel K, Berger TM, Spalinger J et al (2006) Hepatocerebral mitochondrial DNA depletion syndrome caused by deoxyguanosine kinase (DGUOK) mutations. Arch Neurol 63(8):1129–1134

    Article  PubMed  Google Scholar 

  • Gillis LASR (2003) Gastrointestinal manifestations of mitochondrial disease. Gastroenterol Clin North Am 32(3):789–817

    Article  PubMed  Google Scholar 

  • Goncalves I, Hermans D, Chretien D, Rustin P, Munnich A, Saudubray JM et al (1995) Mitochondrial respiratory chain defect: a new etiology for neonatal cholestasis and early liver insufficiency. J Hepatol 23(3):290–294

    PubMed  CAS  Google Scholar 

  • Hakonen AHDG, Salemi R, Bindoff LA, Van Goethem G, DiMauro S, Thorburn DR, Suomalainen A (2007) Abundance of the POLG disease mutations in Europe, Australia, New Zealand, and the USA explained by single ancient European founders. Eur J Hum Genet 15:779–783

    Article  PubMed  CAS  Google Scholar 

  • Kaji S, Murayama K, Nagata I, Nagasaka H, Takayanagi M, Ohtake A et al (2009) Fluctuating liver functions in siblings with MPV17 mutations and possible improvement associated with dietary and pharmaceutical treatments targeting respiratory chain complex II. Mol Genet Metab 97(4):292–296

    Article  PubMed  CAS  Google Scholar 

  • Kamath BM, Olthoff KM (2010) Liver transplantation in children: update 2010. Pediatr Clin North Am 57(2):401–414, table of contents

    Google Scholar 

  • Kayihan N, Nennesmo I, Ericzon BG, Nemeth A (2000) Fatal deterioration of neurological disease after orthotopic liver transplantation for valproic acid-induced liver damage. Pediatr Transplant 4(3):211–214

    Article  PubMed  CAS  Google Scholar 

  • Kirby DM, Thorburn DR (2008) Approaches to finding the molecular basis of mitochondrial oxidative phosphorylation disorders. Twin Res Hum Genet 11(4):395–411

    Article  PubMed  Google Scholar 

  • Lee WS, Sokol RJ (2007) Liver disease in mitochondrial disorders. Semin Liver Dis 27(3):259–273

    Article  PubMed  CAS  Google Scholar 

  • Mancuso M, Ferraris S, Pancrudo J, Feigenbaum A, Raiman J, Christodoulou J et al (2005) New DGK gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndrome. Arch Neurol 62(5):745–747

    Article  PubMed  Google Scholar 

  • Mandel H, Hartman C, Berkowitz D, Elpeleg ON, Manov I, Iancu TC (2001) The hepatic mitochondrial DNA depletion syndrome: ultrastructural changes in liver biopsies. Hepatology 34(4 Pt 1):776–784

    Article  PubMed  CAS  Google Scholar 

  • Munnich A, Rotig A, Chretien D, Saudubray JM, Cormier V, Rustin P (1996) Clinical presentations and laboratory investigations in respiratory chain deficiency. Eur J Pediatr 155(4):262–274

    Article  PubMed  CAS  Google Scholar 

  • Nguyen KV, Sharief FS, Chan SS, Copeland WC, Naviaux RK (2006) Molecular diagnosis of Alpers syndrome. J Hepatol 45(1):108–116

    Article  PubMed  CAS  Google Scholar 

  • Rabinowitz SS, Gelfond D, Chen CK, Gloster ES, Whitington PF, Sacconi S et al (2004) Hepatocerebral mitochondrial DNA depletion syndrome: clinical and morphologic features of a nuclear gene mutation. J Pediatr Gastroenterol Nutr 38(2):216–220

    Article  PubMed  Google Scholar 

  • Rake JP, van Spronsen FJ, Visser G, Ruitenbeek W, Schweizer JJ, Bijleveld CM et al (2000) End-stage liver disease as the only consequence of a mitochondrial respiratory chain deficiency: no contra-indication for liver transplantation. Eur J Pediatr 159(7):523–526

    Article  PubMed  CAS  Google Scholar 

  • Salviati L, Sacconi S, Mancuso M, Otaegui D, Camano P, Marina A et al (2002) Mitochondrial DNA depletion and dGK gene mutations. Ann Neurol 52(3):311–317

    Article  PubMed  CAS  Google Scholar 

  • Scheers I, Bachy V, Stephenne X, Sokal EM (2005) Risk of hepatocellular carcinoma in liver mitochondrial respiratory chain disorders. J Pediatr 146(3):414–417

    Article  PubMed  Google Scholar 

  • Slama A, Giurgea I, Debrey D, Bridoux D, de Lonlay P, Levy P et al (2005) Deoxyguanosine kinase mutations and combined deficiencies of the mitochondrial respiratory chain in patients with hepatic involvement. Mol Genet Metab 86(4):462–465

    Article  PubMed  CAS  Google Scholar 

  • Sokal EM, Sokol R, Cormier V, Lacaille F, McKiernan P, Van Spronsen FJ et al (1999) Liver transplantation in mitochondrial respiratory chain disorders. Eur J Pediatr 158(Suppl 2):S81–S84

    Article  PubMed  Google Scholar 

  • Sokol RJTW (1999) Mitochondria and childhood liver diseases. J Pediatr Gastroenterol Nutr 28(1):4–16

    Article  PubMed  CAS  Google Scholar 

  • Tadiboyina VT, Rupar A, Atkison P, Feigenbaum A, Kronick J, Wang J et al (2005) Novel mutation in DGUOK in hepatocerebral mitochondrial DNA depletion syndrome associated with cystathioninuria. Am J Med Genet A 135(3):289–291

    Article  PubMed  Google Scholar 

  • Thomson M, McKiernan P, Buckels J, Mayer D, Kelly D (1998) Generalised mitochondrial cytopathy is an absolute contraindication to orthotopic liver transplant in childhood. J Pediatr Gastroenterol Nutr 26(4):478–481

    Article  PubMed  CAS  Google Scholar 

  • Tzoulis C, Engelsen BA, Telstad W, Aasly J, Zeviani M, Winterthun S et al (2006) The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases. Brain 129(Pt 7):1685–1692

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

Simone Tregoning, Adrienne Laskowski, Jaclyn Sceneay, and Dr Denise Kirby are thanked for assistance with MRCD studies. We thank Prof Robert Taylor for mtDNA sequencing. Associate Professor David Thorburn is supported by an Australian National Health & Medical Research Council Principal Research Fellowship.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Michael O Stormon .

Editor information

Editors and Affiliations

Additional information

Communicated by: Garry Brown.

Rights and permissions

Reprints and permissions

Copyright information

© 2011 SSIEM and Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

De Greef, E. et al. (2011). Mitochondrial Respiratory Chain Hepatopathies: Role of Liver Transplantation. A Case Series of Five Patients. In: JIMD Reports - Case and Research Reports, 2012/1. JIMD Reports, vol 4. Springer, Berlin, Heidelberg. https://doi.org/10.1007/8904_2011_29

Download citation

  • DOI: https://doi.org/10.1007/8904_2011_29

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-25751-3

  • Online ISBN: 978-3-642-25752-0

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics