Familial hypobetalipoproteinemia: analysis of three Spanish cases with two new mutations in the APOB gene.

Abstract

Extremely low LDL-cholesterol concentrations are very unusual and generally related with comorbidities accompanying malnutrition. Less frequently low LDL-cholesterol levels result from mutations in the APOB, PCSK9, ANGPTL3, SAR1B and MTTP genes (primary hypobetalipoproteinemia). We investigated three patients with plasma LDL-cholesterol levels below the fifth percentile of the Spanish population. We recorded data on demographic and anthropometric characteristics, life style habits, physical examination, liver ultrasound and lipid and lipoprotein levels, in the probands and their first-degree relatives. Secondary causes of hypocholesterolemia were ruled out by clinical study, complementary tests and follow-up. The APOB, MTTP and SAR1B genes were sequenced. Patients were found to be heterozygotes for point mutations located in the exon 26 of the APOB gene. One patient, with fatty liver, carried a previously described mutation (c.7600C>T) (Arg2507X), causing the formation of truncated Apo B-55.25. The other two mutations producing truncations are new. One asymptomatic patient carried the Arg3672X (Apo B-80.93) and the other with fatty liver and steatorrhea carried the Ser2184fsVal2193X (Apo B-48.32). Our study reinforces the concept that in the heterozygous carriers of truncated Apo Bs, the clinical manifestations of FHBL are dependent on the size of the truncations.

• Authors: R Martín-Morales, J D García-Díaz, P Tarugi, P González-Santos, P Saavedra-Vallejo, L Magnolo, J M Mesa-Latorre, E di Leo, P Valdivielso
• Journal: Gene (Gene) Vol. 531 Issue 1 Pg. 92-6 (Nov 15 2013) ISSN: 1879-0038 [Electronic] Netherlands
• PMID: 24001780 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2013 Elsevier B.V. All rights reserved.

Chemical References

• Apolipoproteins B

Topics

• Adult
• Aged
• Apolipoproteins B (blood, genetics)
• Female
• Heterozygote
• Humans
• Hypobetalipoproteinemias (diagnosis, genetics)
• Intestinal Mucosa (metabolism)
• Intestines (pathology)
• Male
• Mutation
• Spain
• White People
• Young Adult