Aminoacidopathies: Prevalence, Etiology, Screening, and Treatment Options.
Abstract |
Inborn errors of metabolism (IEMs) are a group of inherited metabolic disorders which are caused by mutations in the specific genes that lead to impaired proteins or enzymes production. Different metabolic pathways are perturbed due to the deficiency or lack of enzymes. To date, more than 500 IEMs have been reported with most of them being untreatable. However, fortunately 91 such disorders are potentially treatable, if diagnosed at an earlier stage of life. IEMs have been classified into different categories and one class of IEMs, characterized by the physiological disturbances of amino acids is called as aminoacidopathies. Out of 91 treatable IEM, thirteen disorders are amino acid related. Aminoacidopathies can be detected by chromatography and mass spectrometry based analytical techniques (e.g., HPLC, GC-MS, LC-MS/MS) for amino acid level changes, and through genetic assays (e.g., PCR, TaqMan Genotyping, DNA sequencing) at the mutation level in the corresponding genes. Hence, this review is focused to describe thirteen common aminoacidopathies namely: Phenylketonuria (PKU), Maple Syrup Urine Disease (MSUD), Homocystinuria/ Methylene Tetrahydrofolate Reductase ( MTHFR) deficiency, Tyrosinemia type II, Citrullinemia type I and type II, Argininosuccinic aciduria, Carbamoyl Phosphate Synthetase I (CPS) deficiency, Argininemia ( arginase deficiency), Hyperornithinemia-Hyperammonemia-Homocitrullinuria ( HHH) syndrome, N-Acetylglutamate Synthase ( NAGS) deficiency, Ornithine Transcarbamylase ( OTC) deficiency, and Pyruvate Dehydrogenase (PDH) complex deficiency. Furthermore, the etiology, prevalence and commonly used analytical techniques for screening of aminoacidopathies are briefly described. This information would be helpful to researchers and clinicians especially from developing countries to initiate newborn screening programs for aminoacidopathies.
|
Authors | Muhammad Wasim, Fazli Rabbi Awan, Haq Nawaz Khan, Abdul Tawab, Mazhar Iqbal, Hina Ayesha |
Journal | Biochemical genetics
(Biochem Genet)
Vol. 56
Issue 1-2
Pg. 7-21
(Apr 2018)
ISSN: 1573-4927 [Electronic] United States |
PMID | 29094226
(Publication Type: Journal Article, Review)
|
Chemical References |
|
Topics |
- Amino Acid Metabolism, Inborn Errors
(diagnosis, epidemiology, etiology, therapy)
- Amino Acids
(blood, genetics)
- Genotyping Techniques
- Humans
- Mass Screening
- Mass Spectrometry
- Prevalence
|
|
Join CureHunter, for free Research Interface BASIC access!
Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease.
Find out why thousands of doctors, pharma researchers and patient activists
around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!
|