TY - JOUR
T1 - Alcohol drinking and brain morphometry in apparently healthy community-dwelling Japanese men
AU - for the SESSA Research Group
AU - Co-chairpersons
AU - Research members
AU - Syaifullah, Ali Haidar
AU - Shiino, Akihiko
AU - Fujiyoshi, Akira
AU - Kadota, Aya
AU - Kondo, Keiko
AU - Ito, Takahiro
AU - Segawa, Hiroyoshi
AU - Moniruzzaman, Mohammad
AU - Waki, Takashi
AU - Miyagawa, Naoko
AU - Tooyama, Ikuo
AU - Ueshima, Hirotsugu
AU - Miura, Katsuyuki
AU - Horie, Minoru
AU - Nakagawa, Yoshihisa
AU - Yamamoto, Takashi
AU - Nakano, Yasutaka
AU - Ogawa, Emiko
AU - Maegawa, Hiroshi
AU - Morino, Katsutaro
AU - Miyazawa, Itsuko
AU - Watanabe, Yoshiyuki
AU - Nozaki, Kazuhiko
AU - Andoh, Akira
AU - Tsuru, Teruhiko
AU - Ogita, Hisakazu
AU - Miyamatsu, Naomi
AU - Nakamura, Yasuyuki
AU - Torii, Sayuki
AU - Kadowaki, Takashi
AU - Kadowaki, Sayaka
AU - Suzuki, Sentaro
AU - Kunimura, Ayako
AU - Higashiyama, Aya
AU - Okamura, Tomonori
AU - Azuma, Koichiro
AU - Sawamura, Tatsuya
AU - Igase, Michiya
AU - Tabara, Yasuharu
AU - Sekikawa, Akira
AU - Barinas-Mitchell, Emma J.M.
AU - Edmundowicz, Daniel
AU - Ohkubo, Takayoshi
AU - Hozawa, Atsushi
AU - Murakami, Yoshitaka
AU - Okuda, Nagako
AU - Arima, Hisatomi
AU - Satoh, Atsushi
AU - Kita, Yoshikuni
AU - Hisamatsu, Takashi
N1 - Funding Information:
We would like to thank the staff, investigators, and participants of Shiga Epidemiological Study of Subclinical Atherosclerosis (SESSA) for their commitment and dedication. SESSA is supported by Grants-in-Aid for Scientific Research (A) 13307016 , (A) 17209023 , (A) 21249043 , (A) 23249036 , (A) 25253046 , (A) 15H02528 , (A) 18H04074 , (B) 26293140 , (B) 24790616 , (B) 21790579 , and (B) 18H03048 from the Ministry of Education, Culture, Sports, Science and Technology of Japan and by Grant R01HL068200 from GlaxoSmithKline GB. This study was initiated and analyzed by the authors. The funding sources listed above had no impact on the design, collection, analysis, and interpretation of the work.
Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2021/2
Y1 - 2021/2
N2 - The clinical implications of alcohol consumption have been extensively examined; however, its effects on brain structures in apparently healthy community-dwellers remain unclear. Therefore, we investigated the relationship between alcohol consumption and brain gray matter volume (GMV) in community-dwelling Japanese men using voxel-based morphometry (VBM). We recruited cognitively intact Japanese men, aged 40–79 years, from a population-based cohort in Shiga, Japan. Brain magnetic resonance imaging was performed, on average, 2 years after demographic and medical information was obtained in 2010–2014. A multivariable linear regression analysis of 639 men was conducted to elucidate the relationship between the amount of alcohol consumed and GMV. VBM statistics were analyzed by threshold-free cluster enhancement with a family-wise error rate of <0.05. The results obtained demonstrated that the amount of alcohol consumed was associated with lower GMV. The VBM analysis showed lower GMV within the parahippocampal, entorhinal, cingulate, insular, temporal, and frontal cortices and cerebellum in very heavy drinkers (≥42 ethanol g/day) than in non-drinkers. Furthermore, alcohol consumption was associated with a higher white matter lesion volume. These results suggest subclinical structural changes similar to alcohol-related neurological diseases.
AB - The clinical implications of alcohol consumption have been extensively examined; however, its effects on brain structures in apparently healthy community-dwellers remain unclear. Therefore, we investigated the relationship between alcohol consumption and brain gray matter volume (GMV) in community-dwelling Japanese men using voxel-based morphometry (VBM). We recruited cognitively intact Japanese men, aged 40–79 years, from a population-based cohort in Shiga, Japan. Brain magnetic resonance imaging was performed, on average, 2 years after demographic and medical information was obtained in 2010–2014. A multivariable linear regression analysis of 639 men was conducted to elucidate the relationship between the amount of alcohol consumed and GMV. VBM statistics were analyzed by threshold-free cluster enhancement with a family-wise error rate of <0.05. The results obtained demonstrated that the amount of alcohol consumed was associated with lower GMV. The VBM analysis showed lower GMV within the parahippocampal, entorhinal, cingulate, insular, temporal, and frontal cortices and cerebellum in very heavy drinkers (≥42 ethanol g/day) than in non-drinkers. Furthermore, alcohol consumption was associated with a higher white matter lesion volume. These results suggest subclinical structural changes similar to alcohol-related neurological diseases.
KW - alcohol consumption
KW - brain atrophy
KW - japanese population
KW - neuroimaging
KW - voxel-based morphometry
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U2 - 10.1016/j.alcohol.2020.11.006
DO - 10.1016/j.alcohol.2020.11.006
M3 - Article
C2 - 33278513
AN - SCOPUS:85099179437
SN - 0741-8329
VL - 90
SP - 57
EP - 65
JO - Alcohol
JF - Alcohol
ER -