Document Detail


Primary carnitine deficiency and pivalic acid exposure causing encephalopathy and fatal cardiac events.
MedLine Citation:
PMID:  22566287     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
BACKGROUND: Several episodes of sudden death among young Faroese individuals have been associated with primary carnitine deficiency (PCD). Patients suffering from PCD have low carnitine levels and can present with metabolic and/or cardiac complications. Pivalic acid exposure decreases carnitine levels. The purpose of this study was to investigate and describe the association and pathophysiology of exposure to antibiotics containing pivalic acid and severe neurological and cardiac complications in six identified subjects suffering from PCD. METHODS AND MATERIALS: Six cases of PCD were identified and studied through medical records and family interview. Stored biomaterial was analyzed for mutations causing PCD. RESULTS: Five patients (two children, three adults) died suddenly while one adult patient survived sudden cardiac arrest. Lethal cardiac arrhythmia was documented in five patients, while one patient was not monitored at time of death, but had signs of cardiac arrhythmia a few days earlier. All patients suffered encephalopathy before cardiac arrhythmia. Autopsy showed severe hepatic steatosis and signs of cerebral edema in four out of five. One subject had a dilated heart. All patients were homozygous for the c.95A>G (p.N32S) mutation in SLC22A5 causing PCD. All patients had been treated with antibiotics containing pivalic acid prior to the episode. CONCLUSION: Exposure to antibiotics containing pivalic acid was associated with encephalopathy and progression to lethal cardiac arrhythmia in patients suffering from PCD.
Authors:
Jan Rasmussen; Olav W Nielsen; Allan M Lund; Lars Køber; Høgni Djurhuus
Related Documents :
12408257 - Multiple av nodal pathways in patients with av nodal reentrant tachycardia--more common...
20063297 - Long-term outcome of atrial synchronous mode pacing in patients with atrioventricular b...
1199947 - Congenital and surgical atrioventricular block within the his bundle.
22971467 - Ccsvi is associated with multiple sclerosis.
12682167 - Molecular analysis of staphylococcus aureus blood isolates shows lack of polyclonal bac...
11054347 - Pauci-immune renal vasculitis: natural history, prognostic factors, and impact of therapy.
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-5-8
Journal Detail:
Title:  Journal of inherited metabolic disease     Volume:  -     ISSN:  1573-2665     ISO Abbreviation:  -     Publication Date:  2012 May 
Date Detail:
Created Date:  2012-5-8     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7910918     Medline TA:  J Inherit Metab Dis     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Department of Internal Medicine, National Hospital, FO-100, Thorshavn, the Faroe Islands, lsjanra@ls.fo.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Impact of severity of renal dysfunction on determinants of in-hospital mortality among patients unde...
Next Document:  The meaning and use of spirituality among African American women living with HIV/AIDS.