Literature DB >> 18559913

A new PCSK9 gene promoter variant affects gene expression and causes autosomal dominant hypercholesterolemia.

Sebastian Blesa1, Santiago Vernia, Ana-Barbara Garcia-Garcia, Sergio Martinez-Hervas, Carmen Ivorra, Veronica Gonzalez-Albert, Juan Francisco Ascaso, Juan Carlos Martín-Escudero, Jose Tomas Real, Rafael Carmena, Marta Casado, Felipe Javier Chaves.   

Abstract

CONTEXT: Autosomal dominant hypercholesterolemia (ADH) is a genetic disorder characterized by increased low-density lipoprotein (LDL)-cholesterol levels, leading to high risk of premature cardiovascular disease. More than 900 mutations in LDL receptor, six in APOB and 10 in PCSK9 have been identified as a cause of the disease in different populations. All known mutations in PCSK9 causing hypercholesterolemia produce an increase in the enzymatic activity of this protease. Up to now, there are data about the implication of PCSK9 in ADH in a low number of populations, not including a Spanish population.
OBJECTIVE: The objective of the study was to study the prevalence of PCSK9 mutations in ADH Spanish population. PARTICIPANTS: We screened PCSK9 gene in 42 independent ADH patients in whom mutations in LDL receptor and APOB genes had been excluded.
RESULTS: None of the known mutations causing ADH was detected in our sample, but we found two variations in the promoter region that could cause ADH, c.-288G>A and c.-332C>A (each in one proband). The analysis of the effect of these two variations on the transcription activity of the PCSK9 promoter showed that c.-288G>A did not modify the transcription, whereas c.-332C>A variant caused a 2.5-fold increase when compared with the wild-type sequence, either with or without lovastatin.
CONCLUSIONS: PCSK9 is a rare cause of ADH in Spanish population and, up to what we know, none of the previously described mutations has been detected. We have identified a new mutation that could cause ADH by increasing the transcription of PCSK9.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18559913     DOI: 10.1210/jc.2008-0269

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  5 in total

1.  A Very Rare Variant in SREBF2, a Possible Cause of Hypercholesterolemia and Increased Glycemic Levels.

Authors:  Ana-Bárbara García-García; Sergio Martínez-Hervás; Santiago Vernia; Carmen Ivorra; Inés Pulido; Juan-Carlos Martín-Escudero; Marta Casado; Julián Carretero; José T Real; Felipe Javier Chaves
Journal:  Biomedicines       Date:  2022-05-19

2.  Use of PCSK9 Inhibitor in a Mexican Boy with Compound Heterozygous Familial Hypercholesterolemia: A Case Report.

Authors:  José Juan Ceballos-Macías; Ramón Madriz-Prado; Norma Alejandra Vázquez Cárdenas; Carlos Aguilar-Salinas; Maria Teresa Tusié-Luna; Jorge Alberto Flores-Real; Guillermo Ortega-Gutiérrez; Joel Vargas-Sánchez; Carolina Lara-Sánchez; Alfredo Hernández-Moreno
Journal:  J Endocr Soc       Date:  2019-11-21

Review 3.  PCSK9 Variants in Familial Hypercholesterolemia: A Comprehensive Synopsis.

Authors:  Qianyun Guo; Xunxun Feng; Yujie Zhou
Journal:  Front Genet       Date:  2020-09-23       Impact factor: 4.599

4.  The Role of Registers in Increasing Knowledge and Improving Management of Children and Adolescents Affected by Familial Hypercholesterolemia: the LIPIGEN Pediatric Group.

Authors:  Marta Gazzotti; Manuela Casula; Stefano Bertolini; Maria Elena Capra; Elena Olmastroni; Alberico Luigi Catapano; Cristina Pederiva
Journal:  Front Genet       Date:  2022-06-20       Impact factor: 4.772

Review 5.  Proprotein convertase subtilisin/kexin type 9: from the discovery to the development of new therapies for cardiovascular diseases.

Authors:  Nicola Ferri
Journal:  Scientifica (Cairo)       Date:  2012-09-11
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.