Impaired insulin secretion in four tangier disease patients with ABCA1 mutations

Masahiro Koseki, Akifumi Matsuyama, Kazuhiro Nakatani, Miwako Inagaki, Hajime Nakaoka, Ryota Kawase, Miyako Yuasa-Kawase, Kazumi Tsubakio-Yamamoto, Daisaku Masuda, Jose C. Sandoval, Tohru Ohama, Yumiko Nakagawa-Toyama, Fumihiko Matsuura, Makoto Nishida, Masato Ishigami, Ken Ichi Hirano, Naoki Sakane, Yoshitaka Kumon, Tadashi Suehiro, Tadashi NakamuraIichiro Shimomura, Shizuya Yamashita

研究成果: Article査読

54 被引用数 (Scopus)


Aim: Tangier disease (TD), caused by deficiency of ATP-binding cassette transporter A1, is characterized by the absence of high density lipoprotein and the accumulation of cholesteryl esters in many tissues. Recently, it has been reported that ABCA1 is expressed in pancreatic β cells and mice with specific inactivation of ABCA1 in β cells showed markedly impaired insulin secretion, suggesting that ABCA1 deficiency may be involved in diabetes. The aim of the current study was to confirm these findings by the oral glucose tolerance test (OGTT) in human subjects with ABCA1 deficiency. Methods and Results: Four Japanese patients with TD were investigated by OGTT with 75 g glucose. In all TD patients, the plasma glucose concentration after 30 min progressively increased, indicating a type 2 diabetic pattern; however the plasma insulin concentration did not respond well to glucose increase. The calculated insulinogenic index was significantly lower in TD patients than in non-diabetic controls (0.055±0.034 vs 0.775±0.538, mean±SD, p<0.05, respectively). Conclusions: Although the number of TD patients was very small in the current study, these observations indicated a possible mechanism that glucose-stimulated insulin secretion might be impaired in human TD patients with ABCA1 mutations. Taken together, ABCA1 may be involved in insulin secretion from pancreatic β-cells.

ジャーナルJournal of atherosclerosis and thrombosis
出版ステータスPublished - 2009

All Science Journal Classification (ASJC) codes

  • 内科学
  • 循環器および心血管医学
  • 生化学、医学


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