Literature DB >> 33994405

Current Diagnosis and Management of Abetalipoproteinemia.

Manabu Takahashi1, Hiroaki Okazaki2, Ken Ohashi3, Masatsune Ogura4, Shun Ishibashi5, Sachiko Okazaki6, Satoshi Hirayama7, Mika Hori8, Kota Matsuki9, Shinji Yokoyama10, Mariko Harada-Shiba11.   

Abstract

Abetalipoproteinemia (ABL) is a rare autosomal recessive disorder caused by biallelic pathogenic mutations in the MTTP gene. Deficiency of microsomal triglyceride transfer protein (MTTP) abrogates the assembly of apolipoprotein (apo) B-containing lipoprotein in the intestine and liver, resulting in malabsorption of fat and fat-soluble vitamins and severe hypolipidemia. Patients with ABL typically manifest steatorrhea, vomiting, and failure to thrive in infancy. The deficiency of fat-soluble vitamins progressively develops into a variety of symptoms later in life, including hematological (acanthocytosis, anemia, bleeding tendency, etc.), neuromuscular (spinocerebellar ataxia, peripheral neuropathy, myopathy, etc.), and ophthalmological symptoms (e.g., retinitis pigmentosa). If left untreated, the disease can be debilitating and even lethal by the third decade of life due to the development of severe complications, such as blindness, neuromyopathy, and respiratory failure. High dose vitamin supplementation is the mainstay for treatment and may prevent, delay, or alleviate the complications and improve the prognosis, enabling some patients to live to the eighth decade of life. However, it cannot fully prevent or restore impaired function. Novel therapeutic modalities that improve quality of life and prognosis are awaited. The aim of this review is to 1) summarize the pathogenesis, clinical signs and symptoms, diagnosis, and management of ABL, and 2) propose diagnostic criteria that define eligibility to receive financial support from the Japanese government for patients with ABL as a rare and intractable disease. In addition, our diagnostic criteria and the entry criterion of low-density lipoprotein cholesterol (LDL-C) <15 mg/dL and apoB <15 mg/dL can be useful in universal or opportunistic screening for the disease. Registry research on ABL is currently ongoing to better understand the disease burden and unmet needs of this life-threatening disease with few therapeutic options.

Entities:  

Keywords:  Abetalipoproteinemia; Chylomicron; Fat-soluble vitamin; Hypolipidemia; MTTP; VLDL

Mesh:

Substances:

Year:  2021        PMID: 33994405      PMCID: PMC8560840          DOI: 10.5551/jat.RV17056

Source DB:  PubMed          Journal:  J Atheroscler Thromb        ISSN: 1340-3478            Impact factor:   4.928


  48 in total

1.  Malformation of the erythrocytes in a case of atypical retinitis pigmentosa.

Authors:  F A BASSEN; A L KORNZWEIG
Journal:  Blood       Date:  1950-04       Impact factor: 22.113

2.  Clinical utility gene card for: Familial hypobetalipoproteinaemia (APOB)--Update 2014.

Authors:  John R Burnett; Damon A Bell; Amanda J Hooper; Robert A Hegele
Journal:  Eur J Hum Genet       Date:  2014-10-22       Impact factor: 4.246

3.  Two infants with abetalipoproteinemia: Classic versus atypical presentation.

Authors:  Noparat Prachasitthisak; Pornthep Tanpowpong; Thipwimol Tim-Aroon; Suporn Treepongkaruna; Nalinee Chongviriyaphan; Niyada Vithayasai; Orawan Iamopas; Duangrurdee Wattanasirichaigoon
Journal:  Pediatr Int       Date:  2019-05-14       Impact factor: 1.524

4.  A mild case of abetalipoproteinaemia in association with subclinical hypothyroidism.

Authors:  Huda A Al-Mahdili; Amanda J Hooper; David R Sullivan; Peter M Stewart; John R Burnett
Journal:  Ann Clin Biochem       Date:  2006-11       Impact factor: 2.057

5.  Identification of a novel mutation of MTP gene in a patient with abetalipoproteinemia.

Authors:  Mehri Najafi Sani; Mozhgan Sabbaghian; Fatemeh Mahjoob; Angelo B Cefalù; Maurizio R Averna; Nima Rezaei
Journal:  Ann Hepatol       Date:  2011 Apr-Jun       Impact factor: 2.400

6.  Normal serum ApoB48 and red cells vitamin E concentrations after supplementation in a novel compound heterozygous case of abetalipoproteinemia.

Authors:  Mathilde Di Filippo; Sophie Collardeau Frachon; Alexandre Janin; Sujith Rajan; Oriane Marmontel; Charlotte Decourt; Amandine Rubio; Séverine Nony; Sabrina Dumont; Charlotte Cuerq; Sybil Charrière; Philippe Moulin; Alain Lachaux; M Mahmood Hussain; Dominique Bozon; Noël Peretti
Journal:  Atherosclerosis       Date:  2019-03-03       Impact factor: 5.162

7.  A severe form of abetalipoproteinemia caused by new splicing mutations of microsomal triglyceride transfer protein (MTTP).

Authors:  Véronique Pons; Corinne Rolland; Michel Nauze; Marie Danjoux; Gérald Gaibelet; Anne Durandy; Agnès Sassolas; Emile Lévy; François Tercé; Xavier Collet; Emmanuel Mas
Journal:  Hum Mutat       Date:  2011-06-14       Impact factor: 4.878

8.  Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia.

Authors:  Lucia Magnolo; Mohamed Najah; Tatiana Fancello; Enza Di Leo; Elisa Pinotti; Ines Brini; Neji M Gueddiche; Sebastiano Calandra; Naceur M Slimene; Patrizia Tarugi
Journal:  Gene       Date:  2012-10-06       Impact factor: 3.688

9.  Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function.

Authors:  Meghan T Walsh; Jahangir Iqbal; Joby Josekutty; James Soh; Enza Di Leo; Eda Özaydin; Mehmet Gündüz; Patrizia Tarugi; M Mahmood Hussain
Journal:  Circ Cardiovasc Genet       Date:  2015-07-29

Review 10.  Microsomal triglyceride transfer protein and its role in apoB-lipoprotein assembly.

Authors:  M Mahmood Hussain; Jason Shi; Paul Dreizen
Journal:  J Lipid Res       Date:  2003-01       Impact factor: 5.922

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Authors:  Lauren S Talman; Ronald F Pfeiffer
Journal:  Mov Disord Clin Pract       Date:  2022-02-05

2.  Prospective Registry Study of Primary Dyslipidemia (PROLIPID): Rationale and Study Design.

Authors:  Hayato Tada; Tomoyuki Kurashina; Masatsune Ogura; Misa Takegami; Yoshihiro Miyamoto; Hidenori Arai; Mariko Harada-Shiba; Shun Ishibashi
Journal:  J Atheroscler Thromb       Date:  2021-10-22       Impact factor: 4.394

3.  Effects of the administration of Elovl5-dependent fatty acids on a spino-cerebellar ataxia 38 mouse model.

Authors:  Ilaria Balbo; Francesca Montarolo; Federica Genovese; Filippo Tempia; Eriola Hoxha
Journal:  Behav Brain Funct       Date:  2022-08-06       Impact factor: 3.950

  3 in total

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