Key result
Cerebrovascular metabolism genotypes (APOE, ACE, LDLR, CETP, NR1H2) were associated with differences in age of onset and neuropsychiatric symptoms among 201 patients with late-onset Alzheimer's.
Why the study?
Are cerebrovascular metabolism genotypes associated with age at onset and neuropsychiatric symptoms in patients with late-onset Alzheimer's disease dementia?
Observational (n=201)
Are cerebrovascular metabolism genotypes associated with age at onset and neuropsychiatric symptoms in patients with late-onset Alzheimer's disease dementia?
Cerebrovascular metabolism genotypes, particularly APOE, ACE, LDLR, CETP, and NR1H2, are associated with distinct neuropsychiatric symptom profiles in late-onset Alzheimer's disease.
Hypothesis-generating for genotype-phenotype links in late-onset Alzheimer's; leaves open clinical utility pending validation.
OBJECTIVE:: To study associations of cerebrovascular metabolism genotypes and haplotypes with age at Alzheimer's disease dementia (AD) onset and with neuropsychiatric symptoms according to each dementia stage. METHODS:: Consecutive outpatients with late-onset AD were assessed for age at dementia onset and Neuropsychiatric Inventory scores according to Clinical Dementia Rating scores, apolipoprotein E gene (APOE) haplotypes, angiotensin-converting enzyme gene (ACE) variants rs1800764 and rs4291, low-density lipoprotein cholesterol receptor gene (LDLR) variants rs11669576 and rs5930, cholesteryl ester transfer protein gene (CETP) variants I422V and TaqIB, and liver X receptor beta gene (NR1H2) polymorphism rs2695121. RESULTS:: Considering 201 patients, only APOE-ɛ4 carriers had earlier dementia onset in multiple correlations, as well as less apathy, more delusions, and more aberrant motor behavior. Both ACE polymorphisms were associated with less intense frontally mediated behaviors. Regarding LDLR variants, carriers of the A allele of rs11669576 had less anxiety and more aberrant motor behavior, whereas carriers of the A allele of rs5930 had less delusions, less anxiety, more apathy, and more irritability. CETP variants that included G alleles of I422V and TaqIB were mostly associated with less intense frontally mediated behaviors, while severely impaired carriers of the T allele of rs2695121 had more anxiety and more aberrant motor behavior. CONCLUSION:: Though only APOE haplotypes affected AD onset, cerebrovascular metabolism genotypes were associated with differences in several neuropsychiatric manifestations of AD.
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Oliveira et al. (2017) conducted an observational in Late-onset Alzheimer's disease dementia (n=201). Cerebrovascular metabolism genotypes was evaluated on Age at dementia onset and Neuropsychiatric Inventory scores. Cerebrovascular metabolism genotypes (APOE, ACE, LDLR, CETP, NR1H2) were associated with differences in age of onset and neuropsychiatric symptoms among 201 patients with late-onset Alzheimer's.
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