Literature DB >> 28476236

Genetics of Lipodystrophy.

Marissa Lightbourne1, Rebecca J Brown2.   

Abstract

Lipodystrophy disorders are characterized by selective loss of fat tissue with metabolic complications including insulin resistance, hypertriglyceridemia, and nonalcoholic liver disease. These complications can be life-threatening, affect quality of life, and result in increased health care costs. Genetic discoveries have been particularly helpful in understanding the pathophysiology of these diseases, and have shown that mutations affect pathways involved in adipocyte differentiation and survival, lipid droplet formation, and lipid synthesis. In addition, genetic testing can identify patients whose phenotypes are not clearly apparent, but who may still be affected by severe metabolic complications. Published by Elsevier Inc.

Entities:  

Keywords:  Berardinelli-Seip syndrome; Dunnigan syndrome; Kobberling syndrome; Leptin; Lipodystrophy

Mesh:

Year:  2017        PMID: 28476236      PMCID: PMC5424609          DOI: 10.1016/j.ecl.2017.01.012

Source DB:  PubMed          Journal:  Endocrinol Metab Clin North Am        ISSN: 0889-8529            Impact factor:   4.741


  69 in total

1.  Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy.

Authors:  H Cao; R A Hegele
Journal:  Hum Mol Genet       Date:  2000-01-01       Impact factor: 6.150

2.  Lamin a truncation in Hutchinson-Gilford progeria.

Authors:  Annachiara De Sandre-Giovannoli; Rafaëlle Bernard; Pierre Cau; Claire Navarro; Jeanne Amiel; Irène Boccaccio; Stanislas Lyonnet; Colin L Stewart; Arnold Munnich; Martine Le Merrer; Nicolas Lévy
Journal:  Science       Date:  2003-04-17       Impact factor: 47.728

3.  LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

Authors:  S Shackleton; D J Lloyd; S N Jackson; R Evans; M F Niermeijer; B M Singh; H Schmidt; G Brabant; S Kumar; P N Durrington; S Gregory; S O'Rahilly; R C Trembath
Journal:  Nat Genet       Date:  2000-02       Impact factor: 38.330

4.  Cardiomyopathy in congenital complete lipodystrophy.

Authors:  S Bhayana; V M Siu; G I Joubert; C L Clarson; H Cao; R A Hegele
Journal:  Clin Genet       Date:  2002-04       Impact factor: 4.438

5.  PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome.

Authors:  Anil K Agarwal; Chao Xing; George N DeMartino; Dario Mizrachi; Maria Dolores Hernandez; Ana Berta Sousa; Laura Martínez de Villarreal; Heloísa G dos Santos; Abhimanyu Garg
Journal:  Am J Hum Genet       Date:  2010-12-10       Impact factor: 11.025

6.  Premature atherosclerosis associated with monogenic insulin resistance.

Authors:  R A Hegele
Journal:  Circulation       Date:  2001-05-08       Impact factor: 29.690

7.  The lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology.

Authors:  Kimberly M Szymanski; Derk Binns; René Bartz; Nick V Grishin; Wei-Ping Li; Anil K Agarwal; Abhimanyu Garg; Richard G W Anderson; Joel M Goodman
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-18       Impact factor: 11.205

8.  Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy.

Authors:  C A Kim; Marc Delépine; Emilie Boutet; Haquima El Mourabit; Soazig Le Lay; Muriel Meier; Mona Nemani; Etienne Bridel; Claudia C Leite; Debora R Bertola; Robert K Semple; Stephen O'Rahilly; Isabelle Dugail; Jacqueline Capeau; Mark Lathrop; Jocelyne Magré
Journal:  J Clin Endocrinol Metab       Date:  2008-01-22       Impact factor: 5.958

9.  Increased skeletal muscle volume in women with familial partial lipodystrophy, Dunnigan variety.

Authors:  Hongzhao Ji; Paul Weatherall; Beverley Adams-Huet; Abhimanyu Garg
Journal:  J Clin Endocrinol Metab       Date:  2013-06-19       Impact factor: 5.958

10.  Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features.

Authors:  Davor Lessel; Bruno Vaz; Swagata Halder; Paul J Lockhart; Ivana Marinovic-Terzic; Jaime Lopez-Mosqueda; Melanie Philipp; Joe C H Sim; Katherine R Smith; Judith Oehler; Elisa Cabrera; Raimundo Freire; Kate Pope; Amsha Nahid; Fiona Norris; Richard J Leventer; Martin B Delatycki; Gotthold Barbi; Simon von Ameln; Josef Högel; Marina Degoricija; Regina Fertig; Martin D Burkhalter; Kay Hofmann; Holger Thiele; Janine Altmüller; Gudrun Nürnberg; Peter Nürnberg; Melanie Bahlo; George M Martin; Cora M Aalfs; Junko Oshima; Janos Terzic; David J Amor; Ivan Dikic; Kristijan Ramadan; Christian Kubisch
Journal:  Nat Genet       Date:  2014-09-28       Impact factor: 38.330

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  12 in total

1.  Multiple sites acquired lipodystrophy in two siblings: a rare adverse effect of intramuscular triamcinolone.

Authors:  Indar Kumar Sharawat; Jaivinder Yadav; Lesa Dawman
Journal:  BMJ Case Rep       Date:  2019-06-25

2.  From GWAS Association to Function: Candidate Gene Screening Within Insulin Resistance-Associated Genomic Loci Using a Preadipocyte Differentiation Model.

Authors:  Feria A Ladha; Michael L Stitzel; J Travis Hinson
Journal:  Circ Res       Date:  2020-01-30       Impact factor: 17.367

3.  Looking for the skeleton in the closet-rare genetic diagnoses in patients with diabetes and skeletal manifestations.

Authors:  Avivit Brener; Leonid Zeitlin; Yael Wilnai; Ohad S Birk; Talya Rosenfeld; Efrat Chorna; Yael Lebenthal
Journal:  Acta Diabetol       Date:  2022-02-08       Impact factor: 4.280

Review 4.  Neuroanatomical Framework of the Metabolic Control of Reproduction.

Authors:  Jennifer W Hill; Carol F Elias
Journal:  Physiol Rev       Date:  2018-10-01       Impact factor: 37.312

5.  A Single Complex Agpat2 Allele in a Patient With Partial Lipodystrophy.

Authors:  Marjoleine F Broekema; Maarten P G Massink; Joep De Ligt; Edwin C A Stigter; Houshang Monajemi; Jeroen De Ridder; Boudewijn M T Burgering; Gijs W van Haaften; Eric Kalkhoven
Journal:  Front Physiol       Date:  2018-09-26       Impact factor: 4.566

Review 6.  Current Diagnosis, Treatment and Clinical Challenges in the Management of Lipodystrophy Syndromes in Children and Young People

Authors:  Samim Özen; Barış Akıncı; Elif A. Oral
Journal:  J Clin Res Pediatr Endocrinol       Date:  2019-08-22

Review 7.  Caveolae and Lipid Rafts in Endothelium: Valuable Organelles for Multiple Functions.

Authors:  Antonio Filippini; Alessio D'Alessio
Journal:  Biomolecules       Date:  2020-08-21

8.  RNA-seq of peripheral blood mononuclear cells of congenital generalized lipodystrophy type 2 patients.

Authors:  Yen-Hua Huang; Tzu-Chien Su; Chung-Hsing Wang; Siew-Lee Wong; Yin-Hsiu Chien; Yu-Tai Wang; Wuh-Liang Hwu; Ni-Chung Lee
Journal:  Sci Data       Date:  2021-10-13       Impact factor: 6.444

9.  A Multi-Gene Panel to Identify Lipedema-Predisposing Genetic Variants by a Next-Generation Sequencing Strategy.

Authors:  Sandro Michelini; Karen L Herbst; Vincenza Precone; Elena Manara; Giuseppe Marceddu; Astrit Dautaj; Paolo Enrico Maltese; Stefano Paolacci; Maria Rachele Ceccarini; Tommaso Beccari; Elisa Sorrentino; Barbara Aquilanti; Valeria Velluti; Giuseppina Matera; Lucilla Gagliardi; Giacinto Abele Donato Miggiano; Matteo Bertelli
Journal:  J Pers Med       Date:  2022-02-11

10.  Mediation role of body fat distribution (FD) on the relationship between CAV1 rs3807992 polymorphism and metabolic syndrome in overweight and obese women.

Authors:  Faezeh Abaj; Said Abdul Ghafour Saeedy; Khadijeh Mirzaei
Journal:  BMC Med Genomics       Date:  2021-08-12       Impact factor: 3.063

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