Is responsible for neuronal aging and degeneration [21]. Increased vulnerability to Bcl-2related apoptosis induced by physiological stressors has been suggested to contribute to the reductions in regional cerebral volumes, neurons, and glial cells in patients with mood disorders [22]. An investigation of the Tunicamycin site genetic effect of the Bcl-2 
rs956572 polymorphism on regional brain-GM volumes in adults aged 19 to 60 years using optimized voxel-based morphometry (VBM) showed that G homozygotes get Calcitonin (salmon) displayed larger GM volumes in the left ventral striatum, compared with that of the A-allele carriers [23]. Recently, we investigated the genetic effects of Bcl-2 rs956572 on regional GM volumes in elderly men [24]. We found that G homozygotes had significantly larger GM volumes in the left precuneus, the right lingual gyrus, and the left superior occipital gyrus, compared with those of the A-allele carriers. Previous studies have reported age-related influences on Bcl-2 expression in specific brain regions [25,26]. Thus, increased vulnerability to Bcl-2-related apoptosis may be involved in the aging process [27]. Considering these findings and the role that Bcl-2 plays in neural plasticity and cellular resilience, we hypothesized that the Bcl-2 rs956572 allelic variant may contribute to age-related changes in GM volumes. Therefore, we evaluated the relationship between the Bcl-2 rs956572 genotype and age-related changes in regional GM volumes based on the results of optimized VBM over a broad age range.including malignancy, heart failure, lung disease, and diabetes; and (6) a Clinical Dementia Rating Scale score over 0.5 for participants aged 65 and over. The cognitive functioning of the participants was evaluated using the MMSE and the Wechsler Digit Span Task tests. All participants had sufficient visual and auditory acuity to undergo cognitive testing. The 30-point MMSE cognitive test was designed for screening cognitive impairment in cross-cultural studies. Our research was conducted in accordance with the Declaration of Helsinki, and was approved by the Institutional Review Board of Taipei Veterans General Hospital. Written, informed consent was 23727046 obtained from all the participants.2.2 GenotypingGenomic DNA was extracted from peripheral blood with a commercial kit (Qiagen, Gentra Puregene Blood Kit). Genotyping procedures for identifying the rs956572 was performed by the polymerase chain reaction (PCR)-restriction fragment length polymorphism method. The following PCR primers, which 
were synthesized by MISSION BIOTECH Co. (Taiwan) were used in the present study: forward, 5- AGAGGAAAGAGCACACAC-3 and reverse, 5- AGAACTCTACTTCCAGGC-3. PCR reactions were performed in a 12.5 ul final volume containing 16PCR buffer, 1.0 mM Mg2+, 0.2 mM dNTPs, 5 pmol of each primer and 0.3 U Taq polymerase. PCR cycles were the following: 95uC for 5 min followed by 35 cycles each of 95uC for 30 s, 53uC for 30 s, 72uC for 30 s. A final extension step was undertaken at 72uC for 5 min. The 567 base pair sequences of the Bcl-2 gene were amplified by PCR, and their products were digested with restriction endonuclease Ddel (New England BioLabs Inc.). The ancestral allele G yielded three bands of 298, 108 and 161 bp while the mutant allele A yielded two bands of 406 and 161 bp.2.3 MRI AcquisitionAll MR scanning was performed at National Yang-Ming University, Taiwan, using a 3.0 T Siemens MRI scanner with 12 channel head coil (Siemens Magnetom Tim Trio, Erlangen, Germany). High-resol.Is responsible for neuronal aging and degeneration [21]. Increased vulnerability to Bcl-2related apoptosis induced by physiological stressors has been suggested to contribute to the reductions in regional cerebral volumes, neurons, and glial cells in patients with mood disorders [22]. An investigation of the genetic effect of the Bcl-2 rs956572 polymorphism on regional brain-GM volumes in adults aged 19 to 60 years using optimized voxel-based morphometry (VBM) showed that G homozygotes displayed larger GM volumes in the left ventral striatum, compared with that of the A-allele carriers [23]. Recently, we investigated the genetic effects of Bcl-2 rs956572 on regional GM volumes in elderly men [24]. We found that G homozygotes had significantly larger GM volumes in the left precuneus, the right lingual gyrus, and the left superior occipital gyrus, compared with those of the A-allele carriers. Previous studies have reported age-related influences on Bcl-2 expression in specific brain regions [25,26]. Thus, increased vulnerability to Bcl-2-related apoptosis may be involved in the aging process [27]. Considering these findings and the role that Bcl-2 plays in neural plasticity and cellular resilience, we hypothesized that the Bcl-2 rs956572 allelic variant may contribute to age-related changes in GM volumes. Therefore, we evaluated the relationship between the Bcl-2 rs956572 genotype and age-related changes in regional GM volumes based on the results of optimized VBM over a broad age range.including malignancy, heart failure, lung disease, and diabetes; and (6) a Clinical Dementia Rating Scale score over 0.5 for participants aged 65 and over. The cognitive functioning of the participants was evaluated using the MMSE and the Wechsler Digit Span Task tests. All participants had sufficient visual and auditory acuity to undergo cognitive testing. The 30-point MMSE cognitive test was designed for screening cognitive impairment in cross-cultural studies. Our research was conducted in accordance with the Declaration of Helsinki, and was approved by the Institutional Review Board of Taipei Veterans General Hospital. Written, informed consent was 23727046 obtained from all the participants.2.2 GenotypingGenomic DNA was extracted from peripheral blood with a commercial kit (Qiagen, Gentra Puregene Blood Kit). Genotyping procedures for identifying the rs956572 was performed by the polymerase chain reaction (PCR)-restriction fragment length polymorphism method. The following PCR primers, which were synthesized by MISSION BIOTECH Co. (Taiwan) were used in the present study: forward, 5- AGAGGAAAGAGCACACAC-3 and reverse, 5- AGAACTCTACTTCCAGGC-3. PCR reactions were performed in a 12.5 ul final volume containing 16PCR buffer, 1.0 mM Mg2+, 0.2 mM dNTPs, 5 pmol of each primer and 0.3 U Taq polymerase. PCR cycles were the following: 95uC for 5 min followed by 35 cycles each of 95uC for 30 s, 53uC for 30 s, 72uC for 30 s. A final extension step was undertaken at 72uC for 5 min. The 567 base pair sequences of the Bcl-2 gene were amplified by PCR, and their products were digested with restriction endonuclease Ddel (New England BioLabs Inc.). The ancestral allele G yielded three bands of 298, 108 and 161 bp while the mutant allele A yielded two bands of 406 and 161 bp.2.3 MRI AcquisitionAll MR scanning was performed at National Yang-Ming University, Taiwan, using a 3.0 T Siemens MRI scanner with 12 channel head coil (Siemens Magnetom Tim Trio, Erlangen, Germany). High-resol.
