Sökning: WFRF:(Wahlund Lars O.) > (2005-2009) > Progression of whit...
Fältnamn | Indikatorer | Metadata |
---|---|---|
000 | 05347naa a2201033 4500 | |
001 | oai:gup.ub.gu.se/98800 | |
003 | SwePub | |
008 | 240528s2008 | |||||||||||000 ||eng| | |
009 | oai:prod.swepub.kib.ki.se:116999472 | |
024 | 7 | a https://gup.ub.gu.se/publication/988002 URI |
024 | 7 | a https://doi.org/10.1161/STROKEAHA.107.4985352 DOI |
024 | 7 | a http://kipublications.ki.se/Default.aspx?queryparsed=id:1169994722 URI |
040 | a (SwePub)gud (SwePub)ki | |
041 | a eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Gouw, Alida A4 aut |
245 | 1 0 | a Progression of white matter hyperintensities and incidence of new lacunes over a 3-year period: the Leukoaraiosis and Disability study. |
264 | 1 | c 2008 |
520 | a BACKGROUND AND PURPOSE: We studied the natural course of white matter hyperintensities (WMH) and lacunes, the main MRI representatives of small vessel disease, over time and evaluated possible predictors for their development. METHODS: Baseline and repeat MRI (3-year follow-up) were collected within the multicenter, multinational Leukoaraiosis and Disability study (n=396). Baseline WMH were scored on MRI by the Fazekas scale and the Scheltens scale. WMH progression was assessed using the modified Rotterdam Progression scale (absence/presence of progression in 9 brain regions). Baseline and new lacunes were counted per region. WMH and lacunes at baseline and vascular risk factors were evaluated as predictors of WMH progression and new lacunes. RESULTS: WMH progressed (mean+/-SD=1.9+/-1.8) mostly in the subcortical white matter, where WMH was also most prevalent at baseline. The majority of new lacunes, which were found in 19% of the subjects (maximum=9), also appeared in the subcortical white matter, mainly of the frontal lobes, whereas most baseline lacunes were located in the basal ganglia. Baseline WMH and lacunes predicted both WMH progression and new lacunes. Furthermore, previous stroke, diabetes, and blood glucose were risk factors for WMH progression. Male sex, hypertension, systolic blood pressure, previous stroke, body mass index, high-density lipoprotein, and triglyceride levels were risk factors for new lacunes. CONCLUSIONS: WMH and lacunes progressed over time, predominantly in the subcortical white matter. Progression was observed especially in subjects with considerable WMH and lacunes at baseline. Moreover, the presence of vascular risk factors at baseline predicted WMH progression and new lacunes over a 3-year period. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Psykiatri0 (SwePub)302152 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Psychiatry0 (SwePub)302152 hsv//eng |
653 | a Aged | |
653 | a Aged | |
653 | a 80 and over | |
653 | a Basal Ganglia | |
653 | a blood supply | |
653 | a pathology | |
653 | a physiopathology | |
653 | a Brain | |
653 | a blood supply | |
653 | a pathology | |
653 | a physiopathology | |
653 | a Brain Infarction | |
653 | a epidemiology | |
653 | a pathology | |
653 | a physiopathology | |
653 | a Brain Ischemia | |
653 | a epidemiology | |
653 | a pathology | |
653 | a physiopathology | |
653 | a Cardiovascular Diseases | |
653 | a epidemiology | |
653 | a Cerebral Arteries | |
653 | a pathology | |
653 | a physiopathology | |
653 | a Comorbidity | |
653 | a Disease Progression | |
653 | a Female | |
653 | a Follow-Up Studies | |
653 | a Frontal Lobe | |
653 | a blood supply | |
653 | a pathology | |
653 | a physiopathology | |
653 | a Humans | |
653 | a Hyperlipidemias | |
653 | a epidemiology | |
653 | a Incidence | |
653 | a Leukoaraiosis | |
653 | a epidemiology | |
653 | a pathology | |
653 | a physiopathology | |
653 | a Magnetic Resonance Imaging | |
653 | a Male | |
653 | a Nerve Fibers | |
653 | a Myelinated | |
653 | a pathology | |
653 | a Prevalence | |
653 | a Risk Factors | |
653 | a Time Factors | |
700 | 1 | a van der Flier, Wiesje M4 aut |
700 | 1 | a Fazekas, Franz4 aut |
700 | 1 | a van Straaten, Elisabeth C W4 aut |
700 | 1 | a Pantoni, Leonardo4 aut |
700 | 1 | a Poggesi, Anna4 aut |
700 | 1 | a Inzitari, Domenico4 aut |
700 | 1 | a Erkinjuntti, Timo4 aut |
700 | 1 | a Wahlund, Lars Ou Karolinska Institutet4 aut |
700 | 1 | a Waldemar, Gunhild4 aut |
700 | 1 | a Schmidt, Reinhold4 aut |
700 | 1 | a Scheltens, Philip4 aut |
700 | 1 | a Barkhof, Frederik4 aut |
700 | 1 | a Wallin, Anders,d 1950u Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry4 aut0 (Swepub:gu)xwaand |
710 | 2 | a Karolinska Institutetb Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi4 org |
773 | 0 | t Stroke; a journal of cerebral circulationg 39:5, s. 1414-20q 39:5<1414-20x 1524-4628 |
856 | 4 8 | u https://gup.ub.gu.se/publication/98800 |
856 | 4 8 | u https://doi.org/10.1161/STROKEAHA.107.498535 |
856 | 4 8 | u http://kipublications.ki.se/Default.aspx?queryparsed=id:116999472 |
Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.