TY - JOUR
T1 - High frequency of type 2 diabetes and impaired glucose tolerance in Japanese subjects with the angiopoietin-like protein 8 R59W variant
AU - Liu, Jianhui
AU - Yagi, Kunimasa
AU - Nohara, Atsushi
AU - Chujo, Daisuke
AU - Ohbatake, Azusa
AU - Fujimoto, Aya
AU - Miyamoto, Yukiko
AU - Kobayashi, Junji
AU - Yamagishi, Masakazu
N1 - Publisher Copyright:
© 2017 National Lipid Association
PY - 2018/3/1
Y1 - 2018/3/1
N2 - Background: Angiopoietin-like protein 8 (ANGPTL8) is considered to be metabolically multifunctional. One notable function still to be elucidated definitively is a betatrophic role in protecting and preserving pancreatic beta-cell function. There is, however, a paucity of data regarding the role of ANGPTL8 in the etiology of type 2 diabetes (T2D), but some findings of human research have suggested the potential for significant involvement. Objective: To examine the frequency of T2D and impaired glucose tolerance (IGT) in Japanese subjects with the ANGPTL8 R59W variant. Methods: ANGPTL8 R59W (Rs2278426, c.194C > T) was determined by polymerase chain reaction–restriction fragment length polymorphism using the restriction enzyme FokI in 797 consecutive Japanese individuals. Subjects with triglyceride levels greater than or equal to 150 mg/dL were considered to be hypertriglyceridemic. Results: Genotype frequencies of ANGPTL8 R59W were as follows: wild-type RR (C/C) 53.5%, RW (C/T) 36.6%, and WW (T/T) 9.9%. T2D and IGT were significantly prevalent in WW and RW subjects relative to RR among all 797 subjects (P =.0138) and also in hypertriglyceridemic subjects (P =.0015). In multiple logistic regression models for the existence of T2D and IGT in hypertriglyceridemic subjects, the odds ratio for heterozygote RW and homozygote WW genotypes to wild-type RR was 2.406 (P =.0017) after controlling the risk factors of age, gender, and body mass index as covariates. Conclusions: The frequency of ANGPTL8 R59W is significantly higher in Japanese subjects than in other ethnic groups. The rates of T2D and IGT were greater in subjects with the R59W variant. These findings indicate that ANGPTL8 is a participant in diabetes and a potential therapeutic target for T2D prevention, especially in East Asians.
AB - Background: Angiopoietin-like protein 8 (ANGPTL8) is considered to be metabolically multifunctional. One notable function still to be elucidated definitively is a betatrophic role in protecting and preserving pancreatic beta-cell function. There is, however, a paucity of data regarding the role of ANGPTL8 in the etiology of type 2 diabetes (T2D), but some findings of human research have suggested the potential for significant involvement. Objective: To examine the frequency of T2D and impaired glucose tolerance (IGT) in Japanese subjects with the ANGPTL8 R59W variant. Methods: ANGPTL8 R59W (Rs2278426, c.194C > T) was determined by polymerase chain reaction–restriction fragment length polymorphism using the restriction enzyme FokI in 797 consecutive Japanese individuals. Subjects with triglyceride levels greater than or equal to 150 mg/dL were considered to be hypertriglyceridemic. Results: Genotype frequencies of ANGPTL8 R59W were as follows: wild-type RR (C/C) 53.5%, RW (C/T) 36.6%, and WW (T/T) 9.9%. T2D and IGT were significantly prevalent in WW and RW subjects relative to RR among all 797 subjects (P =.0138) and also in hypertriglyceridemic subjects (P =.0015). In multiple logistic regression models for the existence of T2D and IGT in hypertriglyceridemic subjects, the odds ratio for heterozygote RW and homozygote WW genotypes to wild-type RR was 2.406 (P =.0017) after controlling the risk factors of age, gender, and body mass index as covariates. Conclusions: The frequency of ANGPTL8 R59W is significantly higher in Japanese subjects than in other ethnic groups. The rates of T2D and IGT were greater in subjects with the R59W variant. These findings indicate that ANGPTL8 is a participant in diabetes and a potential therapeutic target for T2D prevention, especially in East Asians.
KW - Angiopoietin-like protein 8
KW - Betatrophin
KW - Diabetes
KW - Hyperlipidemia
KW - Hypertriglyceridemia
UR - http://www.scopus.com/inward/record.url?scp=85041317205&partnerID=8YFLogxK
U2 - 10.1016/j.jacl.2017.12.011
DO - 10.1016/j.jacl.2017.12.011
M3 - 学術論文
C2 - 29397342
AN - SCOPUS:85041317205
SN - 1933-2874
VL - 12
SP - 331
EP - 337
JO - Journal of Clinical Lipidology
JF - Journal of Clinical Lipidology
IS - 2
ER -