Influence of polymorphic N-acetyltransferases on non-malignant spontaneous disorders and on response to drugs

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This paper examines the influence of polymorphic N-acetyltransferases on spontaneous disorders and drug responses, concluding that NAT2 polymorphism is not related to endometriosis risk despite its potential role in other conditions.

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This review examines the role of polymorphic N-acetyltransferases (NAT1 and NAT2) in the detoxification of xenobiotics and their potential association with various non-malignant spontaneous disorders. The author notes that while a link between NAT2 polymorphism and conditions like systemic lupus erythematosus, inflammatory bowel disease, and endometriosis has been definitively discarded, evidence for other diseases such as rheumatoid arthritis remains inconclusive. The paper highlights that slow metabolizers are more susceptible to side effects from certain drugs, including hydralazine-induced SLE-like syndromes and sulphonamide rashes. Relevance to endometriosis: listed as one condition where a relation with NAT2 polymorphism has been definitely discarded, though the paper's main focus is drug metabolism and autoimmune or degenerative diseases.

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Abstract

Polymorphic N-acetyl transferases (NAT) 1 and 2 are involved in detoxification of xenobiotic arylamines and hydralazines. These common environmental chemicals may be related to the pathogenesis of many spontaneous disorders, mainly malignancies, but also disimmune or degenerative diseases, for which a polygenic predisposition has been suggested. Hence, polymorphic NAT genes (NAT2 has been the most studied one) may be low-penetrance risk genes for some of these disorders. Although a relation of risk may be definitely discarded for systemic lupus erythematosus (SLE), inflammatory bowel disease and endometriosis, more research is needed for rheumatoid arthritis, Parkinson's, Alzheimer's, Behçet's and periodontal diseases , as current results are inconclusive but suggest a possible relation with NAT2 polymorphism. In diabetes mellitus the possible relation with the rapid phenotype may be due to acquired metabolic changes and more genotyping studies are needed. NAT2 slow metabolizers are more prone to the side effects of polymorphically acetylated drugs, as is the SLE-like syndrome induced by hydralazine and procainamide, the side effects due to sulphasalazine and the skin rash secondary to many sulphonamides. Future research should be based on well-designed studies, with adequate sample sizes and homogeneous recruitment criteria, to obviate the proliferation of small studies that are time- and resource-consuming without offering definite answers.
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Abstract

Keywords: N-acetyl transferases, acetylator polymorphism, Alzheimer's disease, Parkinson's disease, diabetes mellitus, rheumatoid arthritis, autoimmune diseases, drug response, side effects Current Drug Metabolism Title: Influence of Polymorphic N-Acetyltransferases on Non-Malignant Spontaneous Disorders and on Response to Drugs Volume: 9 Issue: 6 Author(s): J. M. Ladero Affiliation:

Keywords

N-acetyl transferases, acetylator polymorphism, Alzheimer's disease, Parkinson's disease, diabetes mellitus, rheumatoid arthritis, autoimmune diseases, drug response, side effects

Abstract

Polymorphic N-acetyl transferases (NAT) 1 and 2 are involved in detoxification of xenobiotic arylamines and hydralazines. These common environmental chemicals may be related to the pathogenesis of many spontaneous disorders, mainly malignancies, but also disimmune or degenerative diseases, for which a polygenic predisposition has been suggested. Hence, polymorphic NAT genes (NAT2 has been the most studied one) may be low-penetrance risk genes for some of these disorders. Although a relation of risk may be definitely discarded for systemic lupus erythematosus (SLE), inflammatory bowel disease and endometriosis, more research is needed for rheumatoid arthritis, Parkinsons, Alzheimers, Behcets and periodontal diseases , as current results are inconclusive but suggest a possible relation with NAT2 polymorphism. In diabetes mellitus the possible relation with the rapid phenotype may be due to acquired metabolic changes and more genotyping studies are needed. NAT2 slow metabolizers are more prone to the side effects of polymorphically acetylated drugs, as is the SLE-like syndrome induced by hydralazine and procainamide, the side effects due to sulphasalazine and the skin rash secondary to many sulphonamides. Future research should be based on well-designed studies, with adequate sample sizes and homogeneous recruitment criteria, to obviate the proliferation of small studies that are time- and resource-consuming without offering definite answers. Export Options About this article Cite this article as: Ladero M. J., Influence of Polymorphic N-Acetyltransferases on Non-Malignant Spontaneous Disorders and on Response to Drugs, Current Drug Metabolism 2008; 9 (6) . https://dx.doi.org/10.2174/138920008784892038 | DOI https://dx.doi.org/10.2174/138920008784892038 | Print ISSN 1389-2002 | | Publisher Name Bentham Science Publishers | Online ISSN 1875-5453 | Call for Papers in Thematic Issues Drug Metabolism in Cancer Immunotherapy and Next-Gen Therapeutics: Mechanistic Insights and the Impact of Co-administered Drugs Drug Metabolism in Cancer Immunotherapy and Next-Gen Therapeutics: Mechanistic Insights and the Impact of Co-administered Drugs" aims to highlight the emerging insights into how metabolic processes affect the safety, efficacy, and ADMET (Absorption, Distribution, Metabolism, Excretion, and Toxicity) profiles and Pharmacodynamics of emerging anticancer therapies when used alone or in ...read more Innovative Therapeutic Approaches in Infectious Diseases Infectious diseases continue to challenge global health systems due to rising antimicrobial resistance, emerging pathogens, and increasing drug tolerance. 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endometriosis

MeSH descriptors

Acetyltransferases Acetyltransferases Autoimmune Diseases Neurodegenerative Diseases Pharmaceutical Preparations Acetylation Acetylation Acetyltransferases Acetyltransferases Animals Animals Autoimmune Diseases Autoimmune Diseases Autoimmune Diseases Humans Humans Neurodegenerative Diseases Neurodegenerative Diseases Neurodegenerative Diseases Pharmaceutical Preparations

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