Literature DB >> 31416577

The worldwide mutational landscape of Berardinelli-Seip congenital lipodystrophy.

Aquiles Sales Craveiro Sarmento1, Leonardo Capistrano Ferreira2, Josivan Gomes Lima3, Lázaro Batista de Azevedo Medeiros1, Patrícia Tainá Barbosa Cunha4, Lucymara Fassarella Agnez-Lima1, Marcela Abbott Galvão Ururahy5, Julliane Tamara Araújo de Melo Campos6.   

Abstract

Berardinelli-Seip congenital lipodystrophy (BSCL) is a rare disease characterized by the near total absence of body fat at birth. BSCL etiology involves genetic variations in four different genes: AGPAT2, BSCL2, CAV1, and CAVIN1. The four different biochemical subtypes of the disease are distinguished depending on which gene is mutated. The diagnosis of lipodystrophy can be based on clinical criteria, but the gold standard remains genetic testing. Since many different mutations have already been correlated with the onset of the disease, the most indicative method is DNA sequencing. However, not all laboratories have the resources to perform sequencing. Thus, less expensive techniques that include narrow gene regions may be applied. In such cases, the target mutations to be tested must be carefully determined taking into account the frequency of the description of the mutations in the literature, the nationality of the patient, as well as their phenotype. This review considers the molecular basis of BSCL, including the manual count of the majority of mutations reported in the literature up to the year 2018. Ninety different genetic mutations in 332 cases were reported at different frequencies. Some mutations were distributed homogeneously and others were specific to geographic regions. Type 2 BSCL was mentioned most often in the literature (50.3% of the cases), followed by Type 1 (38.0%), Type 4 (10.2%), and Type 3 (1.5%). The mutations comprised frameshifts (34.4%), nonsense (26.6%), and missense (21.1%). The c.517dupA in the BSCL2 gene was the most frequent (13.3%), followed by c.589-2A>G in the AGPAT2 gene (11.5%), c.507_511delGTATC in the BSCL2 gene (9.7%), c.317-588del in the AGPAT2 gene (7.3%), and c.202C>T in the AGPAT2 gene (4.5%). This information should prove valuable for analysts in making decisions regarding the best therapeutic targets in a population-specific context, which will benefit patients and enable faster and less expensive treatment.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Berardinelli; Caveolin; Lipodystrophy; PTRF; Seipin

Mesh:

Year:  2019        PMID: 31416577     DOI: 10.1016/j.mrrev.2019.03.005

Source DB:  PubMed          Journal:  Mutat Res Rev Mutat Res        ISSN: 1383-5742            Impact factor:   5.657


  8 in total

Review 1.  Role of Seipin in Human Diseases and Experimental Animal Models.

Authors:  Yuying Li; Xinmin Yang; Linrui Peng; Qing Xia; Yuwei Zhang; Wei Huang; Tingting Liu; Da Jia
Journal:  Biomolecules       Date:  2022-06-17

Review 2.  Severe insulin resistance syndromes.

Authors:  Angeliki M Angelidi; Andreas Filippaios; Christos S Mantzoros
Journal:  J Clin Invest       Date:  2021-02-15       Impact factor: 14.808

3.  Altered acylated ghrelin response to food intake in congenital generalized lipodystrophy.

Authors:  Camilla O D Araújo; Renan M Montenegro; Amanda P Pedroso; Virgínia O Fernandes; Ana Paula D R Montenegro; Annelise B de Carvalho; Lila M Oyama; Carla S C Maia; Eliane B Ribeiro
Journal:  PLoS One       Date:  2021-01-07       Impact factor: 3.240

4.  The neonatal onset diabetes mellitus of Chinese neonate with congenital generalized lipodystrophy 2: a case report.

Authors:  Yuan Yang; Li Ma; Jingjing Sun; Xiaohui Gong; Cheng Cai; Wenchao Hong
Journal:  BMC Endocr Disord       Date:  2022-03-29       Impact factor: 2.763

5.  Frataxin controls ketone body metabolism through regulation of OXCT1.

Authors:  Yi Na Dong; Clementina Mesaros; Peining Xu; Elizabeth Mercado-Ayón; Sarah Halawani; Lucie Vanessa Ngaba; Nathan Warren; Patrick Sleiman; Layne N Rodden; Kimberly A Schadt; Ian A Blair; David R Lynch
Journal:  PNAS Nexus       Date:  2022-07-26

6.  Leu124Serfs*26, a novel AGPAT2 mutation in congenital generalized lipodystrophy with early cardiovascular complications.

Authors:  Renan Magalhães Montenegro Junior; Grayce Ellen da Cruz Paiva Lima; Virgínia Oliveira Fernandes; Ana Paula Dias Rangel Montenegro; Clarisse Mourão Melo Ponte; Lívia Vasconcelos Martins; Daniel Pascoalino Pinheiro; Maria Elisabete Amaral de Moraes; Manoel Odorico de Moraes Filho; Catarina Brasil d'Alva
Journal:  Diabetol Metab Syndr       Date:  2020-04-06       Impact factor: 3.320

7.  Congenital Generalized Lipoatrophy (Berardinelli-Seip Syndrome) Type 1: Description of Novel AGPAT2 Homozygous Variants Showing the Highly Heterogeneous Presentation of the Disease.

Authors:  Giovanni Ceccarini; Silvia Magno; Caterina Pelosini; Federica Ferrari; Maria Rita Sessa; Gaia Scabia; Margherita Maffei; Isabelle Jéru; Olivier Lascols; Corinne Vigouroux; Ferruccio Santini
Journal:  Front Endocrinol (Lausanne)       Date:  2020-02-14       Impact factor: 5.555

Review 8.  Seipin Deficiency as a Model of Severe Adipocyte Dysfunction: Lessons from Rodent Models and Teaching for Human Disease.

Authors:  Jocelyne Magré; Xavier Prieur
Journal:  Int J Mol Sci       Date:  2022-01-11       Impact factor: 5.923

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.