HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The urinary proteome and metabonome differ from normal in adults with mitochondrial disease.

Abstract
We studied the extent and nature of renal involvement in a cohort of 117 adult patients with mitochondrial disease, by measuring urinary retinol-binding protein (RBP) and albumin; established markers of tubular and glomerular dysfunction, respectively. Seventy-five patients had the m.3243A>G mutation and the most frequent phenotypes within the entire cohort were 14 with MELAS, 33 with MIDD, and 17 with MERRF. Urinary RBP was increased in 29 of 75 of m.3243A>G patients, whereas albumin was increased in 23 of the 75. The corresponding numbers were 16 and 14, respectively, in the 42 non-m.3243A>G patients. RBP and albumin were higher in diabetic m.3243A>G patients than in nondiabetics, but there were no significant differences across the three major clinical phenotypes. The urine proteome (mass spectrometry) and metabonome (nuclear magnetic resonance) in a subset of the m.3243A>G patients were markedly different from controls, with the most significant alterations occurring in lysosomal proteins, calcium-binding proteins, and antioxidant defenses. Differences were also found between asymptomatic m.3243A>G carriers and controls. No patients had an elevated serum creatinine level, but 14% had hyponatremia, 10% had hypophosphatemia, and 14% had hypomagnesemia. Thus, abnormalities in kidney function are common in adults with mitochondrial disease, exist in the absence of elevated serum creatinine, and are not solely explained by diabetes.
AuthorsAndrew M Hall, Annalisa Vilasi, Isabel Garcia-Perez, Marta Lapsley, Charlotte L Alston, Robert D S Pitceathly, Robert McFarland, Andrew M Schaefer, Doug M Turnbull, Nick J Beaumont, Justin J Hsuan, Pedro R Cutillas, John C Lindon, Elaine Holmes, Robert J Unwin, Robert W Taylor, Grainne S Gorman, Shamima Rahman, Michael G Hanna
JournalKidney international (Kidney Int) Vol. 87 Issue 3 Pg. 610-22 (Mar 2015) ISSN: 1523-1755 [Electronic] United States
PMID25207879 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antioxidants
  • Biomarkers
  • Calcium-Binding Proteins
  • Proteins
  • Proteome
  • Retinol-Binding Proteins
  • lysosomal proteins
  • RNA, Transfer
  • Creatinine
  • Magnesium
Topics
  • Adolescent
  • Adult
  • Aged
  • Albuminuria (urine)
  • Antioxidants (metabolism)
  • Biomarkers (urine)
  • Calcium-Binding Proteins (urine)
  • Case-Control Studies
  • Creatinine (blood, urine)
  • Cross-Sectional Studies
  • Deafness (complications, genetics, urine)
  • Diabetes Mellitus, Type 2 (complications, genetics, urine)
  • Heterozygote
  • Humans
  • Hyponatremia (etiology)
  • Hypophosphatemia (etiology)
  • Kidney Diseases (complications, urine)
  • MELAS Syndrome (complications, genetics, urine)
  • MERRF Syndrome (complications, genetics, urine)
  • Magnesium (blood)
  • Metabolome
  • Middle Aged
  • Mitochondrial Diseases (complications, genetics, urine)
  • Mutation
  • Proteins (metabolism)
  • Proteome
  • RNA, Transfer
  • Retinol-Binding Proteins (urine)
  • Young Adult

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: