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Institution

Taipei Veterans General Hospital

HealthcareTaipei, Taiwan
About: Taipei Veterans General Hospital is a healthcare organization based out in Taipei, Taiwan. It is known for research contribution in the topics: Population & Cancer. The organization has 11878 authors who have published 16478 publications receiving 363424 citations. The organization is also known as: Táiběi Róngmín Zǒngyī Yuàn.


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Journal ArticleDOI
TL;DR: In this paper, the authors investigated the risk of ischemic stroke and intracranial hemorrhage (ICH) and the net clinical benefit of OAC treatment for very elderly patients with atrial fibrillation (≥90 years of age).
Abstract: Background: Stroke prevention with oral anticoagulants (OACs) is the cornerstone for the management of atrial fibrillation (AF). However, data about the use of OACs among patients ≥90 years of age are limited. We aimed to investigate the risk of ischemic stroke and intracranial hemorrhage (ICH) and the net clinical benefit of OAC treatment for very elderly patients with AF (≥90 years of age). Methods: This study used the National Health Insurance Research Database in Taiwan. Risks of ischemic stroke and ICH were compared between 11 064 and 14 658 patients with and without AF ≥90 years of age without antithrombotic therapy from 1996 to 2011. Patients with AF (n=15 756) were divided into 3 groups (no treatment, antiplatelet agents, and warfarin), and the risks of stroke and ICH were analyzed. The risks of ischemic stroke and ICH were further compared between patients treated with warfarin and nonvitamin K antagonist OACs (NOACs) from 2012 to 2015 when NOACs were available in Taiwan. Results: Compared with patients without AF, patients with AF had an increased risk of ischemic stroke (event number/patient number, incidence = 742/11 064, 5.75%/y versus 1399/14 658, 3.00%/y; hazard ratio, 1.93; 95% confidence interval, 1.74–2.14) and similar risk of ICH (131/11 064, 0.97%/y versus 206/14 658, 0.54%/y; hazard ratio, 0.85; 95% confidence interval, 0.66–1.09) in competing risk analysis for mortality. Among patients with AF, warfarin use was associated with a lower stroke risk (39/617, 3.83%/y versus 742/11 064, 5.75%/y; hazard ratio, 0.69; 95% confidence interval, 0.49–0.96 in a competing risk model), with no difference in ICH risk compared with nontreatment. When compared with no antithrombotic therapy or antiplatelet drugs, warfarin was associated with a positive net clinical benefit. These findings persisted in propensity-matched analyses. Compared with warfarin, NOACs were associated with a lower risk of ICH (4/978, 0.42%/y versus 19/768, 1.63%/y; hazard ratio, 0.32; 95% confidence interval, 0.10–0.97 in a competing risk model), with no difference in risk of ischemic stroke. Conclusions: Among patients with AF ≥90 years of age, warfarin was associated with a lower risk of ischemic stroke and positive net clinical benefit. Compared with warfarin, NOACs were associated with a lower risk of ICH. Thus, OACs may still be considered as thromboprophylaxis for elderly patients, with NOACs being the more favorable choice.

176 citations

Journal ArticleDOI
Wanqing Wen1, Wei Zheng1, Yukinori Okada2, Fumihiko Takeuchi, Yasuharu Tabara3, Joo-Yeon Hwang, Rajkumar Dorajoo4, Huaixing Li5, Fuu Jen Tsai6, Xiaobo Yang7, Jiang He8, Ying Wu9, Meian He10, Yi Zhang11, Jun Liang12, Xiuqing Guo13, Wayne Huey-Herng Sheu14, Ryan J. Delahanty1, Xingyi Guo1, Michiaki Kubo, Ken Yamamoto15, Takayoshi Ohkubo16, Min Jin Go, Jianjun Liu4, Wei Gan5, Ching-Chu Chen17, Yong Gao7, Shengxu Li8, Nanette R. Lee18, Chen Wu19, Xueya Zhou20, Huai-Dong Song11, Jie Yao13, I-Te Lee21, Jirong Long1, Tatsuhiko Tsunoda, Koichi Akiyama, Naoyuki Takashima16, Yoon Shin Cho22, Rick Th Ong4, Ling Lu5, Chien-Hsiun Chen23, Aihua Tan7, Treva Rice24, Linda S. Adair9, Lixuan Gui10, Matthew A. Allison, Wen-Jane Lee25, Qiuyin Cai1, Minoru Isomura26, Satoshi Umemura27, Young-Jin Kim, Mark Seielstad28, James E. Hixson29, Yong-Bing Xiang11, Masato Isono, Bong-Jo Kim, Xueling Sim30, Wei Lu31, Toru Nabika26, Juyoung Lee, Wei-Yen Lim, Yu-Tang Gao11, Ryoichi Takayanagi15, Daehee Kang32, Tien Yin Wong33, Chao A. Hsiung34, I-Chien Wu34, Jyh-Ming Jimmy Juang35, Jiajun Shi1, Bo Youl Choi36, Tin Aung33, Frank B. Hu37, Mi Kyung Kim36, Wei-Yen Lim, Tzung-Dao Wang35, Min-Ho Shin38, Jeannette Lee, Bu-Tian Ji, Young-Hoon Lee39, Terri L. Young30, Dong Hoon Shin40, Byung-Yeol Chun41, Myeong Chan Cho, Bok-Ghee Han, Chii-Min Hwu42, Themistocles L. Assimes43, Devin Absher, Xiaofei Yan13, Eric Kim13, Jane Z. Kuo44, Soonil Kwon13, Kent D. Taylor13, Yii-Der Ida Chen13, Jerome I. Rotter13, Lu Qi37, Dingliang Zhu11, Tangchun Wu10, Karen L. Mohlke9, Dongfeng Gu19, Zengnan Mo7, Jer-Yuarn Wu23, Xu Lin5, Tetsuro Miki45, E. Shyong Tai30, Jong-Young Lee, Norihiro Kato, Xiao-Ou Shu1, Toshihiro Tanaka2 
TL;DR: A meta-analysis of associations between BMI and ∼2.5 million genotyped or imputed single nucleotide polymorphisms among 86 757 individuals of Asian ancestry, followed by in silico and de novo replication among 7488-47 352 additional Asian-ancestry individuals finds the association of BMI with rs2237892, rs671 and rs12229654 was significantly stronger among men than among women.
Abstract: Recent genetic association studies have identified 55 genetic loci associated with obesity or body mass index (BMI). The vast majority, 51 loci, however, were identified in European-ancestry populations. We conducted a meta-analysis of associations between BMI and ∼2.5 million genotyped or imputed single nucleotide polymorphisms among 86 757 individuals of Asian ancestry, followed by in silico and de novo replication among 7488-47 352 additional Asian-ancestry individuals. We identified four novel BMI-associated loci near the KCNQ1 (rs2237892, P = 9.29 × 10(-13)), ALDH2/MYL2 (rs671, P = 3.40 × 10(-11); rs12229654, P = 4.56 × 10(-9)), ITIH4 (rs2535633, P = 1.77 × 10(-10)) and NT5C2 (rs11191580, P = 3.83 × 10(-8)) genes. The association of BMI with rs2237892, rs671 and rs12229654 was significantly stronger among men than among women. Of the 51 BMI-associated loci initially identified in European-ancestry populations, we confirmed eight loci at the genome-wide significance level (P < 5.0 × 10(-8)) and an additional 14 at P < 1.0 × 10(-3) with the same direction of effect as reported previously. Findings from this analysis expand our knowledge of the genetic basis of obesity.

176 citations

Journal ArticleDOI
TL;DR: The results demonstrate that the development of suicidal behaviors in major depression is related to widespread but discrete volume reduction in several cortical and subcortical structures, fitting with the hypothesis that decreased cerebral volume in certain regions renders biological susceptibility to attempt suicide during depressive states.
Abstract: Late-onset major depression is thought to have a biological (vascular) basis, which could be a result of brain structure change. Vascular lesions can affect both the gray matter (GM) and white matter (WM), while most previous studies addressed WM abnormality. This study explored the disease- and symptom (history of suicide attempt) -related GM morphometry in elderly male patients with late-onset depression. A total of 70 patients with depression admitted to our geriatric psychiatric ward were investigated, and 26 age-matched males were recruited as controls. We used T1-weighted magnetic resonance imaging (MRI) to obtain cerebral structural information and adopted voxel-based morphometry (VBM) to investigate brain volume change related to disease (depression vs control) and symptom (depression with history of suicide attempt vs depression without history of suicide attempt). Late-onset depression was associated with smaller volumes in several regions of GM (insula and the posterior cingulate region) and WM (subcallosal cingulate cortex, floor of lateral ventricles, parahippocampal region, insula, and the cerebellum). Compared with nonsuicidal counterpart, suicidal depression was associated with decreased GM and WM volume in the frontal, parietal, and temporal regions, and the insula, lentiform nucleus, midbrain, and the cerebellum. Marked regional volume reduction was noticed at dorsal medial prefrontal cortex. Our results demonstrate that the development of suicidal behaviors in major depression is related to widespread but discrete volume reduction in several cortical and subcortical structures, fitting with the hypothesis that decreased cerebral volume in certain regions renders biological susceptibility to attempt suicide during depressive states.

176 citations

Journal ArticleDOI
TL;DR: In this article, a study was conducted to determine whether poor glycemic control contributes to the development of capsular serotype K1 or K2 Klebsiella pneumoniae liver abscess.
Abstract: Context: Diabetes mellitus (DM) and capsular serotypes K1 and K2 Klebsiella pneumoniae have been identified as risk factors for liver abscess and complicated endophthalmitis. Objective: The objective of this study was to determine whether poor glycemic control contributes to the development of capsular serotype K1 or K2 K. pneumoniae liver abscess. Design and Setting: Neutrophil phagocytosis in patients with type 2 DM and nondiabetic controls was compared with isolates from liver abscess. Phagocytic rates of 18 K1/K2 and nine non-K1/K2 K. pneumoniae strains were evaluated by flow cytometry and electron microscopy. Patients or Study Participants: Forty patients with type 2 diabetes, 14 with good glycemic control, 26 with poor glycemic control, and 13 age-matched healthy normal subjects, were studied. Main Outcome Measures: Phagocytic rate of K. pneumoniae was measured. Results: Phagocytosis of serotype K1/K2 isolates by neutrophils from diabetics was significantly less than normal controls (P < 0.01). Furt...

175 citations

Journal ArticleDOI
Jonathon Torchia1, Brian Golbourn1, Shengrui Feng2, Shengrui Feng1, King Ching Ho1, Patrick Sin-Chan1, Alexandre Vasiljevic, Joseph D. Norman1, Paul Guilhamon2, Livia Garzia1, Natalia R. Agamez1, Mei Lu1, Tiffany Chan1, Daniel Picard1, Pasqualino De Antonellis1, Dong Anh Khuong-Quang3, Aline Cristiane Planello2, Constanze Zeller2, Dalia Barsyte-Lovejoy2, Lucie Lafay-Cousin4, Louis Letourneau3, Mathieu Bourgey3, Man Yu, Deena M.A. Gendoo1, Misko Dzamba1, Mark Barszczyk, Tiago Medina2, Alexandra N. Riemenschneider1, A. Sorana Morrissy1, Young Shin Ra5, Vijay Ramaswamy1, Marc Remke1, Christopher Dunham6, Stephen Yip6, Ho Keung Ng7, Jian Qiang Lu8, Vivek Mehta8, Steffen Albrecht3, José Pimentel, Jennifer A. Chan9, Gino R. Somers, Claudia C. Faria, Lúcia Roque, Maryam Fouladi10, Lindsey M. Hoffman11, Andrew S. Moore12, Yin Wang13, Seung Ah Choi14, Jordan R. Hansford15, Daniel Catchpoole16, Diane K. Birks11, Nicholas K. Foreman11, Doug Strother8, Almos Klekner17, László Bognár17, Miklós Garami18, Peter Hauser18, Tibor Hortobágyi19, Beverly Wilson8, Juliette Hukin6, Anne Sophie Carret20, Timothy E. Van Meter21, Eugene Hwang22, Amar Gajjar23, Shih Hwa Chiou24, Hideo Nakamura25, Helen Toledano, Iris Fried26, Daniel W. Fults27, Takafumi Wataya28, Chris Fryer6, David D. Eisenstat8, Katrin Scheinemann29, Adam Fleming29, Donna L. Johnston30, Jean Michaud30, Shayna Zelcer28, Robert Hammond31, Samina Afzal32, David A. Ramsay31, Nongnuch Sirachainan33, Suradej Hongeng33, Noppadol Larbcharoensub33, Richard Grundy34, Rishi Lulla35, Jason Fangusaro35, Harriet Druker, Ute Bartels, Ronald Grant, David Malkin1, C. Jane McGlade1, Theodore Nicolaides36, Tarik Tihan36, Joanna J. Phillips36, Jacek Majewski3, Alexandre Montpetit3, Guillaume Bourque3, Gary D. Bader1, Alyssa Reddy37, G. Yancey Gillespie37, Monika Warmuth-Metz38, Stefan Rutkowski39, Uri Tabori1, Mathieu Lupien1, Mathieu Lupien2, Michael Brudno1, Ulrich Schüller39, Torsten Pietsch40, Alexander R. Judkins41, Cynthia Hawkins1, Eric Bouffet1, Seung-Ki Kim14, Peter B. Dirks1, Michael D. Taylor1, Anat Erdreich-Epstein42, Cheryl H. Arrowsmith2, Daniel D. De Carvalho2, Daniel D. De Carvalho1, James T. Rutka1, Nada Jabado3, Annie Huang1 
TL;DR: It is discovered that differential methylation of a PDGFRB-associated enhancer confers specific sensitivity of group 2 ATRT cells to dasatinib and nilotinib, and it is suggested that these are promising therapies for this highly lethal ATRT subtype.

175 citations


Authors

Showing all 11952 results

NameH-indexPapersCitations
Peng Huang9559039098
Hui Y. Lan8624823383
Yau-Huei Wei7838522286
Chunyu Liu7645026738
Ching-Yu Cheng7554139780
Shou-Dong Lee7578826066
Shih Ann Chen7369828441
Shuu Jiun Wang7150224800
Pesus Chou6548116907
Jong Ling Fuh6538319559
Shing Jong Lin6340113236
Charles Y. Chiu6223613185
Bor-Luen Chiang6046013597
Tzeng Ji Chen6054113644
Shih Hwa Chiou5826212289
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202321
2022111
20211,447
20201,267
20191,115
2018935