Effect of the XbaI polymorphism of estrogen receptor alpha on postmenopausal gray matter

The frequent polymorphism XbaI (A351G) in the estrogen receptor alpha (ERalpha) gene has been associated with some postmenopausal pathologies’ risk such as Alzheimer's disease (AD) or cognitive decline. In the present study, we explored whether the XbaI polymorphism leads to different gray matt...

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Published inNeuroscience letters Vol. 434; no. 3; pp. 304 - 309
Main Authors Boccardi, Marina, Scassellati, Catia, Ghidoni, Roberta, Testa, Cristina, Benussi, Luisa, Bonetti, Matteo, Bocchio-Chiavetto, Luisella, Gennarelli, Massimo, Binetti, Giuliano, Frisoni, Giovanni B.
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Published Ireland Elsevier Ireland Ltd 04.04.2008
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Abstract The frequent polymorphism XbaI (A351G) in the estrogen receptor alpha (ERalpha) gene has been associated with some postmenopausal pathologies’ risk such as Alzheimer's disease (AD) or cognitive decline. In the present study, we explored whether the XbaI polymorphism leads to different gray matter volumes using voxel-based morphometry (VBM) on 20 magnetic resonance images of healthy postmenopausal women. Subjects carrying the less common XbaI/X allele were contrasted to non-carriers in groups well balanced by relevant confounding variables. The XbaI/X allele carriers displayed clusters ranging from 9 to 28% of tissue reductions in the cerebellar (cluster size, z, stereotactic coordinates: 16 mm 3; 3.17; 14, −94, −38) and cerebral cortex, in particular in the occipital lobe (272 mm 3; 3.76; −38,−68,−16), in the middle frontal gyrus (192 mm 3; 3.71; 38, 12, 38) and in the middle temporal gyrus, while the opposite comparison was negative. The XbaI/X allele in ERalpha gene is associated to smaller gray matter volumes of the cerebral and cerebellar cortex. This allele might increase the susceptibility for senile neurodegenerative conditions, being associated to smaller cerebral reserve.
AbstractList The frequent polymorphism XbaI (A351G) in the estrogen receptor alpha (ERalpha) gene has been associated with some postmenopausal pathologies' risk such as Alzheimer's disease (AD) or cognitive decline. In the present study, we explored whether the XbaI polymorphism leads to different gray matter volumes using voxel-based morphometry (VBM) on 20 magnetic resonance images of healthy postmenopausal women. Subjects carrying the less common XbaI/X allele were contrasted to non-carriers in groups well balanced by relevant confounding variables. The XbaI/X allele carriers displayed clusters ranging from 9 to 28% of tissue reductions in the cerebellar (cluster size, z, stereotactic coordinates: 16 mm(3); 3.17; 14, -94, -38) and cerebral cortex, in particular in the occipital lobe (272 mm(3); 3.76; -38,-68,-16), in the middle frontal gyrus (192 mm(3); 3.71; 38, 12, 38) and in the middle temporal gyrus, while the opposite comparison was negative. The XbaI/X allele in ERalpha gene is associated to smaller gray matter volumes of the cerebral and cerebellar cortex. This allele might increase the susceptibility for senile neurodegenerative conditions, being associated to smaller cerebral reserve.
The frequent polymorphism XbaI (A351G) in the estrogen receptor alpha (ERalpha) gene has been associated with some postmenopausal pathologies' risk such as Alzheimer's disease (AD) or cognitive decline. In the present study, we explored whether the XbaI polymorphism leads to different gray matter volumes using voxel-based morphometry (VBM) on 20 magnetic resonance images of healthy postmenopausal women. Subjects carrying the less common XbaI/X allele were contrasted to non-carriers in groups well balanced by relevant confounding variables. The XbaI/X allele carriers displayed clusters ranging from 9 to 28% of tissue reductions in the cerebellar (cluster size, z, stereotactic coordinates: 16 mm(3); 3.17; 14, -94, -38) and cerebral cortex, in particular in the occipital lobe (272 mm(3); 3.76; -38,-68,-16), in the middle frontal gyrus (192 mm(3); 3.71; 38, 12, 38) and in the middle temporal gyrus, while the opposite comparison was negative. The XbaI/X allele in ERalpha gene is associated to smaller gray matter volumes of the cerebral and cerebellar cortex. This allele might increase the susceptibility for senile neurodegenerative conditions, being associated to smaller cerebral reserve.The frequent polymorphism XbaI (A351G) in the estrogen receptor alpha (ERalpha) gene has been associated with some postmenopausal pathologies' risk such as Alzheimer's disease (AD) or cognitive decline. In the present study, we explored whether the XbaI polymorphism leads to different gray matter volumes using voxel-based morphometry (VBM) on 20 magnetic resonance images of healthy postmenopausal women. Subjects carrying the less common XbaI/X allele were contrasted to non-carriers in groups well balanced by relevant confounding variables. The XbaI/X allele carriers displayed clusters ranging from 9 to 28% of tissue reductions in the cerebellar (cluster size, z, stereotactic coordinates: 16 mm(3); 3.17; 14, -94, -38) and cerebral cortex, in particular in the occipital lobe (272 mm(3); 3.76; -38,-68,-16), in the middle frontal gyrus (192 mm(3); 3.71; 38, 12, 38) and in the middle temporal gyrus, while the opposite comparison was negative. The XbaI/X allele in ERalpha gene is associated to smaller gray matter volumes of the cerebral and cerebellar cortex. This allele might increase the susceptibility for senile neurodegenerative conditions, being associated to smaller cerebral reserve.
The frequent polymorphism XbaI (A351G) in the estrogen receptor alpha (ERalpha) gene has been associated with some postmenopausal pathologies’ risk such as Alzheimer's disease (AD) or cognitive decline. In the present study, we explored whether the XbaI polymorphism leads to different gray matter volumes using voxel-based morphometry (VBM) on 20 magnetic resonance images of healthy postmenopausal women. Subjects carrying the less common XbaI/X allele were contrasted to non-carriers in groups well balanced by relevant confounding variables. The XbaI/X allele carriers displayed clusters ranging from 9 to 28% of tissue reductions in the cerebellar (cluster size, z, stereotactic coordinates: 16 mm 3; 3.17; 14, −94, −38) and cerebral cortex, in particular in the occipital lobe (272 mm 3; 3.76; −38,−68,−16), in the middle frontal gyrus (192 mm 3; 3.71; 38, 12, 38) and in the middle temporal gyrus, while the opposite comparison was negative. The XbaI/X allele in ERalpha gene is associated to smaller gray matter volumes of the cerebral and cerebellar cortex. This allele might increase the susceptibility for senile neurodegenerative conditions, being associated to smaller cerebral reserve.
Author Boccardi, Marina
Bonetti, Matteo
Ghidoni, Roberta
Frisoni, Giovanni B.
Scassellati, Catia
Testa, Cristina
Gennarelli, Massimo
Binetti, Giuliano
Bocchio-Chiavetto, Luisella
Benussi, Luisa
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Snippet The frequent polymorphism XbaI (A351G) in the estrogen receptor alpha (ERalpha) gene has been associated with some postmenopausal pathologies’ risk such as...
The frequent polymorphism XbaI (A351G) in the estrogen receptor alpha (ERalpha) gene has been associated with some postmenopausal pathologies' risk such as...
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SubjectTerms Alzheimer Disease - genetics
Alzheimer Disease - metabolism
Alzheimer Disease - physiopathology
Atrophy - genetics
Atrophy - metabolism
Atrophy - physiopathology
Brain - metabolism
Brain - pathology
Brain - physiopathology
Cognition Disorders - genetics
Cognition Disorders - metabolism
Cognition Disorders - physiopathology
Cytoprotection - genetics
Dementia - genetics
Dementia - metabolism
Dementia - physiopathology
Deoxyribonucleases, Type II Site-Specific
Disease Progression
DNA Mutational Analysis
Estrogen receptor alpha
Estrogen Receptor alpha - genetics
Estrogens - metabolism
Female
Gene Frequency
Genetic Predisposition to Disease - genetics
Genetic Testing
Genotype
Heterozygote
Humans
Magnetic Resonance Imaging
Middle Aged
Morphometry
Neuroimaging
Polymorphism, Genetic - genetics
Polymorphism, Restriction Fragment Length
Postmenopause - metabolism
VBM
XbaI
Title Effect of the XbaI polymorphism of estrogen receptor alpha on postmenopausal gray matter
URI https://dx.doi.org/10.1016/j.neulet.2008.01.076
https://www.ncbi.nlm.nih.gov/pubmed/18342444
https://www.proquest.com/docview/70432503
Volume 434
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