Current Status of Familial LCAT Deficiency in Japan

Author:

Kuroda Masayuki1,Bujo Hideaki2,Yokote Koutaro3,Murano Takeyoshi4,Yamaguchi Takashi5,Ogura Masatsune6,Ikewaki Katsunori7,Koseki Masahiro8,Takeuchi Yasuo9,Nakatsuka Atsuko10,Hori Mika11,Matsuki Kota12,Miida Takashi13,Yokoyama Shinji14,Wada Jun10,Harada-Shiba Mariko15,

Affiliation:

1. Center for Advanced Medicine, Chiba University Hospital, Chiba University

2. Department of Clinical-Laboratory and Experimental-Research Medicine, Toho University Sakura Medical Center

3. Department of Endocrinology, Hematology and Gerontology, Chiba University Graduate School of Medicine

4. Clinical Laboratory Program, Faculty of Science, Toho University

5. Center of Diabetes, Endocrinology and Metabolism, Toho University Sakura Medical Center

6. Department of Molecular Innovation in Lipidology, National Cerebral and Cardiovascular Center Research Institute

7. Division of Neurology, Anti-Aging, and Vascular Medicine, Department of Internal Medicine, National Defense Medical College

8. Division of Cardiovascular Medicine, Department of Medicine, Osaka University Graduate School of Medicine

9. Division of Nephrology, Kitasato University School of Medicine

10. Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences

11. Department of Endocrinology, Research Institute of Environmental Medicine, Nagoya University

12. Department of Endocrinology and Metabolism, Hirosaki University Graduate School of Medicine

13. Department of Clinical Laboratory Medicine, Juntendo University Graduate School of Medicine

14. Institute for Biological Functions, Chubu University

15. Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center Research Institute

Publisher

Japan Atherosclerosis Society

Subject

Biochemistry, medical,Cardiology and Cardiovascular Medicine,Internal Medicine

Reference67 articles.

1. 1) Glomset JA, Parker F, Tjaden M, Williams RH. The esterification in vitro of free cholesterol in human and rat plasma. Biochim Biophys Acta, 1962; 58: 398-406

2. 2) Glomset JA, Janssen ET, Kennedy R, Dobbins J. Role of plasma lecithin: cholesterol acyltransferase in the metabolism of high density lipoproteins. J Lipid Res, 1966; 7: 638-648

3. 3) Carlson LA., Philipson B. Fish-eye disease: a new familial condition with massive corneal opacities and dyslipoproteinem. Lancet, 1979; 314: 921-924

4. 4) Glomset JA, Assmann G, Gjone E, Norum KR. Lecithin cholesterol acyltransferase deficiency and fish eye disease. In: The Metabolic and Molecular Bases of Inherited Disease, 7th ed. by Scriver CR, Beaudet AL, Sly WS, Valle D, Stanbury JB, Wyngaarden JB, Fredrickson DS., McGraw-Hill Inc., New York, 1995, 1933-1951

5. 5) Santamarina-Fojo S, Hoeg JM, Assman G, Brewer Jr HB. Lecithin cholesterol acyltransferase deficiency and fish eye disease. In: The metabolic and molecular bases of inherited disease, 8th ed. by Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B., McGraw-Hill Inc., New York, 2001, 2817-2833

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