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2.
J Alzheimers Dis ; 19(3): 909-14, 2010.
Article in English | MEDLINE | ID: mdl-20157246

ABSTRACT

Mild cognitive impairment is often considered a transitional condition prodromal to Alzheimer's disease. The dissection of genetic risk factors predisposing to mild cognitive impairment is paramount to assess the individual predisposition and reliably evaluate the effectiveness of early therapeutic interventions. We designed a cross-sectional analysis to test whether the occurrence of mild cognitive impairment is influenced by variations of the tau protein gene. The genotypes of seven polymorphisms tagging the major tau haplotypes were assayed on 186 patients with amnestic mild cognitive impairment and 191 unrelated controls. Association study was conducted by logistic regression including APOE genotype and age as covariates. Case-control analysis showed that the common H1 haplotype is significantly overrepresented in patients (OR, 95% CI: 2.31, 1.52-3.51; p<0.001), whereas did not provide positive signals for any of the H1 sub-haplotypes that had been described as associated with Alzheimer inverted exclamation mark s disease. This finding was confirmed when the epsilon4 allele of the APOE gene was taken into account (OR, 95% CI: 2.319, 1.492-3.603; p<0.001). These results firstly suggest that the risk of mild cognitive impairment is influenced by tau protein gene variations and that mild cognitive impairment shares a common genetic background with Alzheimer's disease. They may help elucidating the genetic risk to cognitive decline and designing effective clinical trials.


Subject(s)
Alzheimer Disease/genetics , Cognition Disorders/diagnosis , Cognition Disorders/genetics , Haplotypes/genetics , tau Proteins/genetics , Aged , Alleles , Apolipoproteins E/genetics , Female , Genotype , Humans , Male , Middle Aged , Neuropsychological Tests , Polymorphism, Genetic/genetics , Severity of Illness Index
3.
Aging Clin Exp Res ; 20(6): 593-6, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19179845

ABSTRACT

Amiodarone is a class III antiarrhythmic agent with a long half-life which is used to control atrial and ventricular arrhythmias, including atrial flutter and fibrillation. We describe here the case of an elderly woman (77 years of age) who was hospitalized for acute atrial fibrillation, abdominal pain, and dyspnea. In the Emergency Department, treatment with intravenous amiodarone was begun. The following day, the patient developed acute liver damage; improved liver function occurred following the withdrawal of amiodarone. Complete recovery of liver function was documented after three weeks. Unfortunately, the patient died from a severe infectious disease, with multiple organ failure.


Subject(s)
Amiodarone/adverse effects , Anti-Arrhythmia Agents/adverse effects , Atrial Fibrillation/drug therapy , Chemical and Drug Induced Liver Injury , Aged , Amiodarone/administration & dosage , Anti-Arrhythmia Agents/administration & dosage , Fatal Outcome , Female , Humans , Injections, Intravenous
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