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  1. Article ; Online: Effectiveness of Insole Colour on Impact Loading and Lower-Limb Kinematics When Running at Preferred and Nonpreferred Speeds.

    Wang, Yi / Lam, Wing-Kai / Pak, Lok-Yee / Wong, Charis K-W / Tan, Mohammad F / Leung, Aaron K-L

    Journal of healthcare engineering

    2021  Volume 2021, Page(s) 8947433

    Abstract: While colour of red can play a significant role in altering human perception and performances, little is known about its perceptual-motor effect on running mechanics. This study examined the effects of variations in insole colours on impact forces, ankle ...

    Abstract While colour of red can play a significant role in altering human perception and performances, little is known about its perceptual-motor effect on running mechanics. This study examined the effects of variations in insole colours on impact forces, ankle kinematics, and trial-to-trial reliability at various running speeds. Sixteen male recreational runners ran on instrumented treadmill at slow (90%), preferred (100%), and fast (110%) running speeds when wearing insoles in red, blue, and white colours. We used synchronized force platform and motion capturing system to measure ground reaction force, ankle sagittal and frontal kinematics, and movement variability. A two-way (colour x speed) ANOVA with repeated measures was performed with Bonferroni adjusted post hoc comparisons, with alpha set at 0.05. Data analyses indicated that participants demonstrated higher impact and maximum loading rate of ground reaction force, longer stride length, shorter contact time, and smaller touchdown ankle inversion as well as larger ankle sagittal range of motion (RoM), but smaller frontal RoM in fast speed as compared with preferred (
    MeSH term(s) Biomechanical Phenomena ; Color ; Humans ; Male ; Reproducibility of Results ; Running ; Shoes
    Language English
    Publishing date 2021-12-01
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2545054-2
    ISSN 2040-2309 ; 2040-2295
    ISSN (online) 2040-2309
    ISSN 2040-2295
    DOI 10.1155/2021/8947433
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Effectiveness of Insole Colour on Impact Loading and Lower-Limb Kinematics When Running at Preferred and Nonpreferred Speeds

    Yi Wang / Wing-Kai Lam / Lok-Yee Pak / Charis K.-W. Wong / Mohammad F. Tan / Aaron K.-L. Leung

    Journal of Healthcare Engineering, Vol

    2021  Volume 2021

    Abstract: While colour of red can play a significant role in altering human perception and performances, little is known about its perceptual-motor effect on running mechanics. This study examined the effects of variations in insole colours on impact forces, ankle ...

    Abstract While colour of red can play a significant role in altering human perception and performances, little is known about its perceptual-motor effect on running mechanics. This study examined the effects of variations in insole colours on impact forces, ankle kinematics, and trial-to-trial reliability at various running speeds. Sixteen male recreational runners ran on instrumented treadmill at slow (90%), preferred (100%), and fast (110%) running speeds when wearing insoles in red, blue, and white colours. We used synchronized force platform and motion capturing system to measure ground reaction force, ankle sagittal and frontal kinematics, and movement variability. A two-way (colour x speed) ANOVA with repeated measures was performed with Bonferroni adjusted post hoc comparisons, with alpha set at 0.05. Data analyses indicated that participants demonstrated higher impact and maximum loading rate of ground reaction force, longer stride length, shorter contact time, and smaller touchdown ankle inversion as well as larger ankle sagittal range of motion (RoM), but smaller frontal RoM in fast speed as compared with preferred P<0.05 and slow speeds P<0.001. Although insole colour had minimal effect on mean values of any tested variables P>0.05, participants wearing red-coloured orthoses showed higher coefficient of variation values for maximum loading rate than wearing blue insoles P=0.009. These results suggest that running at faster speed would lead to higher impact loading and altered lower-limb mechanics and that colour used on the tops of insoles influences the wearers’ movement repeatability, with implications for use of foot insole in running.
    Keywords Medicine (General) ; R5-920 ; Medical technology ; R855-855.5
    Subject code 796
    Language English
    Publishing date 2021-01-01T00:00:00Z
    Publisher Hindawi Limited
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Effectiveness and Reliability of Foot Orthoses on Impact Loading and Lower Limb Kinematics When Running at Preferred and Nonpreferred Speeds.

    Wang, Yi / Lam, Wing K / Wong, Charis K / Park, Lok Y / Tan, Mohammad F / Leung, Aaron K L

    Journal of applied biomechanics

    2020  Volume 37, Issue 1, Page(s) 66–73

    Abstract: This study examined the effect of foot orthoses used on ground reaction forces, ankle, and knee kinematics when running at preferred and nonpreferred speeds. Sixteen runners ran on instrumented treadmills at various speeds (90%, 100%, and 110% of ... ...

    Abstract This study examined the effect of foot orthoses used on ground reaction forces, ankle, and knee kinematics when running at preferred and nonpreferred speeds. Sixteen runners ran on instrumented treadmills at various speeds (90%, 100%, and 110% of preferred speed) when wearing arch-support and flat-control orthoses. Two-way repeated analysis of variance (ANOVA) was performed on the mean and coefficient of variation of all variables. Results indicated that arch-support orthoses experienced larger maximum loading rates than flat-control orthoses (P = .017, 95% CI, 2.22 to 19.53). Slower speed was related to smaller loading rates (preferred: P = .002, 95% CI, -17.02 to -4.20; faster: P = .003, 95% CI, -29.78 to -6.17), shorter stride length (preferred: P < .001, 95% CI, -0.204 to -0.090; faster: P < .001, 95% CI, -0.382 to -0.237), and longer contact time (preferred: P < .001, 95% CI, 0.006-0.021; faster: 95% CI, 0.012-0.042). In arch-support condition, preferred speed induced higher stride length coefficient of variation (P = .046, 95% CI, 0.035-1.117) than faster speed, while displaying no differences in flat-control condition. These findings suggest that the use of arch-support orthoses would influence impact loading, but not spatial-temporal and joint kinematics in recreational runners.
    MeSH term(s) Adult ; Ankle/physiology ; Biomechanical Phenomena ; Foot Orthoses ; Humans ; Knee/physiology ; Male ; Running/physiology ; Weight-Bearing ; Young Adult
    Language English
    Publishing date 2020-11-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1145288-2
    ISSN 1543-2688 ; 1065-8483
    ISSN (online) 1543-2688
    ISSN 1065-8483
    DOI 10.1123/jab.2019-0281
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Amino acid homeostasis is a target of metformin therapy.

    Forteath, Calum / Mordi, Ify / Nisr, Raid / Gutierrez-Lara, Erika J / Alqurashi, Noor / Phair, Iain R / Cameron, Amy R / Beall, Craig / Bahr, Ibrahim / Mohan, Mohapradeep / Wong, Aaron K F / Dihoum, Adel / Mohammad, Anwar / Palmer, Colin N A / Lamont, Douglas / Sakamoto, Kei / Viollet, Benoit / Foretz, Marc / Lang, Chim C /
    Rena, Graham

    Molecular metabolism

    2023  Volume 74, Page(s) 101750

    Abstract: Objective: Unexplained changes in regulation of branched chain amino acids (BCAA) during diabetes therapy with metformin have been known for years. Here we have investigated mechanisms underlying this effect.: Methods: We used cellular approaches, ... ...

    Abstract Objective: Unexplained changes in regulation of branched chain amino acids (BCAA) during diabetes therapy with metformin have been known for years. Here we have investigated mechanisms underlying this effect.
    Methods: We used cellular approaches, including single gene/protein measurements, as well as systems-level proteomics. Findings were then cross-validated with electronic health records and other data from human material.
    Results: In cell studies, we observed diminished uptake/incorporation of amino acids following metformin treatment of liver cells and cardiac myocytes. Supplementation of media with amino acids attenuated known effects of the drug, including on glucose production, providing a possible explanation for discrepancies between effective doses in vivo and in vitro observed in most studies. Data-Independent Acquisition proteomics identified that SNAT2, which mediates tertiary control of BCAA uptake, was the most strongly suppressed amino acid transporter in liver cells following metformin treatment. Other transporters were affected to a lesser extent. In humans, metformin attenuated increased risk of left ventricular hypertrophy due to the AA allele of KLF15, which is an inducer of BCAA catabolism. In plasma from a double-blind placebo-controlled trial in nondiabetic heart failure (trial registration: NCT00473876), metformin caused selective accumulation of plasma BCAA and glutamine, consistent with the effects in cells.
    Conclusions: Metformin restricts tertiary control of BCAA cellular uptake. We conclude that modulation of amino acid homeostasis contributes to therapeutic actions of the drug.
    MeSH term(s) Humans ; Metformin/pharmacology ; Metformin/therapeutic use ; Amino Acids, Branched-Chain/metabolism ; Amino Acids/metabolism ; Glucose ; Homeostasis
    Chemical Substances Metformin (9100L32L2N) ; Amino Acids, Branched-Chain ; Amino Acids ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2023-06-09
    Publishing country Germany
    Document type Randomized Controlled Trial ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2708735-9
    ISSN 2212-8778 ; 2212-8778
    ISSN (online) 2212-8778
    ISSN 2212-8778
    DOI 10.1016/j.molmet.2023.101750
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Travel-associated extensively drug-resistant typhoid fever: a case series to inform management in non-endemic regions.

    Posen, H Joshua / Wong, Waison / Farrar, Daniel S / Campigotto, Aaron / Chan, Tiffany / Barker, Kevin R / Hagmann, Stefan H F / Ryan, Edward T / LaRocque, Regina C / Earl, Ashlee M / Worby, Colin J / Castelli, Francesco / Fumadó, Victoria Pérez / Britton, Philip N / Libman, Michael / Hamer, Davidson H / Morris, Shaun K

    Journal of travel medicine

    2022  Volume 30, Issue 1

    Abstract: Background: Extensively drug-resistant (XDR) typhoid fever is a threat to travelers to Pakistan. We describe a multicontinental case series of travel-acquired XDR typhoid fever to demonstrate the global spread of the problem and encourage preventive ... ...

    Abstract Background: Extensively drug-resistant (XDR) typhoid fever is a threat to travelers to Pakistan. We describe a multicontinental case series of travel-acquired XDR typhoid fever to demonstrate the global spread of the problem and encourage preventive interventions as well as appropriate empiric antimicrobial use.
    Methods: Cases were extracted from the GeoSentinel database, microbiologic laboratory records of two large hospitals in Toronto, Canada, and by invitation to TropNet sites. All isolates were confirmed XDR Salmonella enterica serovar Typhi (Salmonella typhi), with resistance to ampicillin, ceftriaxone, ciprofloxacin and trimethoprim-sulfamethoxazole.
    Results: Seventeen cases were identified in Canada (10), USA (2), Spain (2), Italy (1), Australia (1) and Norway (1). Patients under 18 years represented 71% (12/17) of cases, and all patients travelled to Pakistan to visit friends or relatives. Only one patient is known to have been vaccinated. Predominant symptoms were fever, abdominal pain, vomiting and diarrhoea. Antimicrobial therapy was started on Day 1 of presentation in 75% (12/16) of patients, and transition to a carbapenem or azithromycin occurred a median of 2 days after blood culture was drawn. Antimicrobial susceptibilities were consistent with the XDR S. typhi phenotype, and whole genome sequencing on three isolates confirmed their belonging to the XDR variant of the H58 clade.
    Conclusions: XDR typhoid fever is a particular risk for travelers to Pakistan, and empiric use of a carbapenem or azithromycin should be considered. Pre-travel typhoid vaccination and counseling are necessary and urgent interventions, especially for visiting friends and relatives travelers. Ongoing sentinel surveillance of XDR typhoid fever is needed to understand changing epidemiology.
    MeSH term(s) Humans ; Typhoid Fever/epidemiology ; Travel ; Azithromycin ; Anti-Bacterial Agents ; Salmonella typhi ; Anti-Infective Agents ; Carbapenems ; Pakistan/epidemiology
    Chemical Substances Azithromycin (83905-01-5) ; Anti-Bacterial Agents ; Anti-Infective Agents ; Carbapenems
    Language English
    Publishing date 2022-07-31
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1212504-0
    ISSN 1708-8305 ; 1195-1982
    ISSN (online) 1708-8305
    ISSN 1195-1982
    DOI 10.1093/jtm/taac086
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  6. Article ; Online: Amino acid homeostasis is a target of metformin therapy

    Calum Forteath / Ify Mordi / Raid Nisr / Erika J. Gutierrez-Lara / Noor Alqurashi / Iain R. Phair / Amy R. Cameron / Craig Beall / Ibrahim Bahr / Mohapradeep Mohan / Aaron K.F. Wong / Adel Dihoum / Anwar Mohammad / Colin N.A. Palmer / Douglas Lamont / Kei Sakamoto / Benoit Viollet / Marc Foretz / Chim C. Lang /
    Graham Rena

    Molecular Metabolism, Vol 74, Iss , Pp 101750- (2023)

    2023  

    Abstract: Objective: Unexplained changes in regulation of branched chain amino acids (BCAA) during diabetes therapy with metformin have been known for years. Here we have investigated mechanisms underlying this effect. Methods: We used cellular approaches, ... ...

    Abstract Objective: Unexplained changes in regulation of branched chain amino acids (BCAA) during diabetes therapy with metformin have been known for years. Here we have investigated mechanisms underlying this effect. Methods: We used cellular approaches, including single gene/protein measurements, as well as systems-level proteomics. Findings were then cross-validated with electronic health records and other data from human material. Results: In cell studies, we observed diminished uptake/incorporation of amino acids following metformin treatment of liver cells and cardiac myocytes. Supplementation of media with amino acids attenuated known effects of the drug, including on glucose production, providing a possible explanation for discrepancies between effective doses in vivo and in vitro observed in most studies. Data-Independent Acquisition proteomics identified that SNAT2, which mediates tertiary control of BCAA uptake, was the most strongly suppressed amino acid transporter in liver cells following metformin treatment. Other transporters were affected to a lesser extent. In humans, metformin attenuated increased risk of left ventricular hypertrophy due to the AA allele of KLF15, which is an inducer of BCAA catabolism. In plasma from a double-blind placebo-controlled trial in nondiabetic heart failure (trial registration: NCT00473876), metformin caused selective accumulation of plasma BCAA and glutamine, consistent with the effects in cells. Conclusions: Metformin restricts tertiary control of BCAA cellular uptake. We conclude that modulation of amino acid homeostasis contributes to therapeutic actions of the drug.
    Keywords Metformin ; Branched chain amino acids ; mTOR ; SNAT2 ; Glutamine ; Rapamycin ; Internal medicine ; RC31-1245
    Language English
    Publishing date 2023-08-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article: Post-ST-Segment Elevation Myocardial Infarction Follow-Up Care During the COVID-19 Pandemic and the Possible Benefit of Telemedicine: An Observational Study.

    Zhang, Audrey A Y / Chew, Nicholas W S / Ng, Cheng Han / Phua, Kailun / Aye, Yin Nwe / Mai, Aaron / Kong, Gwyneth / Saw, Kalyar / Wong, Raymond C C / Kong, William K F / Poh, Kian-Keong / Chan, Koo-Hui / Low, Adrian Fatt-Hoe / Lee, Chi-Hang / Chan, Mark Yan-Yee / Chai, Ping / Yip, James / Yeo, Tiong-Cheng / Tan, Huay-Cheem /
    Loh, Poay-Huan

    Frontiers in cardiovascular medicine

    2021  Volume 8, Page(s) 755822

    Abstract: Background: ...

    Abstract Background:
    Language English
    Publishing date 2021-10-22
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2781496-8
    ISSN 2297-055X
    ISSN 2297-055X
    DOI 10.3389/fcvm.2021.755822
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  8. Article: Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood.

    Jakubek, Yasminka A / Ma, Xiaolong / Stilp, Adrienne M / Yu, Fulong / Bacon, Jason / Wong, Justin W / Aguet, Francois / Ardlie, Kristin / Arnett, Donna / Barnes, Kathleen / Bis, Joshua C / Blackwell, Tom / Becker, Lewis C / Boerwinkle, Eric / Bowler, Russell P / Budoff, Matthew J / Carson, April P / Chen, Jiawen / Cho, Michael H /
    Coresh, Josef / Cox, Nancy / de Vries, Paul S / DeMeo, Dawn L / Fardo, David W / Fornage, Myriam / Guo, Xiuqing / Hall, Michael E / Heard-Costa, Nancy / Hidalgo, Bertha / Irvin, Marguerite Ryan / Johnson, Andrew D / Kenny, Eimear E / Levy, Dan / Li, Yun / Lima, Joao Ac / Liu, Yongmei / Loos, Ruth J F / Machiela, Mitchell J / Mathias, Rasika A / Mitchell, Braxton D / Murabito, Joanne / Mychaleckyj, Josyf C / North, Kari / Orchard, Peter / Parker, Stephen Cj / Pershad, Yash / Peyser, Patricia A / Pratte, Katherine A / Psaty, Bruce M / Raffield, Laura M / Redline, Susan / Rich, Stephen S / Rotter, Jerome I / Shah, Sanjiv J / Smith, Jennifer A / Smith, Aaron P / Smith, Albert / Taub, Margaret / Tiwari, Hemant K / Tracy, Russell / Tuftin, Bjoernar / Bick, Alexander G / Sankaran, Vijay G / Reiner, Alexander P / Scheet, Paul / Auer, Paul L

    medRxiv : the preprint server for health sciences

    2024  

    Abstract: Mosaic loss of Y (mLOY) is the most common somatic chromosomal alteration detected in human blood. The presence of mLOY is associated with altered blood cell counts and increased risk of Alzheimer's disease, solid tumors, and other age-related diseases. ... ...

    Abstract Mosaic loss of Y (mLOY) is the most common somatic chromosomal alteration detected in human blood. The presence of mLOY is associated with altered blood cell counts and increased risk of Alzheimer's disease, solid tumors, and other age-related diseases. We sought to gain a better understanding of genetic drivers and associated phenotypes of mLOY through analyses of whole genome sequencing of a large set of genetically diverse males from the Trans-Omics for Precision Medicine (TOPMed) program. This approach enabled us to identify differences in mLOY frequencies across populations defined by genetic similarity, revealing a higher frequency of mLOY in the European American (EA) ancestry group compared to those of Hispanic American (HA), African American (AA), and East Asian (EAS) ancestry. Further, we identified two genes (
    Language English
    Publishing date 2024-04-19
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.04.16.24305851
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Reply: Meta-Analysis of the Index of Microvascular Resistance in Acute STEMI Using Incomplete Data.

    Bulluck, Heerajnarain / Foin, Nicolas / Cabrera-Fuentes, Hector A / Yeo, Khung K / Wong, Aaron S / Fam, Jiang M / Wong, Philip E / Tan, Jack W / Low, Adrian F / Hausenloy, Derek J

    JACC. Cardiovascular interventions

    2017  Volume 10, Issue 4, Page(s) 422

    MeSH term(s) Coronary Circulation ; Humans ; Percutaneous Coronary Intervention ; ST Elevation Myocardial Infarction
    Language English
    Publishing date 2017-02-23
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 2452157-7
    ISSN 1876-7605 ; 1936-8798
    ISSN (online) 1876-7605
    ISSN 1936-8798
    DOI 10.1016/j.jcin.2017.01.003
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  10. Article: Multi-MHz laser-scanning single-cell fluorescence microscopy by spatiotemporally encoded virtual source array.

    Wu, Jianglai / Tang, Anson H L / Mok, Aaron T Y / Yan, Wenwei / Chan, Godfrey C F / Wong, Kenneth K Y / Tsia, Kevin K

    Biomedical optics express

    2017  Volume 8, Issue 9, Page(s) 4160–4171

    Abstract: Apart from the spatial resolution enhancement, scaling of temporal resolution, equivalently the imaging throughput, of fluorescence microscopy is of equal importance in advancing cell biology and clinical diagnostics. Yet, this attribute has mostly been ... ...

    Abstract Apart from the spatial resolution enhancement, scaling of temporal resolution, equivalently the imaging throughput, of fluorescence microscopy is of equal importance in advancing cell biology and clinical diagnostics. Yet, this attribute has mostly been overlooked because of the inherent speed limitation of existing imaging strategies. To address the challenge, we employ an all-optical laser-scanning mechanism, enabled by an array of reconfigurable spatiotemporally-encoded virtual sources, to demonstrate ultrafast fluorescence microscopy at line-scan rate as high as 8 MHz. We show that this technique enables high-throughput single-cell microfluidic fluorescence imaging at 75,000 cells/second and high-speed cellular 2D dynamical imaging at 3,000 frames per second, outperforming the state-of-the-art high-speed cameras and the gold-standard laser scanning strategies. Together with its wide compatibility to the existing imaging modalities, this technology could empower new forms of high-throughput and high-speed biological fluorescence microscopy that was once challenged.
    Language English
    Publishing date 2017-08-21
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2572216-5
    ISSN 2156-7085
    ISSN 2156-7085
    DOI 10.1364/BOE.8.004160
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