25 results on '"Samuel S Lee"'
Search Results
2. The liver–heart relationship: a history
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Hongqun Liu and Samuel S. Lee
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- 2023
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3. List of contributors
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Juan Gonzalez Abraldes, Mario Altieri, Vicente Arroyo, Dina Attia, Anna Baiges, Soon Koo Baik, Fabian Betancourt, Ryan Chadha, Daljeet Chahal, Po-Hung Chen, Moreshwar S. Desai, Iliana Doycheva, Javier Fernandez, Yasser Fouad, Juan Carlos García-Pagán, Noelle Gorgis, Harini Gurram, Virginia Hernández-Gea, Shaz Iqbal, Manhal Izzy, Jennifer Jo, Seong Hee Kang, Rofida Khalifa, Masahiro Koseki, Masanari Kuwabara, Samuel S. Lee, Ton Lisman, Hongqun Liu, Xuefeng Luo, Marta Magaz, Vladimir Marquez, Richard Moreau, Oana Nicoar-Farcu, Koichiro Niwa, Atsushi Okada, P. Timothy Pollak, Yuki Saito, Bonifasius S. Singu, Guillem Soy, Tatsunori Taniguchi, Fanny Turon, Paradis Valérie, Lisa B. VanWagner, Roger K. Verbeeck, Kymberly D. Watt, Florence Wong, and Christopher L. Wray
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- 2023
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4. Cirrhotic cardiomyopathy
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Hongqun Liu, Daljeet Chahal, Vladimir Marquez, and Samuel S. Lee
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- 2023
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5. Novel variant in glycophorin c gene protects against ribavirin-induced anemia during chronic hepatitis C treatment
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Eric M. Yoshida, Britt I. Drögemöller, Jessica N. Trueman, Samuel S. Lee, Catrina M Loucks, Jennifer J. Lin, Bandar Al-Judaibi, Colin J. D. Ross, Alnoor Ramji, Jo-Ann Ford, Bruce Carleton, Ute I. Schwarz, Richard B. Kim, Galen E B Wright, and Edward Tam
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Hemolytic anemia ,Male ,Anemia, Hemolytic ,Canada ,Pharmacogenomic Variants ,Anemia ,RM1-950 ,Calcitriol receptor ,Antiviral Agents ,Risk Assessment ,chemistry.chemical_compound ,Risk Factors ,Ribavirin ,Medicine ,Humans ,Glycophorins ,Prospective Studies ,Pyrophosphatases ,Adverse effect ,Aged ,Pharmacology ,business.industry ,General Medicine ,Glycophorin C ,Hepatitis C, Chronic ,Middle Aged ,medicine.disease ,Pharmacogenomic Testing ,chemistry ,Pharmacogenetics ,Case-Control Studies ,Immunology ,HCV ,Receptors, Calcitriol ,Female ,ITPA ,Hemoglobin ,Therapeutics. Pharmacology ,business ,Pharmacogenomics ,Adverse reactions ,Genome-Wide Association Study - Abstract
Background The current use of ribavirin in difficult-to-cure chronic hepatitis C patients (HCV) and patients with severe respiratory infections is constrained by the issue of ribavirin-induced hemolytic anemia that affects 30% of treated patients, requiring dosage modification or discontinuation. Though some genetic variants have been identified predicting this adverse effect, known clinical and genetic factors do not entirely explain the risk of ribavirin-induced anemia. Methods We assessed the associations of previously identified variants in inosine triphosphatase (ITPA), solute carrier 28A2 (SLC28A2) and vitamin D receptor (VDR) genes with ribavirin-induced anemia defined as hemoglobin decline of ≥30 g/L on treatment, followed by a staged discovery (n = 114), replication (n = 74), and combined (n = 188) genome-wide association study to uncover potential new predictive variants. Results We identified a novel association in the gene coding glycophorin C (rs6741425; OR:0.12, 95%CI:0.04–0.34, P = 2.94 × 10-6) that predicts protection against ribavirin-induced anemia. We also replicated the associations of ITPA and VDR genetic variants with the development of ribavirin-induced anemia (rs1127354; OR:0.13, 95%CI:0.04–0.41, P = 8.66 ×10-5; and rs1544410; OR:1.65, 95%CI:1.01–2.70, P = 0.0437). Conclusions GYPC variation affecting erythrocyte membrane strength is important in predicting risk for developing ribavirin-induced anemia. ITPA and VDR genetic variants are also important predictors of this adverse reaction.
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- 2021
6. Long-Term Follow-up and Quantitative Hepatitis B Surface Antigen Monitoring in North American Chronic HBV Carriers
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Mark G. Swain, Carla S. Coffin, Kelly W. Burak, Conar R. O’Neil, Samuel S. Lee, Meredith A. Borman, Carmen L. Charlton, Stephen E. Congly, Carla Osiowy, and M. Sarah Rose
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Adult ,Male ,0301 basic medicine ,Hepatitis B virus ,HBsAg ,medicine.medical_specialty ,Canada ,Time Factors ,Specialties of internal medicine ,Antiviral Agents ,Gastroenterology ,03 medical and health sciences ,Hepatitis B, Chronic ,0302 clinical medicine ,Disease Phase ,Predictive Value of Tests ,Internal medicine ,medicine ,Humans ,Retrospective Studies ,Hepatitis B Surface Antigens ,Hepatology ,Nucleoside analogue ,business.industry ,Reproducibility of Results ,Lamivudine ,Retrospective cohort study ,General Medicine ,Entecavir ,Middle Aged ,Viral Load ,Discontinuation ,Treatment Outcome ,030104 developmental biology ,HBeAg ,RC581-951 ,DNA, Viral ,Cohort ,Diagnostic Test ,Female ,030211 gastroenterology & hepatology ,Drug Monitoring ,Chronic Hepatitis B ,business ,Nucleoside Analogues ,Biomarkers ,Follow-Up Studies ,medicine.drug ,Natural History - Abstract
Introduction. Quantitative hepatitis B surface antigen (qHBsAg) combined with HBV DNA may be useful for predicting chronic hepatitis B (CHB) activity and nucleoside analogue (NA) response.Material and methods. In this retrospective cohort study we evaluated qHBsAg levels according to CHB disease phase and among patients on treatment. Random effect logistic regression analysis was used to analyze qHBsAg change with time in the NA-treated cohort.Results. 545 CHB carriers [56% M, median age 48 y (IQR 38-59), 73% Asian] had qHBsAg testing. In the untreated group (44%), 8% were classified as immune tolerant, 10% immune clearance, 40% inactive, and 43% had HBeAg- CHB and the median HBsAg levels were 4.6 (IQR 3.4-4.9), 4.0 (IQR 3.4-4.5), 2.9 (IQR 1.4-3.8), and 3.2 log IU/mL (IQR 2.6-4.0), respectively; p < 0.001. In the NA-treated group (28% entecavir, 68% tenofovir, 4% lamivudine), no significant change in qHBsAg levels occured with time. However, 19% of patients on long-term NA had sustained qHBsAg < 2 log10 IU/mL.Conclusion. qHBsAg titers were associated with CHB phase and remained stable in those on long-term NA. A significant number of treated patients had low-level qHBsAg, of which some may be eligible for treatment discontinuation without risk of flare.
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- 2018
7. Cirrhotic Cardiomyopathy
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Waleed Al Hamoudi and Samuel S. Lee
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QT interval ,medicine.medical_specialty ,Cardiac output ,Cirrhosis ,systolic function ,medicine.medical_treatment ,heart failure ,Specialties of internal medicine ,Liver transplantation ,Hepatorenal syndrome ,Internal medicine ,medicine ,Hepatopulmonary syndrome ,Hepatology ,business.industry ,diastolic function ,General Medicine ,medicine.disease ,Cirrhotic cardiomyopathy ,RC581-951 ,Hyperdynamic circulation ,Cardiology ,cardiac complications ,business ,Transjugular intrahepatic portosystemic shunt - Abstract
Liver cirrhosis is associated with a wide range of cardiovascular abnormalities. These abnormalities include hyperdynamic circulation characterized by an increase in cardiac output and a decrease in peripheral vascular resistance. Despite the increased cardiac output, impaired ventricular contractility in response to both physiological and pharmacological stimuli has been described. Other cardiac abnormalities include structural changes including enlargement or hypertrophy of different cardiac chambers and electrophysiological changes such as QT prolongation. This constellation of cardiac abnormalities is termed cirrhotic cardiomyopathy. The pathogenic mechanisms of cirrhotic cardiomyopathy are multifactorial and include cardiomyocyte plasma membrane physico-chemical changes, attenuated stimulatory pathways, and enhanced activity of inhibitory systems. Accumulating evidence suggests that cirrhotic cardiomyopathy plays a major role in the pathogenesis of cardiac dysfunction following liver transplantation or transjugular intrahepatic portosystemic shunt placement. Recent research also strongly suggests that cirrhotic cardiomyopathy contributes to the pathogenesis of hepatorenal syndrome, especially following infections such as spontaneous bacterial peritonitis. Treatment of this syndrome remains largely empirical. Successful liver transplantation is thought to improve all the organ-related hemodynamic dysfunctions, including hepatopulmonary syndrome, cerebral hypoperfusion, hepatorenal syndrome, and cirrhotic cardiomyopathy. The prolonged QT interval normalizes following liver transplantation. Thus, liver transplantation appears to be the ultimate treatment for the cardiovascular complications of cirrhosis.
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- 2006
8. Cardiovascular Complications of Cirrhosis
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Soon Koo Baik and Samuel S. Lee
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medicine.medical_specialty ,Cirrhosis ,business.industry ,Internal medicine ,medicine ,medicine.disease ,business ,Gastroenterology - Published
- 2012
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9. Contributors
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Paul C. Adams, Helmut Albrecht, Jasmohan Bajaj, Soon Koo Baik, Ulrich Beuers, Scott W. Biggins, Henri Bismuth, Kirsten Muri Boberg, Herbert L. Bonkovsky, Jaime Bosch, Thomas D. Boyer, Elizabeth M. Brunt, Martin Caselitz, Wolfgang H. Caselmann, Matt Cave, Henry Lik-Yuen Chan, Kyong-Mi Chang, Alessia Ciancio, Massimo Colombo, Hari S. Conjeevaram, Diane W. Cox, Chris P. Day, R. Brian Doctor, Ronald P.J. Oude Elferink, Scott A. Elisofon, Hashem B. El-Serag, Gamal Esmat, Gregory T. Everson, Keith Cameron Falkner, Michael B. Fallon, Sandy Feng, Hans-Peter Fischer, Brett E. Fortune, Scott L. Friedman, J.C. García-Pagán, Guadalupe Garcia-Tsao, Fayez K. Ghishan, Gregory J. Gores, Rainer W. Gruessner, Sanjeev Gupta, Ghassan M. Hammoud, E.J. Heathcote, Steve M. Helmke, G.M. Hirschfield, Douglas Hunt, Massimo Iavarone, Jamal A. Ibdah, Françoise Imbert-Bismut, Peter L.M. Jansen, Benjamin F. Johnson, Maureen M. F. Jonas, Dean P. Jones, Patrick S. Kamath, Tom H. Karlsen, Deirdre Kelly, J. Kettelle, Khalid M. Khan, Percy Knolle, David J. Kramer, Manoj Kumar, Navaneeth C. Kumar, Jennifer C. Lai, Réal Lapointe, Konstantinos N. Lazaridis, André Lechel, Samuel S. Lee, Riccardo Lencioni, Cynthia Levy, Keith D. Lindor, Stephen Locarnini, Anna S.F. Lok, Harmeet Malhi, Michael P. Manns, Jorge A. Marrero, Craig McClain, Robert McCuskey, Barbara H. McGovern, John G. McHutchison, Darius Moradpour, Victor J. Navarro, James Neuberger, Moises I. Nevah R., Yulia A. Nevzorova, Heather M. Patton, François Penin, David Perlmutter, Aurélie Plessier, Thierry Poynard, Puneet Puri, Charles Rice, Mario Rizzetto, Eve A. Roberts, Don C. Rockey, Jayanta Roy-Chowdhury, Namita Roy-Chowdhury, K. Lenhard Rudolph, Mark W. Russo, Sammy Saab, Arun J. Sanyal, S.K. Sarin, Erik Schrumpf, Leonard B. Seeff, S. Seijo, Vijay H. Shah, Steven I. Shedlofsky, Daniel Shouval, Claude B. Sirlin, Maxwell L. Smith, Emmanuil Smorodinsky, Ulrich Spengler, Richard K. Sterling, Stephen F. Stewart, Doris B. Strader, Christian P. Strassburg, R. Todd Stravitz, Priti Sud, Mark S. Sulkowski, Jayant A. Talwalkar, Norah A. Terrault, Hans L. Tillmann, Christian Trautwein, Parsia A. Vagefi, Dominique Valla, Siegfried Wagner, Nadia Warner, Vincent Wai-Sun Wong, and Naglaa Zayed
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- 2012
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10. Three-year efficacy and safety of tenofovir disoproxil fumarate treatment for chronic hepatitis B
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Oya Ovunc Kurdas, Maria Buti, Iskren Kotzev, Elsa Mondou, Michael P. Manns, Andrea Snow–Lampart, Zahary Krastev, E. Jenny Heathcote, Selim Gürel, Edward Gane, J. Anderson, Samuel S. Lee, George Germanidis, Peter Buggisch, Huy N. Trinh, Konstantin Tchernev, Franck Rousseau, Jeff Sorbel, Patrick Marcellin, Mitchell L. Shiffman, Kelly Kaita, Robert A. de Man, Robert Flisiak, Frank Weilert, Katyna Borroto–Esoda, Uludağ Üniversitesi/Tıp Fakültesi/ İç Hastalıkları Anabilim Dalı., Gürel, Selim, and Gastroenterology & Hepatology
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Male ,Single drug dose ,HBsAg ,Hbeag-positive patients ,Rhinopharyngitis ,Gastroenterology ,Septic shock ,Adefovir ,Viral replication ,Emtricitabine ,Adefovir dipivoxil ,Drug safety ,virus diseases ,Double blind procedure ,Liver biopsy ,Serum hbsag ,Chronic hepatitis b ,Liver cell carcinoma ,Tenofovir disoproxil ,Randomized controlled trial ,Liver disease ,Human ,Diarrhea ,medicine.medical_specialty ,Organophosphonates ,Major clinical study ,Side effect ,DNA polymerase ,Antiviral Agents ,Article ,Hepatitis B, Chronic ,SDG 3 - Good Health and Well-being ,Humans ,Creatinine blood level ,Tenofovir ,Natural-history ,medicine.disease ,Monotherapy ,Virology ,digestive system diseases ,Influenza ,Drug resistance ,DNA, Viral ,Mutation ,Gastroenterology & hepatology ,Drug induced headache ,Amino acid substitution ,Biopsy ,medicine.disease_cause ,Virus Replication ,Hepatitis B E Antigen ,Entecavir ,Liver Cell Carcinoma ,Peginterferon alpha-2a ,Hepatitis B e Antigens ,Fatigue ,Randomized Controlled Trials as Topic ,Chronic hepatitis ,Priority journal ,Upper abdominal pain ,Attention disturbance ,medicine.diagnostic_test ,Alanine Transaminase ,Nausea ,Liposarcoma ,Hepatitis B ,Middle Aged ,Term-follow-up ,Add on therapy ,Treatment Outcome ,HBeAg ,Lamivudine ,Negative patients ,Alanine aminotransferase blood level ,Female ,Nucleotide ,medicine.drug ,Adult ,Hepatitis B virus ,Treatment withdrawal ,Adolescent ,Dizziness ,Young Adult ,Internal medicine ,Drug Resistance, Viral ,Virus DNA ,medicine ,Sustained response ,Hepatology ,business.industry ,Adenine ,Virus-infection ,Dna level ,Drug efficacy ,Alanine aminotransferase ,business ,Controlled study ,Follow-Up Studies - Abstract
BACKGROUND & AIMS: Tenofovir disoproxil fumarate (TDF), a nucleotide analogue and potent inhibitor of hepatitis B virus (HBV) polymerase, showed superior efficacy to adefovir dipivoxil in treatment of chronic hepatitis B through 48 weeks. We evaluated long-term efficacy and safety of TDF monotherapy in patients with chronic hepatitis B who were positive or negative for hepatitis B e antigen (HBeAg+ or HBeAg-). METHODS: After 48 weeks of double-blind comparison of TDF to adefovir dipivoxil, patients who underwent liver biopsy were eligible to continue the study on open-label TDF for 7 additional years; data presented were collected up to 3 years (week 144) from 85% of participants. Primary efficacy end points at week 144 included levels of HBV DNA and alanine aminotransferase, development of resistance mutations, and presence of HBeAg or hepatitis B surface antigen (HBsAg). RESULTS: At week 144, 87% of HBeAg- and 72% of HBeAg+ patients treated with TDF had levels of HBV DNA
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- 2011
11. Clinical Consequences of Liver Disease: Cardiovascular
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Soon Koo Baik and Samuel S. Lee
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Liver disease ,business.industry ,medicine ,Bioinformatics ,medicine.disease ,business - Published
- 2006
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12. Reply to: Correspondence on 'Cardiomyopathy in cirrhosis: From pathophysiology to clinical care'
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Hongqun Liu, Jwan A. Naser, Grace Lin, and Samuel S. Lee
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Diseases of the digestive system. Gastroenterology ,RC799-869 - Published
- 2024
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13. Clinical outcomes of esophageal squamous cell carcinoma in patients with cirrhosis
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Dae Gon Ryu, Mi Sook Yun, Hongqun Liu, Samuel S. Lee, and Sangjune Laurence Lee
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Esophageal cancer ,Squamous cell carcinoma ,Cirrhosis ,Medical physics. Medical radiology. Nuclear medicine ,R895-920 ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,RC254-282 - Abstract
Purpose: Alcohol consumption is a strong risk factor for both cirrhosis and esophageal squamous cell carcinoma (ESCC). Few studies have been conducted on the treatment of ESCC in patients with cirrhosis. This study aimed to analyze the clinical outcomes of ESCC in patients with cirrhosis. Materials and methods: Medical records of patients with esophageal cancer between January 2009 and December 2023 were retrospectively reviewed. A total of 479 patients with ESCC were included and divided into cirrhotic (n = 69) and non-cirrhotic (n = 410) groups. Clinical outcomes and survival according to treatment were compared between these groups. Results: The cirrhotic group was younger (median age 64 years vs. 69 years, p = 0.022) and had a higher proportion of male (97.1 % vs. 88.3 %, p = 0.042) than the non-cirrhotic group. Patients with cirrhosis were less likely to undergo surgery (31.9 % vs. 47.8 %, p = 0.015) and were more likely to receive no active cancer treatment (26.1 % vs. 13.7 %, p = 0.010). Overall survival was lower in the cirrhotic group (hazard ratio [HR], 1.41; 95 % confidence interval [CI], 1.01–1.99; p = 0.045), however, no difference was found between Child-Pugh class A patients and those in the non-cirrhotic group (HR, 1.04 [95 % CI, 0.69–1.56]; p = 0.864). Postoperative mortality was significantly higher in cirrhotic group (27.3 % vs. 8.7 %, p = 0.011). Upon performing concurrent chemoradiotherapy (CRT), the clinical complete response rate (84.2 % vs. 43.3 %, p = 0.004) was better in the cirrhotic group. CRT yielded better overall survival for patients with cancer in the resectable stages in the cirrhotic group compared to surgery (HR, 0.19 [95 % CI, 0.42–0.84]; p = 0.029]. Conclusions: In patient with ESCC and cirrhosis, chemoradiotherapy may be a better treatment option than surgery.
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- 2024
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14. Cardiomyopathy in cirrhosis: From pathophysiology to clinical careKey points
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Hongqun Liu, Jwan A. Naser, Grace Lin, and Samuel S. Lee
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cardiac ,cirrhosis ,hemodynamics ,MRI ,echocardiography ,prolonged QT Interval ,Diseases of the digestive system. Gastroenterology ,RC799-869 - Abstract
Summary: Cirrhotic cardiomyopathy (CCM) is defined as systolic or diastolic dysfunction in the absence of prior heart disease or another identifiable cause in patients with cirrhosis, in whom it is an important determinant of outcome. Its underlying pathogenic/pathophysiological mechanisms are rooted in two distinct pathways: 1) factors associated with portal hypertension, hyperdynamic circulation, gut bacterial/endotoxin translocation and the resultant inflammatory phenotype; 2) hepatocellular insufficiency with altered synthesis or metabolism of substances such as proteins, lipids, carbohydrates, bile acids and hormones. Different criteria have been proposed to diagnose CCM; the first in 2005 by the World Congress of Gastroenterology, and more recently in 2019 by the Cirrhotic Cardiomyopathy Consortium. These criteria mainly utilised echocardiographic evaluation, with the latter refining the evaluation of diastolic function and integrating global longitudinal strain into the evaluation of systolic function, an important addition since the haemodynamic changes that occur in advanced cirrhosis may lead to overestimation of systolic function by left ventricular ejection fraction. Advances in cardiac imaging, such as cardiac magnetic resonance imaging and the incorporation of an exercise challenge, may help further refine the diagnosis of CCM. Over recent years, CCM has been shown to contribute to increased mortality and morbidity after major interventions, such as liver transplantation and transjugular intrahepatic portosystemic shunt insertion, and to play a pathophysiologic role in the genesis of hepatorenal syndrome. In this review, we discuss the pathogenesis/pathophysiology of CCM, its clinical implications, and the role of cardiac imaging modalities including MRI. We also compare diagnostic criteria and review the potential diagnostic role of electrocardiographic QT prolongation. At present, no definitive medical therapy exists, but some promising potential treatment strategies for CCM are reviewed.
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- 2024
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15. A Dynamic Model for Predicting Outcome in Patients with HBV Related Acute-On-Chronic Liver Failure
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Wei Lin, Jing Zhang, Xiaohui Liu, Hongqun Liu, Jinqiu He, Ming Li, Shuqin Zhang, Hong Chen, Changqing Zhang, Wenfang Wu, Chenggang Jin, Samuel S. Lee, Zhongping Duan, and Yuexin Zhang
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Prognosis ,Hepatitis B ,Nucleoside analog ,Cirrhosis ,Specialties of internal medicine ,RC581-951 - Abstract
Introduction and aim. Accurately predicting the prognosis of individual patient is crucial in the management of ACLF. We aimed to establish a specific prognostic model for HBV-related ACLF patients treated with nucleoside analog (NA).Material and methods. We prospectively collected 205 ACLF cases diagnosed according to the APASL criteria. A dynamic prognostic model based on APASL criteria was established and validated. To demonstrate that the model is also applicable to those within EASL criteria, we divided the patients into two groups: met APASL criteria only (group A, n = 123); met both APASL and EASL criteria (group B, n = 82). Its prognostic accuracy was also compared with chronic liver failure-sequential organ failure assessment (CLIF-SOFA) score in group B.Results. The model is: R = 0.94 x Bilirubin + 0.53 x evolution of Bilirubin - 0.45 x PT-A - 0.22 x evolution in PT-A -0.1 x PLT + 10 x anti-HBe. The area under receiver operating characteristic curve (AUC) of the model for predicting 90-day mortality was 0.86, which was significantly higher than that of model for end stage liver disease(MELD), MELD-Na, CLIF-SOFA, ΔMELD (7d) and ΔMELD-Na (7d), ACLIF- SOFA(7d) (all p < 0.01). The AUC of our model in the validation group was 0.79 which was superior to MELD (0.45) CLIF-SOFA (0.53) score in group B patients (p < 0.01).Conclusion. In conclusion, the model was superior to the conventional methods in predicting the outcomes of patients with HBV related ACLF treated with NA. It is the first description of a novel prognostic model using consecutive data in patients with HBV-induced acute-on-chronic liver failure (ACLF) treated by nucleoside analogs.
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- 2018
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16. Long-Term Follow-up and Quantitative Hepatitis B Surface Antigen Monitoring in North American Chronic HBV Carriers
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Conar R. O’Neil, Stephen E. Congly, M. Sarah Rose, Samuel S. Lee, Meredith A. Borman, Carmen L. Charlton, Carla Osiowy, Mark G. Swain, Kelly W. Burak, and Carla S. Coffin
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Chronic Hepatitis B ,Natural History ,Disease Phase ,Nucleoside Analogues ,Diagnostic Test ,Canada ,Specialties of internal medicine ,RC581-951 - Abstract
Introduction. Quantitative hepatitis B surface antigen (qHBsAg) combined with HBV DNA may be useful for predicting chronic hepatitis B (CHB) activity and nucleoside analogue (NA) response.Material and methods. In this retrospective cohort study we evaluated qHBsAg levels according to CHB disease phase and among patients on treatment. Random effect logistic regression analysis was used to analyze qHBsAg change with time in the NA-treated cohort.Results. 545 CHB carriers [56% M, median age 48 y (IQR 38-59), 73% Asian] had qHBsAg testing. In the untreated group (44%), 8% were classified as immune tolerant, 10% immune clearance, 40% inactive, and 43% had HBeAg- CHB and the median HBsAg levels were 4.6 (IQR 3.4-4.9), 4.0 (IQR 3.4-4.5), 2.9 (IQR 1.4-3.8), and 3.2 log IU/mL (IQR 2.6-4.0), respectively; p < 0.001. In the NA-treated group (28% entecavir, 68% tenofovir, 4% lamivudine), no significant change in qHBsAg levels occured with time. However, 19% of patients on long-term NA had sustained qHBsAg < 2 log10 IU/mL.Conclusion. qHBsAg titers were associated with CHB phase and remained stable in those on long-term NA. A significant number of treated patients had low-level qHBsAg, of which some may be eligible for treatment discontinuation without risk of flare.
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- 2018
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17. Is pre-treatment liver biopsy necessary for all hepatitis C genotypes?
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Kevork M. Peltekian, Dr., Vincent G. Bain, Samuel S. Lee, Morris Sherman, Curtis L. Cooper, Eric M. Yoshida, Paul J. Marotta, Mel Krajden, Robert Balshaw, and Marc Deschênes
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Chronic hepatitis C ,Liver biopsy ,Outcomes research ,Practice guidelines ,Antiviral therapy ,Adherence ,Specialties of internal medicine ,RC581-951 - Abstract
Background. Current practice guidelines recommend liver biopsy prior to treatment of hepatitis C genotype-1 but not for genotype-2/3; this is based on expert opinion, not on published evidence. Methods. In retrospective analysis of a large trial database prior to the publication of recent guidelines, we compared outcomes in 985 treatment-naïve patients with hepatitis C who did or did not undergo liver biopsy before starting peginterferon alfa-2a plus ribavirin. Results. Physicians elected to treat 141/654 (21.6%) genotype-1 patients and 126/331 (38.1%) genotype-2/3 patients without liver biopsy. There were no differences in baseline characteristics among those with or without pre-treatment liver biopsy, except for female preponderance in genotype-1 patients with liver biopsy. The sustained viral response (SVR) rate was no different amongst genotype-2/3 patients who had a biopsy before treatment with 66.3% SVR vs. 69.8% of those treated without biopsy (p = 0.546), but significantly higher among genotype-1 patients with pre-treatment liver biopsy at 54.6 vs. 44.0% for those treated without a liver biopsy (p = 0.029). In genotype-1 patients with liver biopsy, more patients with cirrhosis had dose adjustments (p = 0.0057) rather than drug discontinuation. There was tendency for earlier discontinuation among patients without pre-treatment liver biopsy. Conclusions. Pre-treatment liver biopsy was associated with better SVR amongst genotype-1 patients. This improvement may reflect ongoing commitment to completing the treatment course by both patient and physician. In genotype-2/3 patients, pre-treatment liver biopsy may not be essential to maximize SVR rates. This study validates the recommendations of the most recent treatment guidelines for hepatitis C.
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- 2011
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18. TAVR-in-TAVR for Early Degeneration of a Novel Self-Expandable Valve Dedicated to Treatment of Aortic Regurgitation.
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Nienaber S, Curio J, Lee S, Mauri V, Dohr J, Baldus S, Kuhn E, Wienemann H, and Adam M
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Competing Interests: Funding Support and Author Disclosures Dr Curio has received research grant support from Boston Scientific. Dr Wienemann has received travel grants from JenaValve. Dr Adam has received personal fees from Abbott, JenaValve, Medtronic, and Meril. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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- 2024
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19. How Ophthalmologists Can Decarbonize Eye Care: A Review of Existing Sustainability Strategies and Steps Ophthalmologists Can Take.
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Sherry B, Lee S, Ramos Cadena MLA, Laynor G, Patel SR, Simon MD, Romanowski EG, Hochman SE, Schuman JS, Prescott C, and Thiel CL
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- Humans, Ophthalmologists, Cataract Extraction, Cataract, Lens, Crystalline, Ophthalmology
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Topic: Understanding approaches to sustainability in cataract surgery and their risks and benefits., Clinical Relevance: In the United States, health care is responsible for approximately 8.5% of greenhouse gas (GHG), and cataract surgery is one of the most commonly performed surgical procedures. Ophthalmologists can contribute to reducing GHG emissions, which lead to a steadily increasing list of health concerns ranging from trauma to food instability., Methods: We conducted a literature review to identify the benefits and risks of sustainability interventions. We then organized these interventions into a decision tree for use by individual surgeons., Results: Identified sustainability interventions fall into the domains of advocacy and education, pharmaceuticals, process, and supplies and waste. Existing literature shows certain interventions may be safe, cost-effective, and environmentally friendly. These include dispensing medications at home to patients after surgery, multi-dosing appropriate medications, training staff to properly sort medical waste, reducing the number of supplies used during surgery, and implementing immediate sequential bilateral cataract surgery where clinically appropriate. The literature was lacking on the benefits or risks for some interventions, such as switching specific single-use supplies to reusables or implementing a hub-and-spoke-style operating room setup. Many of the advocacy and education interventions have inadequate literature specific to ophthalmology but are likely to have minimal risks., Conclusions: Ophthalmologists can engage in a variety of safe and effective approaches to reduce or eliminate dangerous GHG emissions associated with cataract surgery., Financial Disclosure(s): Proprietary or commercial disclosure may be found after the references., (Copyright © 2023 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.)
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- 2023
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20. Preoperative Stress Test and Postoperative MI in Patients Requiring Lower Extremity Bypass for Critical Limb Ischemia.
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Lee S, Qato K, Conway A, Nguyen Tran N, Leung TM, Giangola G, and Carroccio A
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- Aged, Comorbidity, Critical Illness, Databases, Factual, Electrocardiography, Female, Hospital Mortality, Humans, Ischemia diagnostic imaging, Ischemia mortality, Limb Salvage, Male, Middle Aged, Myocardial Infarction diagnosis, Myocardial Infarction mortality, Myocardial Ischemia mortality, Peripheral Arterial Disease diagnostic imaging, Peripheral Arterial Disease mortality, Predictive Value of Tests, Retrospective Studies, Risk Assessment, Risk Factors, Time Factors, Treatment Outcome, Vascular Surgical Procedures mortality, Exercise Test, Ischemia surgery, Lower Extremity blood supply, Myocardial Infarction epidemiology, Myocardial Ischemia diagnosis, Peripheral Arterial Disease surgery, Vascular Surgical Procedures adverse effects
- Abstract
Background: Patients with critical limb ischemia (CLI) often require lower extremity bypass surgery for limb salvage. A myocardial infarction (MI) is a major postoperative risk. Our objective is to assess the utility of preoperative stress test in determining patient outcomes., Methods: This is a retrospective study utilizing the national Vascular Quality Initiative database. We collected data from 2013-2018 on all patients undergoing lower extremity bypass for CLI and assessed whether or not they had a preoperative stress test. Rates of an MI were then compared between groups of patients who either did not receive a stress test, had a normal stress test or a positive stress test. An MI was distinguished as troponin only and electrocardiogram (EKG)/clinical. Our secondary end point was in-hospital mortality. Univariate and multivariate analysis with the stress test as a covariate was used to determine significance., Results: During this time period, 29,937 bypasses were performed on 27,219 patients. The average age was 67.5 years (±11.09), 66.3% were men, and 17.3% were African American. Risk factors included hypertension (89.5%), diabetes (55.9%), congestive heart failure (20%), coronary artery disease (32.5%), coronary artery bypass graft (22.2%), and percutaneous coronary intervention (21%). 19,108 patients (64.1%) did not undergo the stress test before bypass, 6,830 (22.9%) had a normal stress test, and 2,898 (9.7%) had a positive stress test. Overall rate of an MI was 4%, with 2% being troponin only and 2% EKG/clinical. The positive stress test had a higher rate of troponin only (2.85%) as well as EKG/clinical (3.37%) MI. For every 10 year increase in age, the odds of having a postoperative MI increased by 27% (P < 0.0001). Overall in-hospital mortality was 1.4%. Patients with positive stress tests had a 2.6% mortality compared with normal/not performed at 1.3%. Of the patients who died, 21.5% had an EKG/clinical MI. Of those patients, 50% did not have a stress test, 12% had normal stress tests, and 23% had positive stress tests. When comparing rates of patients who died or had an MI, there was no difference between patients who had no or a normal stress test (7.29%) versus those who had a positive stress test (7.58%), (P = 0.11)., Conclusions: A positive stress test before lower extremity bypass is a significant predictor of a postoperative MI. However, mortality increase was minimal in patients with a positive stress test. Therefore, the stress test result should not delay care for patients needing urgent revascularization., (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Published
- 2021
- Full Text
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21. Risk Factors for Postoperative Hypotension and Hypertension following Carotid Endarterectomy.
- Author
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Lee S, Conway AM, Nguyen Tranh N, Anand G, Leung TM, Fatakhova O, Giangola G, and Carroccio A
- Subjects
- Aged, Aged, 80 and over, Antihypertensive Agents therapeutic use, Databases, Factual, Female, Humans, Hypertension diagnosis, Hypertension drug therapy, Hypertension physiopathology, Hypotension diagnosis, Hypotension drug therapy, Hypotension physiopathology, Male, Middle Aged, Retrospective Studies, Risk Assessment, Risk Factors, Time Factors, Treatment Outcome, Vasoconstrictor Agents therapeutic use, Blood Pressure drug effects, Endarterectomy, Carotid adverse effects, Hypertension etiology, Hypotension etiology
- Abstract
Background: Patients undergoing carotid endarterectomy (CEA) often experience postoperative hemodynamic changes that require intravenous medications for hypo- and hypertension. Prior studies have found these changes to be associated with increased risks of 30-day mortality, stroke, myocardial infarction (MI), and length of stay (LOS). Our aim is to investigate preoperative risk factors associated with the need for postoperative intravenous medications for blood pressure control., Methods: A retrospective review of an internally maintained prospective database of patients undergoing carotid interventions between January 2014 and March 2019 was performed. Demographic data, clinical history, and perioperative data were recorded. Carotid artery stents and reinterventions were excluded. Our primary end points were the need to intervene with intravenous medication for either postoperative hypotension [systolic blood pressure (SBP) <100 mm Hg] or postoperative hypertension (SBP >160 mm Hg)., Results: A total of 221 patients were included in the study after excluding those with a prior ipsilateral CEA or carotid artery stent. The mean age was 72.3 (±8.9) years, 157 (71%) patients were male, and 78 (35.3%) were Caucasian. Following CEA, 151 (68.3%) patients were normotensive, while 33 (14.9%) and 37 (16.7%) required medication for hypotension and hypertension, respectively. A univariate logistic regression identified 5 variables as being associated with postoperative blood pressure including race, history of MI, prior percutaneous transluminal coronary angioplasty (PTCA), statin use, and angiotensin-converting enzyme-inhibitor/angiotensin-receptor blocker (ARB) use. A stepwise regression selection found race, prior MI, and statin use to be associated with our primary end points. The hypertensive group was more likely to have a history of MI compared to the hypotensive and normotensive groups (40.5% vs. 27.3% vs. 18.5%, P = 0.02), PTCA (43.2% vs. 39.4% vs. 23.8%, P = 0.03), and statin use (94.6% vs. 93.9% vs. 78.8%, P = 0.01). Mean LOS was also the highest for the hypertensive group, followed by hypotensive and normotensive patients [2.0 (±1.6) vs. 1.8 (±2.4) vs. 1.3 (±0.8), P = 0.002]. Multivariable logistic regression demonstrated that non-Caucasian patients [odds ratio (OR) 2.72, 95% confidence interval (CI) 1.26-5.86, P = 0.01] and those with a history of MI (OR 2.98, 95% CI 1.33-6.67) were more likely to have postoperative hypertension compared to patients who were Caucasian or had no history of MI., Conclusions: Postoperative hypertension is associated with non-Caucasian race and a history of MI. Given the potential implications for adverse perioperative outcomes including MI, mortality, and LOS, it is important to continue to elucidate potential risk factors in order to further tailor the perioperative management of patients undergoing CEA., (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Published
- 2020
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22. Pseudotumor cerebri in a transgender woman: case report and literature review.
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Wang Y, McClelland C, Lee S, and Lee MS
- Subjects
- Female, Humans, Pseudotumor Cerebri, Transgender Persons
- Published
- 2020
- Full Text
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23. Factors predicting malignancy in adult intussusception: An experience in university-affiliated hospitals.
- Author
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Kim JW, Lee BH, Park SG, Kim BC, Lee S, and Lee SJ
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Colonic Neoplasms diagnosis, Female, Hospitals, University, Humans, Intussusception diagnosis, Male, Middle Aged, Retrospective Studies, Risk Factors, Young Adult, Colonic Neoplasms complications, Intussusception etiology
- Abstract
Background: Intussusception is one of the common causes of intestinal obstruction in children but is uncommon in adults. Unlike pediatric intussusception, most adult cases have a demonstrable etiology. The purpose of this study was to review our experience of adult intussusception and to identify the predictive factors for malignancy in this disease., Methods: We retrospectively reviewed the medical records of patients who were diagnosed with intussusception and admitted to the six Hallym University-affiliated hospitals between January 2005 and July 2016., Results: The 77 patients had a mean age of 50.5 years (range, 18-91 years). Enteric intussusception is the most common type of adult intussusception (33.7%), and 11 patients (14.2%) had no definite lesion at operation. The most common symptom was abdominal pain (90.9%), and 18 (23.3%) presented with chronic symptoms. Computed tomography was the most common diagnostic modality used, with a diagnostic accuracy of 96.9%. The leading point was identified in 62 (80.5%) patients. Malignancy was more frequently present in the colonic type than in the other two types (61.5% vs. 10%, 37.9%). In a multivariate analysis, chronic symptom >14 days (p = 0.031) and colonic intussusception (p = 0.026) were independent predictors for malignancy., Conclusions: Enteric intussusception is the most common type of adult intussusception, and the most common test is computed tomography. Because chronic symptoms and colonic-type intussusception were predictive factors for malignancy, en bloc resection should be considered in patients with chronic or colonic intussusception., (Copyright © 2017. Published by Elsevier Taiwan.)
- Published
- 2018
- Full Text
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24. Some Non-FDA Approved Uses for Neuromodulation in Treating Autonomic Nervous System Disorders: A Discussion of the Preliminary Support.
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Lee S and Abd-Elsayed A
- Subjects
- Clinical Trials as Topic statistics & numerical data, Deep Brain Stimulation, Humans, Autonomic Nervous System physiology, Autonomic Nervous System Diseases therapy, Electric Stimulation Therapy methods
- Abstract
Introduction: Neuromodulation, including cavernous nerve stimulation, gastric electrical stimulation, deep brain stimulation, and vagus nerve stimulation, has been used with success in treating several functional disease conditions. The FDA has approved the use of neuromodulation for a few indications. We discuss in our review article the evidence of using neuromodulation for treating some important disorders involving the autonomic nervous system that are not currently FDA approved., Methods: This was a review article that included a systematic online web search for human clinical studies testing the efficacy of neuromodulation in treating erectile dysfunction, gastroparesis, gastroesophageal reflux disease, obesity, asthma, and heart failure. Our review includes all feasibility studies, nonrandomized clinical trials, and randomized controlled trials., Results: Our systematic literature search found 3, 4, 5, 4, 1, and 4 clinical studies relating to erectile dysfunction, gastroparesis, gastroesophageal reflux disease, obesity, asthma, and heart failure, respectively., Conclusion: This review article shows preliminary support based on clinical studies that neuromodulation can be of benefit for patients with important autonomic nervous system disease conditions that are not currently approved by the FDA. All of these investigational uses are encouraging; further studies are necessary and warranted for all indications discussed in this review before achieving FDA approval., (© 2016 International Neuromodulation Society.)
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- 2016
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25. Genetic dissection of the tail suspension test: a mouse model of stress vulnerability and antidepressant response.
- Author
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Liu X, Stancliffe D, Lee S, Mathur S, and Gershenfeld HK
- Subjects
- Animals, Antidepressive Agents pharmacology, Behavior, Animal drug effects, Behavior, Animal physiology, Chromosomes, Mammalian genetics, Crosses, Genetic, Fever genetics, Genetic Predisposition to Disease genetics, Imipramine pharmacology, Imipramine therapeutic use, Immobilization physiology, Immobilization psychology, Immunohistochemistry, Injections, Intraperitoneal, Lod Score, Mice, Mice, Inbred Strains, Receptors, Cell Surface genetics, Receptors, GABA-A drug effects, Receptors, GABA-A genetics, Receptors, Leptin, Stress, Psychological etiology, Terminology as Topic, Antidepressive Agents therapeutic use, Chromosome Mapping, Disease Models, Animal, Hindlimb Suspension physiology, Quantitative Trait Loci genetics, Stress, Psychological drug therapy, Stress, Psychological genetics
- Abstract
Background: The tail suspension test (TST) is a mouse screening test for antidepressants., Methods: An F2 intercross was derived from NMRI and 129S6 inbred strains (n = 747). Mice underwent standardized TST with 2 sessions: (1) baseline and (2) imipramine (30 mg/kg, intraperitoneally) TST., Results: A whole genome scan of this intercross mapped significant basal TST quantitative trait loci (QTL) on chromosomes (chr) 5 (peak 61 cM, Lod 5.7), 12 (peak 43 cM, Lod 5.2), and 18 (peak 51 cM, Lod 3.0). A suggestive QTL on chr 4 (peak 62 cM; Lod 3.1) overlapped regions containing previously mapped QTLs. For TST imipramine response, QTL were mapped on chr 1, 4, and 5. The chromosome 5 locus affected basal TST, antidepressant immobility response, and tail suspension-induced hyperthermia (TSIH) behaviors. An outbred NMRI F2 population provided further evidence for a chr 5 QTL. This chr 5 region harbors a cluster of gamma aminobutyric acid (GABA)-A receptor subunits and the human syntenic region includes chr 4p, 1p11, 12q24, and 22q11.24. A significant TSIH QTL (Tsih1) mapped on chr 4 near the Leptin receptor (Lepr)., Conclusions: These QTL provide potential regions of interest for human genetic studies in stress-diathesis models of psychiatric illness and antidepressant responsiveness.
- Published
- 2007
- Full Text
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