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Sökning: WFRF:(Niemelä O.)

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1.
  • Globisch, Maria A., et al. (författare)
  • Immunothrombosis and vascular heterogeneity in cerebral cavernous malformation
  • 2022
  • Ingår i: Blood. - : American Society of Hematology. - 0006-4971 .- 1528-0020. ; 140:20, s. 2154-2169
  • Tidskriftsartikel (refereegranskat)abstract
    • Cerebral cavernous malformation (CCM) is a neurovascular disease that results in various neurological symptoms. Thrombi have been reported in surgically resected CCM patient biopsies, but the molecular signatures of these thrombi remain elusive. Here, we investigated the kinetics of thrombi formation in CCM and how thrombi affect the vasculature and contribute to cerebral hypoxia. We used RNA sequencing to investigate the transcriptome of mouse brain endothelial cells with an inducible endothelial-specific Ccm3 knock-out (Ccm3-iECKO). We found that Ccm3-deficient brain endothelial cells had a higher expression of genes related to the coagulation cascade and hypoxia when compared with wild-type brain endothelial cells. Immunofluorescent assays identified key molecular signatures of thrombi such as fibrin, von Willebrand factor, and activated platelets in Ccm3-iECKO mice and human CCM biopsies. Notably, we identified polyhedrocytes in Ccm3-iECKO mice and human CCM biopsies and report it for the first time. We also found that the parenchyma surrounding CCM lesions is hypoxic and that more thrombi correlate with higher levels of hypoxia. We created an in vitro model to study CCM pathology and found that human brain endothelial cells deficient for CCM3 expressed elevated levels of plasminogen activator inhibitor-1 and had a redistribution of von Willebrand factor. With transcriptomics, comprehensive imaging, and an in vitro CCM preclinical model, this study provides experimental evidence that genes and proteins related to the coagulation cascade affect the brain vasculature and promote neurological side effects such as hypoxia in CCMs. This study supports the concept that antithrombotic therapy may be beneficial for patients with CCM.
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2.
  • Ilmarinen, P., et al. (författare)
  • Long-term adherence to inhaled corticosteroids in clinical phenotypes of adult-onset asthma
  • 2021
  • Ingår i: Journal of Allergy and Clinical Immunology: In Practice. - : Elsevier BV. - 2213-2198. ; 9:9
  • Tidskriftsartikel (refereegranskat)abstract
    • Long-term adherence to inhaled corticosteroids was 75% or greater in phenotypes with the poorest outcome but did not differ significantly among clusters. Poor outcome in the most severe phenotypes was not related to poor adherence to inhaled corticosteroid medication.
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3.
  • Niemelä, Matti, et al. (författare)
  • Randomized Comparison of Final Kissing Balloon Dilatation Versus No Final Kissing Balloon Dilatation in Patients With Coronary Bifurcation Lesions Treated With Main Vessel Stenting : The nordic-baltic bifurcation study III
  • 2011
  • Ingår i: Circulation. - 0009-7322 .- 1524-4539. ; 123:1, s. 79-86
  • Tidskriftsartikel (refereegranskat)abstract
    • Background-It is unknown whether the preferred 1-stent bifurcation stenting approach with stenting of the main vessel (MV) and optional side branch stenting using drug-eluting stents should be finalized by a kissing balloon dilatation (FKBD). Therefore, we compared strategies of MV stenting with and without FKBD. Methods and Results-We randomized 477 patients with a bifurcation lesion to FKBD (n=238) or no FKBD (n=239) after MV stenting. The primary end point was major adverse cardiac events: cardiac death, non-procedure-related index lesion myocardial infarction, target lesion revascularization, or stent thrombosis within 6 months. The 6-month major adverse cardiac event rates were 2.1% and 2.5% (P=1.00) in the FKBD and no-FKBD groups, respectively. Procedure and fluoroscopy times were longer and more contrast media was needed in the FKBD group than in the no-FKBD group. Three hundred twenty-six patients had a quantitative coronary assessment. At 8 months, the rate of binary (re) stenosis in the entire bifurcation lesion (MV and side branch) was 11.0% versus 17.3% (P=0.11), in the MV was 3.1% versus 2.5% (P=0.68), and in the side branch was 7.9% versus 15.4% (P=0.039) in the FKBD versus no-FKBD groups, respectively. In patients with true bifurcation lesions, the side branch restenosis rate was 7.6% versus 20.0% (P=0.024) in the FKBD and no-FKBD groups, respectively. Conclusions-MV stenting strategies with and without FKBD were associated with similar clinical outcomes. FKBD reduced angiographic side branch (re) stenosis, especially in patients with true bifurcation lesions. The simple no-FKBD procedures resulted in reduced use of contrast media and shorter procedure and fluoroscopy times. Long-term data on stent thrombosis are needed. Clinical Trial Registration-URL: http://clinicaltrials.gov. Unique identifier: NCT00914199. (Circulation. 2011;123:79-86.)
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4.
  • Skrifvars, Mikael, et al. (författare)
  • Process cure monitoring of unsaturated polyester resins, vinyl ester resins, and gel coats by Raman spectroscopy
  • 2004
  • Ingår i: Journal of Applied Polymer Science. - : Wiley. - 0021-8995 .- 1097-4628. ; 93:3, s. 1285-1292
  • Tidskriftsartikel (refereegranskat)abstract
    • The curing process of unsaturated polyester resins, vinyl ester resins, and gel coats was studied by using a process Raman spectrometer, equipped with a remote fiber-optic probe. The resins were cured and Raman spectra were recorded during the curing reaction. The spectral changes were identified and, from the intensities, the cure process could be monitored. Gel times given by the resin suppliers correlated well with the Raman results. It could also be seen that the curing process continues for a long time, up to several weeks. Postcuring will finally complete the curing process, White and lightly colored gel coats could easily be monitored by Raman spectroscopy, but fluorescent problems were encountered with heavily colored pigments. The curing of laminates containing 50-70 wt % glass fiber mat could also be followed by Raman spectroscopy. © 2004 Wiley Periodicals, Inc.
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