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  1. Article: Detection and Distribution of Viruses Infecting Garlic Crops in Australia.

    Cremer, Julia / Campbell, Paul / Steele, Visnja / Persley, Denis / Thomas, John / Harper, Stephen / Gambley, Cherie

    Plants (Basel, Switzerland)

    2021  Volume 10, Issue 5

    Abstract: The distribution of viruses in eastern Australian field garlic was evaluated. Detection assays were developed that involved generic RT-PCR for viruses in ... ...

    Abstract The distribution of viruses in eastern Australian field garlic was evaluated. Detection assays were developed that involved generic RT-PCR for viruses in the
    Language English
    Publishing date 2021-05-19
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2704341-1
    ISSN 2223-7747
    ISSN 2223-7747
    DOI 10.3390/plants10051013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Detection and Distribution of Viruses Infecting Garlic Crops in Australia

    Cremer, Julia / Campbell, Paul / Steele, Visnja / Persley, Denis / Thomas, John / Harper, Stephen / Gambley, Cherie

    Plants. 2021 May 19, v. 10, no. 5

    2021  

    Abstract: The distribution of viruses in eastern Australian field garlic was evaluated. Detection assays were developed that involved generic RT-PCR for viruses in the Allexivirus, Carlavirus and Potyvirus genera followed by virus-specific colorimetric dot-blot ... ...

    Abstract The distribution of viruses in eastern Australian field garlic was evaluated. Detection assays were developed that involved generic RT-PCR for viruses in the Allexivirus, Carlavirus and Potyvirus genera followed by virus-specific colorimetric dot-blot hybridization. Assays targeted the potyviruses (onion yellow dwarf virus (OYDV), shallot yellow stripe virus (SYSV), and leek yellow stripe virus (LYSV)), the carlaviruses (garlic common latent virus (GCLV) and shallot latent virus (SLV)), and the allexiviruses (garlic viruses A, B, C, X (GarVA, -B, -C, -X) and shallot virus X (ShVX)). Virus incidence in crops was consistently high, with most plants infected with at least one virus from each genus. OYDV, LYSV, SLV, and GCLV were commonly detected. Three of the four allexiviruses were in all districts surveyed but varied in incidence, whereas ShVX and SYSV were not detected. There was no association between virus species complement and bulb size, indicating size is not a good predictor of the virus status of planting material. The variation of virus incidence across different Australian growing districts and in different cultivars implies multiple introductions of viruses rather than spread within the country. The genetic diversity observed within coat protein sequences of some virus species also supports multiple separate introductions.
    Keywords Garlic common latent virus ; Leek yellow stripe virus ; Onion yellow dwarf virus ; Shallot latent virus ; Shallot yellow stripe virus ; bulbs ; coat proteins ; colorimetry ; cultivars ; garlic ; genetic variation ; nucleic acid hybridization ; viruses ; Australia
    Language English
    Dates of publication 2021-0519
    Publishing place Multidisciplinary Digital Publishing Institute
    Document type Article
    Note NAL-AP-2-clean
    ZDB-ID 2704341-1
    ISSN 2223-7747
    ISSN 2223-7747
    DOI 10.3390/plants10051013
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: Initial high-resolution microscopic mapping of active and inactive regulatory sequences proves non-random 3D arrangements in chromatin domain clusters.

    Cremer, Marion / Schmid, Volker J / Kraus, Felix / Markaki, Yolanda / Hellmann, Ines / Maiser, Andreas / Leonhardt, Heinrich / John, Sam / Stamatoyannopoulos, John / Cremer, Thomas

    Epigenetics & chromatin

    2017  Volume 10, Issue 1, Page(s) 39

    Abstract: Background: The association of active transcription regulatory elements (TREs) with DNAse I hypersensitivity (DHS[+]) and an 'open' local chromatin configuration has long been known. However, the 3D topography of TREs within the nuclear landscape of ... ...

    Abstract Background: The association of active transcription regulatory elements (TREs) with DNAse I hypersensitivity (DHS[+]) and an 'open' local chromatin configuration has long been known. However, the 3D topography of TREs within the nuclear landscape of individual cells in relation to their active or inactive status has remained elusive. Here, we explored the 3D nuclear topography of active and inactive TREs in the context of a recently proposed model for a functionally defined nuclear architecture, where an active and an inactive nuclear compartment (ANC-INC) form two spatially co-aligned and functionally interacting networks.
    Results: Using 3D structured illumination microscopy, we performed 3D FISH with differently labeled DNA probe sets targeting either sites with DHS[+], apparently active TREs, or DHS[-] sites harboring inactive TREs. Using an in-house image analysis tool, DNA targets were quantitatively mapped on chromatin compaction shaped 3D nuclear landscapes. Our analyses present evidence for a radial 3D organization of chromatin domain clusters (CDCs) with layers of increasing chromatin compaction from the periphery to the CDC core. Segments harboring active TREs are significantly enriched at the decondensed periphery of CDCs with loops penetrating into interchromatin compartment channels, constituting the ANC. In contrast, segments lacking active TREs (DHS[-]) are enriched toward the compacted interior of CDCs (INC).
    Conclusions: Our results add further evidence in support of the ANC-INC network model. The different 3D topographies of DHS[+] and DHS[-] sites suggest positional changes of TREs between the ANC and INC depending on their functional state, which might provide additional protection against an inappropriate activation. Our finding of a structural organization of CDCs based on radially arranged layers of different chromatin compaction levels indicates a complex higher-order chromatin organization beyond a dichotomic classification of chromatin into an 'open,' active and 'closed,' inactive state.
    Language English
    Publishing date 2017-08-07
    Publishing country England
    Document type Journal Article
    ZDB-ID 2462129-8
    ISSN 1756-8935 ; 1756-8935
    ISSN (online) 1756-8935
    ISSN 1756-8935
    DOI 10.1186/s13072-017-0146-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Francisella Subverts Innate Immune Signaling: Focus On PI3K/Akt.

    Cremer, Thomas John / Butchar, Jonathan P / Tridandapani, Susheela

    Frontiers in microbiology

    2011  Volume 5, Page(s) 13

    Abstract: Intracellular bacterial pathogens exploit host cells as a part of their lifecycle, and they do so by manipulating host cell signaling events. Many such bacteria are known to produce effector proteins that promote cell invasion, alter membrane trafficking, ...

    Abstract Intracellular bacterial pathogens exploit host cells as a part of their lifecycle, and they do so by manipulating host cell signaling events. Many such bacteria are known to produce effector proteins that promote cell invasion, alter membrane trafficking, and disrupt signaling cascades. This review highlights recent advances in our understanding of signaling pathways involved in host cell responses to Francisella tularensis, a facultative Gram-negative intracellular pathogen that causes tularemia. We highlight several key pathways that are targeted by Francisella, with a focus on the phosphatidylinositol 3-kinase/Akt pathway. Lastly, we discuss the emerging role of microRNAs (miRs), specifically miR-155, as a key regulator of host signaling and defense.
    Language English
    Publishing date 2011-02-07
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587354-4
    ISSN 1664-302X ; 1664-302X
    ISSN (online) 1664-302X
    ISSN 1664-302X
    DOI 10.3389/fmicb.2011.00013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Hematopoietic Deficiency of the Long Noncoding RNA MALAT1 Promotes Atherosclerosis and Plaque Inflammation.

    Cremer, Sebastian / Michalik, Katharina M / Fischer, Ariane / Pfisterer, Larissa / Jaé, Nicolas / Winter, Carla / Boon, Reinier A / Muhly-Reinholz, Marion / John, David / Uchida, Shizuka / Weber, Christian / Poller, Wolfgang / Günther, Stefan / Braun, Thomas / Li, Daniel Y / Maegdefessel, Lars / Perisic Matic, Ljubica / Hedin, Ulf / Soehnlein, Oliver /
    Zeiher, Andreas / Dimmeler, Stefanie

    Circulation

    2019  Volume 139, Issue 10, Page(s) 1320–1334

    Abstract: Background: The majority of the human genome comprises noncoding sequences, which are in part transcribed as long noncoding RNAs (lncRNAs). lncRNAs exhibit multiple functions, including the epigenetic control of gene expression. In this study, the ... ...

    Abstract Background: The majority of the human genome comprises noncoding sequences, which are in part transcribed as long noncoding RNAs (lncRNAs). lncRNAs exhibit multiple functions, including the epigenetic control of gene expression. In this study, the effect of the lncRNA MALAT1 (metastasis-associated lung adenocarcinoma transcript 1) on atherosclerosis was examined.
    Methods: The effect of MALAT1 on atherosclerosis was determined in apolipoprotein E-deficient (Apoe
    Results: Apoe
    Conclusions: Reduced levels of MALAT1 augment atherosclerotic lesion formation in mice and are associated with human atherosclerotic disease. The proatherosclerotic effects observed in Malat1
    MeSH term(s) Animals ; Aorta/metabolism ; Aorta/pathology ; Aortitis/genetics ; Aortitis/metabolism ; Aortitis/pathology ; Atherosclerosis/genetics ; Atherosclerosis/metabolism ; Atherosclerosis/pathology ; Bone Marrow Cells/metabolism ; Bone Marrow Cells/pathology ; Bone Marrow Transplantation ; Case-Control Studies ; Disease Models, Animal ; Down-Regulation ; Hematopoiesis ; Humans ; Mice, Inbred C57BL ; Mice, Knockout, ApoE ; MicroRNAs/genetics ; MicroRNAs/metabolism ; Plaque, Atherosclerotic ; RNA, Long Noncoding/genetics ; RNA, Long Noncoding/metabolism ; Signal Transduction
    Chemical Substances MALAT1 long non-coding RNA, human ; Malat1 long non-coding RNA, mouse ; MicroRNAs ; Mirn503 microRNA, mouse ; RNA, Long Noncoding
    Language English
    Publishing date 2019-01-20
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80099-5
    ISSN 1524-4539 ; 0009-7322 ; 0069-4193 ; 0065-8499
    ISSN (online) 1524-4539
    ISSN 0009-7322 ; 0069-4193 ; 0065-8499
    DOI 10.1161/CIRCULATIONAHA.117.029015
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Resistance Mechanisms to SYK Inhibition in Acute Myeloid Leukemia.

    Cremer, Anjali / Ellegast, Jana M / Alexe, Gabriela / Frank, Elizabeth S / Ross, Linda / Chu, S Haihua / Pikman, Yana / Robichaud, Amanda / Goodale, Amy / Häupl, Björn / Mohr, Sebastian / Rao, Arati V / Walker, Alison R / Blachly, James S / Piccioni, Federica / Armstrong, Scott A / Byrd, John C / Oellerich, Thomas / Stegmaier, Kimberly

    Cancer discovery

    2019  Volume 10, Issue 2, Page(s) 214–231

    Abstract: Spleen tyrosine kinase (SYK) is a nonmutated therapeutic target in acute myeloid leukemia (AML). Attempts to exploit SYK therapeutically in AML have shown promising results in combination with chemotherapy, likely reflecting induced mechanisms of ... ...

    Abstract Spleen tyrosine kinase (SYK) is a nonmutated therapeutic target in acute myeloid leukemia (AML). Attempts to exploit SYK therapeutically in AML have shown promising results in combination with chemotherapy, likely reflecting induced mechanisms of resistance to single-agent treatment
    MeSH term(s) Animals ; Antineoplastic Combined Chemotherapy Protocols/pharmacology ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Benzamides/pharmacology ; Benzamides/therapeutic use ; Cell Line, Tumor ; Clinical Trials, Phase I as Topic ; Clinical Trials, Phase II as Topic ; Diphenylamine/analogs & derivatives ; Diphenylamine/pharmacology ; Diphenylamine/therapeutic use ; Drug Resistance, Neoplasm/drug effects ; Drug Resistance, Neoplasm/genetics ; Drug Synergism ; Female ; Gene Expression Regulation, Leukemic/drug effects ; Humans ; Indazoles/pharmacology ; Indazoles/therapeutic use ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/genetics ; MAP Kinase Signaling System/drug effects ; MAP Kinase Signaling System/genetics ; Mice ; Mitogen-Activated Protein Kinase 1/genetics ; Mitogen-Activated Protein Kinase 1/metabolism ; Mitogen-Activated Protein Kinase Kinases/antagonists & inhibitors ; Mitogen-Activated Protein Kinase Kinases/metabolism ; Mutagenesis, Site-Directed ; Mutation ; Open Reading Frames/genetics ; Primary Cell Culture ; Protein Kinase Inhibitors/pharmacology ; Protein Kinase Inhibitors/therapeutic use ; Protein Tyrosine Phosphatase, Non-Receptor Type 11/genetics ; Protein Tyrosine Phosphatase, Non-Receptor Type 11/metabolism ; Pyrazines/pharmacology ; Pyrazines/therapeutic use ; Syk Kinase/antagonists & inhibitors ; Syk Kinase/metabolism ; Xenograft Model Antitumor Assays
    Chemical Substances 6-(1H-indazol-6-yl)-N-(4-morpholinophenyl)imidazo(1,2-a)pyrazin-8-amine ; Benzamides ; Indazoles ; Protein Kinase Inhibitors ; Pyrazines ; mirdametinib (86K0J5AK6M) ; Diphenylamine (9N3CBB0BIQ) ; SYK protein, human (EC 2.7.10.2) ; Syk Kinase (EC 2.7.10.2) ; MAPK1 protein, human (EC 2.7.11.24) ; Mitogen-Activated Protein Kinase 1 (EC 2.7.11.24) ; Mitogen-Activated Protein Kinase Kinases (EC 2.7.12.2) ; PTPN11 protein, human (EC 3.1.3.48) ; Protein Tyrosine Phosphatase, Non-Receptor Type 11 (EC 3.1.3.48)
    Language English
    Publishing date 2019-11-26
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2625242-9
    ISSN 2159-8290 ; 2159-8274
    ISSN (online) 2159-8290
    ISSN 2159-8274
    DOI 10.1158/2159-8290.CD-19-0209
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Francisella gains a survival advantage within mononuclear phagocytes by suppressing the host IFNgamma response.

    Parsa, Kishore V L / Butchar, Jonathan P / Rajaram, Murugesan V S / Cremer, Thomas J / Gunn, John S / Schlesinger, Larry S / Tridandapani, Susheela

    Molecular immunology

    2008  Volume 45, Issue 12, Page(s) 3428–3437

    Abstract: Tularemia is a zoonotic disease caused by the Gram-negative intracellular pathogen Francisella tularensis. These bacteria evade phagolysosomal fusion, escape from the phagosome and replicate in the host cell cytoplasm. IFNgamma has been shown to suppress ...

    Abstract Tularemia is a zoonotic disease caused by the Gram-negative intracellular pathogen Francisella tularensis. These bacteria evade phagolysosomal fusion, escape from the phagosome and replicate in the host cell cytoplasm. IFNgamma has been shown to suppress the intra-macrophage growth of Francisella through both nitric oxide-dependent and -independent pathways. Since Francisella is known to subvert host immune responses, we hypothesized that this pathogen could interfere with IFNgamma signaling. Here, we report that infection with Francisella suppresses IFNgamma-induced STAT1 expression and phosphorylation in both human and murine mononuclear phagocytes. This suppressive effect of Francisella is independent of phagosomal escape or replication and is mediated by a heat-stable and constitutively expressed bacterial factor. An analysis of the molecular mechanism of STAT1 inhibition indicated that expression of SOCS3, an established negative regulator of IFNgamma signaling, is highly up-regulated during infection and suppresses STAT1 phosphorylation. Functional analyses revealed that this interference with IFNgamma signaling is accompanied by the suppression of IP-10 production and iNOS induction resulting in increased intracellular bacterial survival. Importantly, the suppressive effect on IFNgamma-mediated host cell protection is most effective when IFNgamma is added post infection, suggesting that the bacteria establish a permissive environment within the host cell.
    MeSH term(s) Animals ; Cell Line ; Cell Proliferation/drug effects ; Francisella tularensis/cytology ; Francisella tularensis/drug effects ; Humans ; Interferon-gamma/immunology ; Interferon-gamma/pharmacology ; Leukocytes, Mononuclear/drug effects ; Leukocytes, Mononuclear/immunology ; Leukocytes, Mononuclear/microbiology ; Macrophages/drug effects ; Macrophages/enzymology ; Macrophages/microbiology ; Mice ; Microbial Viability/drug effects ; Microbial Viability/immunology ; Models, Immunological ; Monocytes/drug effects ; Monocytes/immunology ; Monocytes/microbiology ; Nitric Oxide/biosynthesis ; Nitric Oxide Synthase Type II/metabolism ; Phagocytes/drug effects ; Phagocytes/immunology ; Phagocytes/microbiology ; Phagosomes/drug effects ; Phagosomes/microbiology ; Phosphorylation/drug effects ; STAT1 Transcription Factor/metabolism ; Suppressor of Cytokine Signaling 3 Protein ; Suppressor of Cytokine Signaling Proteins/metabolism ; Tularemia/immunology ; Tularemia/microbiology
    Chemical Substances STAT1 Transcription Factor ; Socs3 protein, mouse ; Stat1 protein, mouse ; Suppressor of Cytokine Signaling 3 Protein ; Suppressor of Cytokine Signaling Proteins ; Nitric Oxide (31C4KY9ESH) ; Interferon-gamma (82115-62-6) ; Nitric Oxide Synthase Type II (EC 1.14.13.39)
    Language English
    Publishing date 2008-06-02
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 424427-8
    ISSN 1872-9142 ; 0161-5890
    ISSN (online) 1872-9142
    ISSN 0161-5890
    DOI 10.1016/j.molimm.2008.04.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: MiR-155 induction by F. novicida but not the virulent F. tularensis results in SHIP down-regulation and enhanced pro-inflammatory cytokine response.

    Cremer, Thomas J / Ravneberg, David H / Clay, Corey D / Piper-Hunter, Melissa G / Marsh, Clay B / Elton, Terry S / Gunn, John S / Amer, Amal / Kanneganti, Thirumala-Devi / Schlesinger, Larry S / Butchar, Jonathan P / Tridandapani, Susheela

    PloS one

    2009  Volume 4, Issue 12, Page(s) e8508

    Abstract: The intracellular gram-negative bacterium Francisella tularensis causes the disease tularemia and is known for its ability to subvert host immune responses. Previous work from our laboratory identified the PI3K/Akt pathway and SHIP as critical modulators ...

    Abstract The intracellular gram-negative bacterium Francisella tularensis causes the disease tularemia and is known for its ability to subvert host immune responses. Previous work from our laboratory identified the PI3K/Akt pathway and SHIP as critical modulators of host resistance to Francisella. Here, we show that SHIP expression is strongly down-regulated in monocytes and macrophages following infection with F. tularensis novicida (F.n.). To account for this negative regulation we explored the possibility that microRNAs (miRs) that target SHIP may be induced during infection. There is one miR that is predicted to target SHIP, miR-155. We tested for induction and found that F.n. induced miR-155 both in primary monocytes/macrophages and in vivo. Using luciferase reporter assays we confirmed that miR-155 led to down-regulation of SHIP, showing that it specifically targets the SHIP 3'UTR. Further experiments showed that miR-155 and BIC, the gene that encodes miR-155, were induced as early as four hours post-infection in primary human monocytes. This expression was dependent on TLR2/MyD88 and did not require inflammasome activation. Importantly, miR-155 positively regulated pro-inflammatory cytokine release in human monocytes infected with Francisella. In sharp contrast, we found that the highly virulent type A SCHU S4 strain of Francisella tularensis (F.t.) led to a significantly lower miR-155 response than the less virulent F.n. Hence, F.n. induces miR-155 expression and leads to down-regulation of SHIP, resulting in enhanced pro-inflammatory responses. However, impaired miR-155 induction by SCHU S4 may help explain the lack of both SHIP down-regulation and pro-inflammatory response and may account for the virulence of Type A Francisella.
    MeSH term(s) Animals ; Base Sequence ; Caspase 1/metabolism ; Cell Line ; Cytokines/biosynthesis ; Cytokines/immunology ; Down-Regulation/genetics ; Endocytosis ; Enzyme Activation ; Francisella/cytology ; Francisella/physiology ; Francisella tularensis/pathogenicity ; Gram-Negative Bacterial Infections/enzymology ; Gram-Negative Bacterial Infections/genetics ; Humans ; Inflammation Mediators/immunology ; Inflammation Mediators/metabolism ; Inositol Polyphosphate 5-Phosphatases ; Mice ; MicroRNAs/genetics ; MicroRNAs/metabolism ; Microbial Viability ; Models, Biological ; Molecular Sequence Data ; Phosphoric Monoester Hydrolases/genetics ; Phosphoric Monoester Hydrolases/metabolism ; Signal Transduction ; Toll-Like Receptors ; Virulence/genetics
    Chemical Substances Cytokines ; Inflammation Mediators ; MIRN155 microRNA, human ; MicroRNAs ; Mirn155 microRNA, mouse ; Toll-Like Receptors ; Phosphoric Monoester Hydrolases (EC 3.1.3.2) ; Inositol Polyphosphate 5-Phosphatases (EC 3.1.3.56) ; Caspase 1 (EC 3.4.22.36)
    Language English
    Publishing date 2009-12-30
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0008508
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Changes in the three-dimensional angular vestibulo-ocular reflex following intratympanic gentamicin for Ménière's disease.

    Carey, John P / Minor, Lloyd B / Peng, Grace C Y / Della Santina, Charles C / Cremer, Phillip D / Haslwanter, Thomas

    Journal of the Association for Research in Otolaryngology : JARO

    2002  Volume 3, Issue 4, Page(s) 430–443

    Abstract: The 3-dimensional angular vestibulo-ocular reflexes (AVOR) elicited by rapid rotary head thrusts were studied in 17 subjects with unilateral Ménière's disease before and 2-10 weeks after treatment with intratympanic gentamicin and in 13 subjects after ... ...

    Abstract The 3-dimensional angular vestibulo-ocular reflexes (AVOR) elicited by rapid rotary head thrusts were studied in 17 subjects with unilateral Ménière's disease before and 2-10 weeks after treatment with intratympanic gentamicin and in 13 subjects after surgical unilateral vestibular destruction (SUVD). Each head thrust was in the horizontal plane or in either diagonal plane of the vertical semicircular canals, so that each head thrust effectively stimulated only one pair of canals. The AVOR gains (eye velocity/head velocity during the 30 ms before peak head velocity) for the head thrusts exciting each individual canal were averaged and taken as a measure of the function of that canal. Prior to intratympanic gentamicin, gains for head thrusts that excited canals on the affected side were 0.91 +/- 0.20 (horizontal canal, HC), 0.78 +/- 0.20 (anterior canal, AC), and 0.83 +/- 0.10 (posterior canal, PC). The asymmetries between these gain values and those for head thrusts that excited the contralateral canals were <2%. In contrast, caloric asymmetries averaged 40% +/- 32%. Intratympanic gentamicin resulted in decreased gains attributable to each canal on the treated side: 0.40 +/- 0.12 (HC), 0.35 +/- 0.14 (AC), 0.31 +/- 0.14 (PC) (p <0.01). However, the gains attributable to contralateral canals dropped only slightly, resulting in marked asymmetries between gains for excitation of ipsilateral canals versus their contralateral mates: HC: 34% +/- 12%, AC: 24% +/- 25%, and PC: 42% +/- 13%. There was no difference in the AVOR gain for excitation of the ipsilateral HC after gentamicin in patients who received a single intratympanic injection (0.39 +/- 0.11, n = 12) in comparison to those who received 2-3 injections (0.42 +/- 0.15, n = 5, p = 0.7). Gain decreases attributed to the gentamicin-treated HC and AC were not as severe as those observed after SUVD. This finding suggests that intratympanic gentamicin causes a partial vestibular lesion that may involve preservation of spontaneous discharge and/or rotational sensitivity of afferents.
    MeSH term(s) Adult ; Aged ; Cold Temperature ; Female ; Gentamicins/administration & dosage ; Head/physiopathology ; Humans ; Male ; Meniere Disease/complications ; Meniere Disease/drug therapy ; Meniere Disease/physiopathology ; Meniere Disease/surgery ; Middle Aged ; Movement ; Nystagmus, Pathologic/etiology ; Nystagmus, Pathologic/physiopathology ; Reflex, Vestibulo-Ocular/drug effects ; Retreatment ; Semicircular Canals/physiopathology ; Therapeutic Irrigation ; Time Factors ; Tympanic Membrane/physiopathology ; Vertigo/etiology ; Vertigo/physiopathology ; Vestibule, Labyrinth/surgery
    Chemical Substances Gentamicins
    Language English
    Publishing date 2002-12
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 2021417-0
    ISSN 1438-7573 ; 1525-3961
    ISSN (online) 1438-7573
    ISSN 1525-3961
    DOI 10.1007/s101620010053
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Accuracy of Cuff-Measured Blood Pressure: Systematic Reviews and Meta-Analyses.

    Picone, Dean S / Schultz, Martin G / Otahal, Petr / Aakhus, Svend / Al-Jumaily, Ahmed M / Black, J Andrew / Bos, Willem J / Chambers, John B / Chen, Chen-Huan / Cheng, Hao-Min / Cremer, Antoine / Davies, Justin E / Dwyer, Nathan / Gould, Brian A / Hughes, Alun D / Lacy, Peter S / Laugesen, Esben / Liang, Fuyou / Melamed, Roman /
    Muecke, Sandy / Ohte, Nobuyuki / Okada, Sho / Omboni, Stefano / Ott, Christian / Peng, Xiaoqing / Pereira, Telmo / Pucci, Giacomo / Rajani, Ronak / Roberts-Thomson, Philip / Rossen, Niklas B / Sueta, Daisuke / Sinha, Manish D / Schmieder, Roland E / Smulyan, Harold / Srikanth, Velandai K / Stewart, Ralph / Stouffer, George A / Takazawa, Kenji / Wang, Jiguang / Westerhof, Berend E / Weber, Franz / Weber, Thomas / Williams, Bryan / Yamada, Hirotsugu / Yamamoto, Eiichiro / Sharman, James E

    Journal of the American College of Cardiology

    2017  Volume 70, Issue 5, Page(s) 572–586

    Abstract: Background: Hypertension (HTN) is the single greatest cardiovascular risk factor worldwide. HTN management is usually guided by brachial cuff blood pressure (BP), but questions have been raised regarding accuracy.: Objectives: This comprehensive ... ...

    Abstract Background: Hypertension (HTN) is the single greatest cardiovascular risk factor worldwide. HTN management is usually guided by brachial cuff blood pressure (BP), but questions have been raised regarding accuracy.
    Objectives: This comprehensive analysis determined the accuracy of cuff BP and the consequent effect on BP classification compared with intra-arterial BP reference standards.
    Methods: Three individual participant data meta-analyses were conducted among studies (from the 1950s to 2016) that measured intra-arterial aortic BP, intra-arterial brachial BP, and cuff BP.
    Results: A total of 74 studies with 3,073 participants were included. Intra-arterial brachial systolic blood pressure (SBP) was higher than aortic values (8.0 mm Hg; 95% confidence interval [CI]: 5.9 to 10.1 mm Hg; p < 0.0001) and intra-arterial brachial diastolic BP was lower than aortic values (-1.0 mm Hg; 95% CI: -2.0 to -0.1 mm Hg; p = 0.038). Cuff BP underestimated intra-arterial brachial SBP (-5.7 mm Hg; 95% CI: -8.0 to -3.5 mm Hg; p < 0.0001) but overestimated intra-arterial diastolic BP (5.5 mm Hg; 95% CI: 3.5 to 7.5 mm Hg; p < 0.0001). Cuff and intra-arterial aortic SBP showed a small mean difference (0.3 mm Hg; 95% CI: -1.5 to 2.1 mm Hg; p = 0.77) but poor agreement (mean absolute difference 8.0 mm Hg; 95% CI: 7.1 to 8.9 mm Hg). Concordance between BP classification using the Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure cuff BP (normal, pre-HTN, and HTN stages 1 and 2) compared with intra-arterial brachial BP was 60%, 50%, 53%, and 80%, and using intra-arterial aortic BP was 79%, 57%, 52%, and 76%, respectively. Using revised intra-arterial thresholds based on cuff BP percentile rank, concordance between BP classification using cuff BP compared with intra-arterial brachial BP was 71%, 66%, 52%, and 76%, and using intra-arterial aortic BP was 74%, 61%, 56%, and 65%, respectively.
    Conclusions: Cuff BP has variable accuracy for measuring either brachial or aortic intra-arterial BP, and this adversely influences correct BP classification. These findings indicate that stronger accuracy standards for BP devices may improve cardiovascular risk management.
    MeSH term(s) Blood Pressure/physiology ; Blood Pressure Determination/instrumentation ; Cardiovascular Diseases/diagnosis ; Cardiovascular Diseases/physiopathology ; Equipment Design ; Reproducibility of Results
    Language English
    Publishing date 2017-07-27
    Publishing country United States
    Document type Journal Article ; Meta-Analysis ; Review
    ZDB-ID 605507-2
    ISSN 1558-3597 ; 0735-1097
    ISSN (online) 1558-3597
    ISSN 0735-1097
    DOI 10.1016/j.jacc.2017.05.064
    Database MEDical Literature Analysis and Retrieval System OnLINE

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