Thursday, April 4, 2019
Physical Impacts of Alcohol Abuse
Physical Impacts of Alcohol AbuseAlcohol use and pervert can travel the coloured-colored, central nervous system and the kidneys. The conduct of the constant use of intoxicant can be renowned and examined in patients using numerous methods. These methods utilize the bodys reaction towards alcoholic drinkic beverage using biochemical markers like -glutamyl tranferase (GGT), high density lipoprotein cholesterol (HDL-C) and aspartate ami nonransferase (AST). Although biochemical markers can easily tell the clinician nigh the use and abuse of alcohol, genetic markers may also contri merelye to the dependence of alcohol.Alcohol use and abuse is associated with denary illnesses much(prenominal)(prenominal) as cirrhosis and alcoholic hepatitis. Alcohol outgo has many negative make that increase with age, ranging from short term reactions like dehydration and ethanol poisoning to chronic reactions like liver failure and alcoholic fatty liver disease. The result of alcohol consum ption is reactive changes in the body such as an increase of enzymatic activity and concentration as well as the step-down of enzymatic activity and concentration due to tissue destruction.The enzyme -glutamyl tranferase (GGT) activity is one of the most sensitive tests for alcohol use. The enzymes activity rises when there is acute hepatocellular damage act commonly is patients with alcoholic liver disease (G. Bbosa, D. Kyegombe, W. Anokbonggo, A. Lubega, A. Mugisha and J. Ogwal-Okeng, 2014). GGT is such a sensitive marker that the levels will also be increased even if no liverwort or biliary damage is present in the patient suffering from alcoholism. GGT levels increase drastically in the serum of patients abusing alcohol chronically, an increase of 2-3 times the normal value is most commonly present (S. Kavitha, V. Venkatraman and K. Jeyaprakash, 2013). GGT serum levels can also be raised in patients with digestive disorders and mostly only foretells alcoholism in patients wh o abuse the substance excessively.High density lipoprotein cholesterol (HDL-C) levels are more commonly decreased in older patients suffering from alcoholism than in younger patients and are employ rather as a confirmation marker than an initial indicator. The HDL-C levels in the serum will be decreased in the patients presenting with alcohol abuse (S. Kavitha, V. Venkatraman and K. Jeyaprakash, 2013).The enzyme aspartate aminotransferase (AST) can be used to indicate alcoholic liver disease and cirrhosis, barely proves difficult to provide accurate results in the absence of liver damage. The enzyme is also found in multiple other organs like the brain and the kidneys and is more likely to be used as a confirmation of liver disease than a definitive diagnosis (D. Adler, 2013). The levels of AST in the patients serum will be increased up to 4 times the normal ranges in cases of liver damage. The increased AST levels, when indicating alcoholic liver disease, is most likely due to ce llular necrosis due to excessive alcohol consumption.Alanine aminotransferase (ALT) is excessively produced in patients with hepatic injury and in alcoholic patients (M. Hyder, M. Hasan and A. Mohieldein, 2013). The disadvantage of this test in that the levels only significantly increases if severe hepatic damage is already present, but the major advantage is that ALT is only present in the liver (R. Van Dyke, 2012). ALT will be increased 4-6X in cases of alcoholic cirrhosis and 7-10X in cases of alcoholism with alcoholic liver disease.The ratio of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) can also indicate alcoholic liver disease with a ratio greater than 21 with respect to ASTALT. This result is mostly due to low ALT levels in the serum because of hepatic necrosis, pyridoxal-5-phosphate deficiency or mitochondrial AST flight (M. Adak, A. Thakur and K. Adhikari, 2012). The ratio is mostly used as an affirmative test as the ratio only rises preceding(pr enominal) 2 in severe cases of alcoholic liver disease.Sialic acidGenetic predispositions to alcoholism mystify not been completely identified, but studies have indicated genes that may be responsible. These genes are known as the Mpdz, the Kcnj9 and the GABRA2 genes. Although these genes are used theoretical markers rather than actual indicator to alcohol dependence there is a correlation amidst the severity of the withdrawal symptoms and the risk of alcohol dependence (K. Buck, L. Milner, D. Denmark, S. Grant and L. Kozell, 2012).The GABRA2 gene is located on chromosome 4p12 and regulates the yield of gamma-amino butyric acid (GABA) which acts as an inhibitory neurotransmitter (U.S. National Library of Medicine, 2014). Alcohol can affect the signalling road of the GABA system if a variation is present in the GABRA2 gene increasing the pleasure derived from the consumption of alcohol above normal levels which can greatly increase the risk of alcoholism in the persons who have th is variation (D. Dick and A. Agrawal, 2008).Alcoholism poses a serious health threat to the medical community do many serious complications in a healthy lifestyle. Testing for GGT is seen as the most sensitive test, but has the one drawback of having quite a bit of interferences, which can be cancelled out if brought into the equation. ALT and AST tests the livers oecumenical homeostasis and should rather be handled as a complimentary test along with a test such as GGT in order to confirm a diagnosis. Genetic markers for alcohol abuse have not been fully discovered as of yet, although a variation in GABRA2 is known to increase the risk of alcohol dependence due to its effects on the GABA pathway when alcohol is consumed.ReferencesG. Bbosa, D. Kyegombe, W. Anokbonggo, A. Lubega, A. Mugisha and J. Ogwal-Okeng. (2014). Chronic Alcohol outlay Affects Serum Enzymes Levels in the HIV-Infected Patients on Stavudine (d4T)/Lamivudine (3TC)/Nevirapine (NVP) Treatment Regimen. Pharmacology Pharmacy. 1 (5), 181-194.M. Adak, A. Thakur and K. Adhikari. (2012). Study of biochemical Markers in Alcoholic Liver Disease Hospital-Based Case Control Study. explore Journal of Pharmaceutical, Biological and chemical Sciences. 3 (3), 987-995.S. Kavitha, V. Venkatraman and K. Jeyaprakash. (2013). biochemical Markers and Age Onset Involved In Heavy Alcoholism.Asian Journal of Biochemical and Pharmaceutical Research. 4 (1), 80-87.D. Adler. (2013). The Difficulty of using a Biological Marker for Alcohol Use A Recent Historical Overview.Sound Neuroscience An Undergraduate Neuroscience Journal. 1 (1), 1-8.K. Buck, L. Milner, D. Denmark, S. Grant and L. Kozell. (2012). Discovering genes Involved in Alcohol dependency and other Alcohol responses Role of Animal Models.Alcohol Research Current Reviews. 367-374.U.S. National Library of Medicine. (2014).GABRA2. easy http//ghr.nlm.nih.gov/gene/GABRA2. Last accessed 02 September 2014.D. Dick and A. Agrawal. (2008). The Genetics of Alcohol a nd Other Drug Dependence.Alcohol Research Health. 31 (2), 111-118.R. Van Dyke. (2012). Liver Tests Use and Interpretation.Open Michigan. 1 (1), 1-60.M. Hyder, M. Hasan and A. Mohieldein. (2013). Comparative Levels of ALT, AST, ALP and GGT in Liver associated Diseases.European Journal of Experimental Biology. 3 (2), 280-284.
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment