Harleen Sood, Rupinderjeet Kaur, R. Garg, K. Shourya
{"title":"RELATION OF SERUM TOTAL TESTOSTERONE WITH SYMPTOMATOLOGY, COMPLICATIONS AND SEVERITY OF CHRONIC LIVER DISEASE IN MALE CIRRHOTICS","authors":"Harleen Sood, Rupinderjeet Kaur, R. Garg, K. Shourya","doi":"10.36106/ijar/9300403","DOIUrl":null,"url":null,"abstract":"Background: It has been seen that Testosterone (T) levels are generally low in men with advanced liver disease and\nprogressively fall with increasing severity of liver disease. This may lead to the development of various clinical sequelae\nof advanced liver disease and adverse outcomes. Objectives: The study was done with an objective to assess serum testosterone in liver cirrhosis\nand to determine the relation of serum testosterone with symptomatology, complications and severity of liver cirrhosis in male patients.\nMethods: The observational study was carried out in G.G.S. Medical College and Hospital, Faridkot (Punjab, India). One hundred males of age\n20-70 years with ultrasonographically proven cirrhosis of liver were included in the study. Demographic and clinical details of the patients were\nnoted in the pre-designed proforma. Levels of serum total testosterone were measured in every patient. Laboratory investigations and Ultrasound\nof abdomen (with liver elastography) for cirrhosis liver was done. The severity of the disease was assessed by CTP and MELD score. Results:\nSignicant negative correlation of serum total testosterone was seen with MELD score, total bilirubin, ALP. Non signicant mild positive\ncorrelation was seen between serum total testosterone with serum albumin levels, blood platelet count, serum sodium levels and AFP. We found\nsignicant association of low Testosterone levels with high CTP (p=0.007) and high MELD scores (p=0.042). No signicant association of\ncomplications was found with low testosterone. No association was seen with age, etiological factors or symptomatology except presence of\njaundice. Conclusion: We identify low testosterone as a novel biomarker that is associated with increased severity of cirrhosis liver in men. This\nstudy provides a strong rationale to conduct adequately powered interventional trials to determine whether testosterone therapy can improve\nsurvival and other outcomes in this population.","PeriodicalId":13502,"journal":{"name":"Indian journal of applied research","volume":"93 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian journal of applied research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36106/ijar/9300403","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: It has been seen that Testosterone (T) levels are generally low in men with advanced liver disease and
progressively fall with increasing severity of liver disease. This may lead to the development of various clinical sequelae
of advanced liver disease and adverse outcomes. Objectives: The study was done with an objective to assess serum testosterone in liver cirrhosis
and to determine the relation of serum testosterone with symptomatology, complications and severity of liver cirrhosis in male patients.
Methods: The observational study was carried out in G.G.S. Medical College and Hospital, Faridkot (Punjab, India). One hundred males of age
20-70 years with ultrasonographically proven cirrhosis of liver were included in the study. Demographic and clinical details of the patients were
noted in the pre-designed proforma. Levels of serum total testosterone were measured in every patient. Laboratory investigations and Ultrasound
of abdomen (with liver elastography) for cirrhosis liver was done. The severity of the disease was assessed by CTP and MELD score. Results:
Signicant negative correlation of serum total testosterone was seen with MELD score, total bilirubin, ALP. Non signicant mild positive
correlation was seen between serum total testosterone with serum albumin levels, blood platelet count, serum sodium levels and AFP. We found
signicant association of low Testosterone levels with high CTP (p=0.007) and high MELD scores (p=0.042). No signicant association of
complications was found with low testosterone. No association was seen with age, etiological factors or symptomatology except presence of
jaundice. Conclusion: We identify low testosterone as a novel biomarker that is associated with increased severity of cirrhosis liver in men. This
study provides a strong rationale to conduct adequately powered interventional trials to determine whether testosterone therapy can improve
survival and other outcomes in this population.