Background: The aim of this study was to analyze the corrected QT interval (QTc), its dispersion (QTcd), and the QT interval index (QTcI) and to compare it with the corrected JT interval (JTc), its dispersion (JTcd), and the JT interval index (JTcI) in long-term alcoholic users, by investigating the ventricular activation until the completion of repolarization.
Methods: The study of ECGs was performed on a selected group of 49 male white alcoholic patients, mean age 53.51+/-4.78 years. The control group was pair-matched. The analysis of ECGs was performed according to the Minnesota Code, and Bazett's formula gave the values of the corrected QT interval and JT interval.
Results: The results of the descriptive statistics in the group of alcoholics showed a range of the QTcd of 12.0 to 103.0 milliseconds, mean 44.2+/-18.6 milliseconds, compared with 5.0 to 68.0 milliseconds, mean 23.8+/-11.1 milliseconds, in the control group (p < 0.0001). The range of JTcd in the alcoholic patients was 11.0 to 88.0 milliseconds, mean 43.0+/-18.3 milliseconds, compared with 5.0 to 66.0 milliseconds, mean 22.8+/-12.1 milliseconds, in the control group (p < 0.0001). The QTc from 422.0 to 480.0 milliseconds was obtained in 69.4% of the alcoholic patients and 32.6% of the controls. The QTc over 480.0 milliseconds was found in 24.5% of the alcoholic patients, but was not recorded among the controls at all (p < 0.0001). The QTcd over 50.0 milliseconds was registered in 34.7% of the alcoholic patients, while in the controls a QTcd above 50 milliseconds was found in 2.0% (p < 0.0001). The mean values of QT were markedly higher in the alcoholic patients (p < 0.01) than in the controls. The same was the case with the values of QTd, QT(I), QTcd, and QTcI (p < 0.0001). Also, the mean values of JTd, JT(I), JTc, JTcd, and JTcI were significantly higher in the alcoholic patients than in the controls (p < 0.0001). The mean value of JT, although higher in the alcoholic patients, did not significantly differ between the examined groups (p=0.1002). The odds ratio estimated for prolonged QTc and for enlarged QTcd in the alcoholics versus the controls was 31.625 and 25.500 (p < 0.0001), respectively.
Conclusions: Persons who consume various alcoholic beverages excessively and for a long time have significantly higher dispersions of the QTc and JTc, intervals and they have a significantly higher estimation of relative risk for the prolonged QTc interval and higher QTc dispersion than the control group, i.e., higher risk of arrhythmias.
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http://dx.doi.org/10.1111/j.1530-0277.2006.00018.x | DOI Listing |
Metab Brain Dis
January 2025
Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus N, Denmark.
Background & Aims: Hepatic encephalopathy (HE), one of the most serious prognostic factors for mortality in alcohol-related cirrhosis (ALD cirrhosis), is not recorded in Danish healthcare registries. However, treatment of HE with lactulose, the universal first-line treatment, can be identified through data on filled prescriptions. This study aimed to investigate if lactulose can be used as a surrogate marker of HE.
View Article and Find Full Text PDFBiochem Genet
January 2025
Department of Gynecology, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
This study aimed to identify shared gene expression related to circadian rhythm disruption in polycystic ovary syndrome (PCOS) and non-alcoholic fatty liver disease (NAFLD) to discover common diagnostic biomarkers. Visceral fat RNA samples were collected from 12 PCOS and 14 non-PCOS patients, a sample size representing the clinical situation and sufficient to capture PCOS gene expression profiles. Along with liver transcriptome profiles from NAFLD patients, these data were analyzed to identify crosstalk circadian rhythm-related genes (CRRGs) between the diseases.
View Article and Find Full Text PDFCurr Cardiol Rep
January 2025
Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Purpose Of Review: Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common chronic liver disease, characterized by hepatic steatosis with at least one cardiometabolic risk factor. Patients with MASLD are at increased risk for the occurrence of cardiovascular events. Within this review article, we aimed to provide an update on the pathophysiology of MASLD, its interplay with cardiovascular disease, and current treatment strategies.
View Article and Find Full Text PDFJ Clin Pathol
January 2025
Institute of Liver Studies, King's College Hospital, London, UK
Aims: To reveal clinicopathological characteristics of alcoholic foamy degeneration (AFD)-an uncommon form of alcoholic liver injury.
Methods: Clinicopathological features of AFD (n=9) were examined in comparison to those of severe alcoholic hepatitis (SAH; n=12).
Results: Patients with AFD presented with either biochemical liver dysfunction (n=1) or clinical jaundice (n=8).
Neuroscience
January 2025
Department of Radiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210008 China; Medical Imaging Center, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210008 China; Institute of Medical Imaging and Artificial Intelligence, Nanjing University, Nanjing 210008 China; Institute of Brain Science, Nanjing University, Nanjing, China. Electronic address:
Type 2 diabetes (T2D) is often accompanied by non-alcoholic fatty liver disease (NAFLD), both of which are related to brain damage and cognitive impairment. However, cortical structural alteration and its relationship with metabolism and cognition in T2D with NAFLD (T2NAFLD) and without NAFLD (T2noNAFLD) remain unclear. The brain MRI scans, clinical measures and neuropsychological test were evaluated in 50 normal controls (NC), 73 T2noNAFLD, and 58 T2NAFLD.
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