Literature DB >> 22108153

Homozygous lecithin:cholesterol acyltransferase (LCAT) deficiency due to a new loss of function mutation and review of the literature.

Bijan Roshan1, Om P Ganda, Ranil Desilva, Rose B Ganim, Edmund Ward, Sarah D Haessler, Eliana Y Polisecki, Bela F Asztalos, Ernst J Schaefer.   

Abstract

BACKGROUND: A case of homozygous familial lecithin:cholesterol acyltransferase (LCAT) deficiency with a novel homozygous LCAT missense mutation (replacement of methionine by arginine at position 293 in the amino acid sequence of the LCAT protein) is reported. METHODS AND
RESULTS: The probable diagnosis was suggested by findings of marked high density lipoprotein (HDL) deficiency, corneal opacification, anemia, and renal insufficiency. The diagnosis was confirmed by two dimensional gel electrophoresis of HDL, the measurement of free and esterified cholesterol, and sequencing of the LCAT gene.
CONCLUSIONS: In our view the most important aspects of therapy to prevent the kidney disease that these patients develop is careful control of blood pressure and lifestyle measures to optimize non HDL lipoproteins. In the future replacement therapy by gene transfer or other methods may become available.
Copyright © 2011. Published by Elsevier Inc.

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Year:  2011        PMID: 22108153      PMCID: PMC4565181          DOI: 10.1016/j.jacl.2011.07.002

Source DB:  PubMed          Journal:  J Clin Lipidol        ISSN: 1876-4789            Impact factor:   4.766


  30 in total

1.  Resistance to parathyroid hormone in two patients with familial intrahepatic cholestasis: possible involvement of the ATP8B1 gene in calcium regulation via parathyroid hormone.

Authors:  Hironori Nagasaka; Tohru Yorifuji; Kiyotaka Kosugiyama; Hiroto Egawa; Masahiko Kawai; Kei Murayama; Makoto Hasegawa; Ryo Sumazaki; Junko Tsubaki; Hideaki Kikuta; Akira Matsui; Koichi Tanaka; Nobuo Matsuura; Kunihiko Kobayashi
Journal:  J Pediatr Gastroenterol Nutr       Date:  2004-10       Impact factor: 2.839

2.  Splenomegaly with sea-blue histiocytosis, dyslipidemia, and nephropathy in a patient with lecithin-cholesterol acyltransferase deficiency: a clinicopathologic correlation.

Authors:  Mojdeh Naghashpour; Hernani Cualing
Journal:  Metabolism       Date:  2009-07-09       Impact factor: 8.694

3.  Cardiac surgery for a patient with familial lecithin: cholesterol acyltransferase deficiency.

Authors:  Tsukasa Miyatake; Yoshiro Matsui; Makoto Koyama; Toru Watanabe; Satoshi Yamada; Keishu Yasuda
Journal:  Jpn J Thorac Cardiovasc Surg       Date:  2005-06

4.  Lipoprotein-X stimulates monocyte chemoattractant protein-1 expression in mesangial cells via nuclear factor-kappa B.

Authors:  E G Lynn; Y L Siow; J Frohlich; G T Cheung; K O
Journal:  Kidney Int       Date:  2001-08       Impact factor: 10.612

Review 5.  The role of lipids in nephrosclerosis and glomerulosclerosis.

Authors:  E F Gröne; A K Walli; H J Gröne; B Miller; D Seidel
Journal:  Atherosclerosis       Date:  1994-05       Impact factor: 5.162

6.  Lipoprotein abnormalities in primary biliary cirrhosis. Association with hepatic lipase inhibition as well as altered cholesterol esterification.

Authors:  C E Jahn; E J Schaefer; L A Taam; J H Hoofnagle; F T Lindgren; J J Albers; E A Jones; H B Brewer
Journal:  Gastroenterology       Date:  1985-12       Impact factor: 22.682

7.  Possible induction of renal dysfunction in patients with lecithin:cholesterol acyltransferase deficiency by oxidized phosphatidylcholine in glomeruli.

Authors:  S Jimi; N Uesugi; K Saku; H Itabe; B Zhang; K Arakawa; S Takebayashi
Journal:  Arterioscler Thromb Vasc Biol       Date:  1999-03       Impact factor: 8.311

8.  Familial combined hyperlipidemia is associated with alterations in the cholesterol synthesis pathway.

Authors:  Thomas M van Himbergen; Seiko Otokozawa; Nirupa R Matthan; Ernst J Schaefer; Aaron Buchsbaum; Masumi Ai; Lambertus J H van Tits; Jacqueline de Graaf; Anton F H Stalenhoef
Journal:  Arterioscler Thromb Vasc Biol       Date:  2009-10-15       Impact factor: 8.311

9.  Lipoprotein-X reduces LDL atherogenicity in primary biliary cirrhosis by preventing LDL oxidation.

Authors:  Po-Yuan Chang; Shao-Chun Lu; Ta-Chen Su; San-Fang Chou; Wen-Huei Huang; Joel D Morrisett; Chu-Huang Chen; Chiau-Suong Liau; Yuan-Teh Lee
Journal:  J Lipid Res       Date:  2004-08-16       Impact factor: 5.922

10.  In vivo imaging of the cornea in a patient with lecithin-cholesterol acyltransferase deficiency.

Authors:  Pat-Michael Palmiero; Zaher Sbeity; Jeffrey Liebmann; Robert Ritch
Journal:  Cornea       Date:  2009-10       Impact factor: 2.651

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  9 in total

Review 1.  HDL and atherosclerotic cardiovascular disease: genetic insights into complex biology.

Authors:  Robert S Rosenson; H Bryan Brewer; Philip J Barter; Johan L M Björkegren; M John Chapman; Daniel Gaudet; Daniel Seung Kim; Eric Niesor; Kerry-Anne Rye; Frank M Sacks; Jean-Claude Tardif; Robert A Hegele
Journal:  Nat Rev Cardiol       Date:  2017-08-10       Impact factor: 32.419

2.  Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement.

Authors:  Robert D Shamburek; Rebecca Bakker-Arkema; Bruce J Auerbach; Brian R Krause; Reynold Homan; Marcelo J Amar; Lita A Freeman; Alan T Remaley
Journal:  J Clin Lipidol       Date:  2015-12-23       Impact factor: 4.766

Review 3.  Diagnosis and treatment of high density lipoprotein deficiency.

Authors:  Ernst J Schaefer; Pimjai Anthanont; Margaret R Diffenderfer; Eliana Polisecki; Bela F Asztalos
Journal:  Prog Cardiovasc Dis       Date:  2016-08-24       Impact factor: 8.194

4.  A Systematic Investigation of Structure/Function Requirements for the Apolipoprotein A-I/Lecithin Cholesterol Acyltransferase Interaction Loop of High-density Lipoprotein.

Authors:  Xiaodong Gu; Zhiping Wu; Ying Huang; Matthew A Wagner; Camelia Baleanu-Gogonea; Ryan A Mehl; Jennifer A Buffa; Anthony J DiDonato; Leah B Hazen; Paul L Fox; Valentin Gogonea; John S Parks; Joseph A DiDonato; Stanley L Hazen
Journal:  J Biol Chem       Date:  2016-01-21       Impact factor: 5.157

5.  Genetic and secondary causes of severe HDL deficiency and cardiovascular disease.

Authors:  Andrew S Geller; Eliana Y Polisecki; Margaret R Diffenderfer; Bela F Asztalos; Sotirios K Karathanasis; Robert A Hegele; Ernst J Schaefer
Journal:  J Lipid Res       Date:  2018-10-17       Impact factor: 5.922

6.  Selective Correction of Genotype Yield by Probucol in HDL-Deficient Mice Propagation.

Authors:  Maki Tsujita; Nobukatsu Akita; Tomo Yokota; Fumihiko Kobayashi; Shinji Yokoyama
Journal:  J Atheroscler Thromb       Date:  2019-05-14       Impact factor: 4.928

Review 7.  Structural Insights into High Density Lipoprotein: Old Models and New Facts.

Authors:  Valentin Gogonea
Journal:  Front Pharmacol       Date:  2016-01-12       Impact factor: 5.810

Review 8.  A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency.

Authors:  Cecilia Vitali; Archna Bajaj; Christina Nguyen; Jill Schnall; Jinbo Chen; Kostas Stylianou; Daniel J Rader; Marina Cuchel
Journal:  J Lipid Res       Date:  2022-01-20       Impact factor: 5.922

9.  LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred.

Authors:  Roopa Mehta; Daniel Elías-López; Alexandro J Martagón; Oscar A Pérez-Méndez; Maria Luisa Ordóñez Sánchez; Yayoi Segura; Maria Teresa Tusié; Carlos A Aguilar-Salinas
Journal:  Lipids Health Dis       Date:  2021-07-13       Impact factor: 3.876

  9 in total

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