The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease
- PMID: 15355491
- DOI: 10.1111/j.1600-0404.2004.00315.x
The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease
Abstract
Objectives: The etiology of sporadic idiopathic Parkinson's disease (PD) is considered multifactorial with both genetic and environmental factors modifying the disease expression. Recent studies suggest that polymorphism in monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) might influence the risk and treatment of PD. The aim of the study was to evaluate the effect of MAOB and COMT genetic polymorphism on effective daily dose of levodopa applied during the first 5 years of treatment, and to find out if a relationship exists between MAOB and COMT haplotypes and motor disturbances onset in PD patients treated with levodopa preparations.
Materials and methods: A total of 95 patients (40 females and 55 males) of Polish origin diagnosed with sporadic PD were enrolled into the study, and were divided into two groups. Group 1 - patients treated with doses of levodopa below 500 mg/day during the first 5 years of treatment. Group 2 - patients requiring levodopa doses exceeding 500 mg/24 h during the first 5 years of treatment. Low activity alleles of MAOB and COMT, i.e. MAOB allele A and COMT(L) as well as high activity ones, i.e. MAOB allele G and COMT(H), were determined using PCR-RFLP method.
Results: No statistically significant differences were found in MAOB and COMT allele distribution in the two groups. However, the frequency of COMT(L/L) homozygotes was higher in the group treated with low doses of levodopa when compared with the second group. MAOB and COMT AG-HH haplotype predominated in the group of females treated with high daily doses of levodopa when compared with AG-LL haplotype in the group of females treated with low daily doses of levodopa (<500 mg/24 h).
Conclusion: The results of the study suggest that patients with COMT(L/L) genotype and possibly MAOB genotype A may benefit from more efficient and safer levodopa therapy.
Similar articles
-
The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications.Pharmacogenet Genomics. 2008 Sep;18(9):815-21. doi: 10.1097/FPC.0b013e328306c2f2. Pharmacogenet Genomics. 2008. PMID: 18698234 Clinical Trial.
-
The catechol-O-methyltransferase and monoamine oxidase B polymorphisms and levodopa therapy in the Iranian patients with sporadic Parkinson's disease.Acta Neurobiol Exp (Wars). 2012;72(3):272-82. doi: 10.55782/ane-2012-1900. Acta Neurobiol Exp (Wars). 2012. PMID: 23093014
-
Catechol-O-methyltransferase and monoamine oxidase B genes and susceptibility to sporadic Parkinson's disease in a Polish population.Eur Neurol. 2005;53(2):68-73. doi: 10.1159/000084302. Epub 2005 Mar 7. Eur Neurol. 2005. PMID: 15753616
-
Catechol-O-methyltransferase and Parkinson's disease.Acta Med Okayama. 2002 Feb;56(1):1-6. doi: 10.18926/AMO/31725. Acta Med Okayama. 2002. PMID: 11873938 Review.
-
Catechol-O-methyl transferase (COMT) inhibitors in patients with Parkinson's disease: is COMT genotype a useful indicator of clinical efficacy?Am J Pharmacogenomics. 2003;3(1):11-5. Am J Pharmacogenomics. 2003. PMID: 12562212 Review.
Cited by
-
Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic women.Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):793-8. doi: 10.1002/ajmg.b.30716. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18270997 Free PMC article.
-
A systematic review and integrative approach to decode the common molecular link between levodopa response and Parkinson's disease.BMC Med Genomics. 2017 Sep 19;10(1):56. doi: 10.1186/s12920-017-0291-0. BMC Med Genomics. 2017. PMID: 28927418 Free PMC article.
-
A Systematic Review of Parkinson's Disease Pharmacogenomics: Is There Time for Translation into the Clinics?Int J Mol Sci. 2021 Jul 5;22(13):7213. doi: 10.3390/ijms22137213. Int J Mol Sci. 2021. PMID: 34281267 Free PMC article.
-
Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson's disease.Brain. 2015 May;138(Pt 5):1271-83. doi: 10.1093/brain/awv063. Epub 2015 Mar 23. Brain. 2015. PMID: 25805645 Free PMC article. Clinical Trial.
-
Association of COMT rs4680 and MAO-B rs1799836 polymorphisms with levodopa-induced dyskinesia in Parkinson's disease-a meta-analysis.Neurol Sci. 2021 Oct;42(10):4085-4094. doi: 10.1007/s10072-021-05509-3. Epub 2021 Aug 4. Neurol Sci. 2021. PMID: 34346015 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous