Abstract | OBJECTIVE: APPROACH AND RESULTS: We used exome sequencing to assess all protein-coding regions of the genome in 3 family members and identified a homozygous exon 8 splice junction mutation (c.894G>A, also known as E8SJM) in LIPA that segregated with the diagnosis of hypercholesterolemia. Because homozygosity for mutations in LIPA is known to cause cholesterol ester storage disease, we performed directed follow-up phenotyping by noninvasively measuring hepatic cholesterol content. We observed abnormal hepatic accumulation of cholesterol in the homozygote individuals, supporting the diagnosis of cholesterol ester storage disease. Given previous suggestions of cardiovascular disease risk in heterozygous LIPA mutation carriers, we genotyped E8SJM in >27 000 individuals and found no association with plasma lipid levels or risk of myocardial infarction, confirming a true recessive mode of inheritance. CONCLUSIONS: By integrating observations from Mendelian and population genetics along with directed clinical phenotyping, we diagnosed clinically unapparent cholesterol ester storage disease in the affected individuals from this kindred and addressed an outstanding question about risk of cardiovascular disease in LIPA E8SJM heterozygous carriers.
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Authors | Nathan O Stitziel, Sigrid W Fouchier, Barbara Sjouke, Gina M Peloso, Alessa M Moscoso, Paul L Auer, Anuj Goel, Bruna Gigante, Timothy A Barnes, Olle Melander, Marju Orho-Melander, Stefano Duga, Suthesh Sivapalaratnam, Majid Nikpay, Nicola Martinelli, Domenico Girelli, Rebecca D Jackson, Charles Kooperberg, Leslie A Lange, Diego Ardissino, Ruth McPherson, Martin Farrall, Hugh Watkins, Muredach P Reilly, Daniel J Rader, Ulf de Faire, Heribert Schunkert, Jeanette Erdmann, Nilesh J Samani, Lawrence Charnas, David Altshuler, Stacey Gabriel, John J P Kastelein, Joep C Defesche, Aart J Nederveen, Sekar Kathiresan, G Kees Hovingh, National Heart, Lung, and Blood Institute GO Exome Sequencing Project |
Journal | Arteriosclerosis, thrombosis, and vascular biology
(Arterioscler Thromb Vasc Biol)
Vol. 33
Issue 12
Pg. 2909-14
(Dec 2013)
ISSN: 1524-4636 [Electronic] United States |
PMID | 24072694
(Publication Type: Journal Article, Meta-Analysis, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Twin Study)
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Chemical References |
- Biomarkers
- Cholesterol, HDL
- Cholesterol, LDL
- Triglycerides
- Cholesterol
- LIPA protein, human
- Sterol Esterase
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Topics |
- Adult
- Biomarkers
(blood)
- Cholesterol
(blood)
- Cholesterol Ester Storage Disease
(blood, diagnosis, genetics)
- Cholesterol, HDL
(blood)
- Cholesterol, LDL
(blood)
- DNA Mutational Analysis
- Exome
- Female
- Genetic Predisposition to Disease
- Genetic Testing
(methods)
- Heredity
- Homozygote
- Humans
- Hypercholesterolemia
(blood, diagnosis, genetics)
- Linear Models
- Liver
(metabolism)
- Male
- Middle Aged
- Mutation
- Pedigree
- Phenotype
- Predictive Value of Tests
- Principal Component Analysis
- Sterol Esterase
(genetics)
- Triglycerides
(blood)
- Young Adult
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