Læknablaðið : fylgirit - 01.05.2002, Blaðsíða 39

Læknablaðið : fylgirit - 01.05.2002, Blaðsíða 39
POSTERS / 3 3RD SNC & 2ND SCNN POSTERS P01 - Hyperhomocysteinemia. A Risk Factor of Stroke and Recurrent Stroke Brander T, Christensen H, Gideon R, Truelsen T, Boysen G Department of Neurology and Department of Clinical Biochemistry, Bispebjerg Hospital, Denmark Objective: The levels of s-homocystein (s-hcy) were compared in patients with transient ischemic attachs (TIA), ischemic stroke and hemorrhagic stroke. We evaluated s-hcy measured the day after admission as a predictor of recurrent stroke within the following year. Methods: 944 patients were admitted at the Department of Neuro- logy, Bispebjerg Hospital with the diagnoses TIA (n=190), ischemic stroke (n=634) or hemorrhagic stroke (n=120). The patients' mean levels of s-hcy were compared in the three diagnoses, and in patients with recurrent stroke versus patients without recurrent stroke during the following year. Due to log normal distribution, data was analysed after log 10 transformation. A multivariate logis- tic regression model was set up after univariate analysis including variables at a significance level of 0.1. Results: Patients with an ischemic event (TIA or ischemic stroke) (n=824) had a mean s-hcy of 11.99 (j.mol/1 (CI 95%: 11.64-12.39), patients with hemorrhagic stroke had a mean s-hcy of 10.52 p.mol/1 (CI 95%: 9.73-11.38). The difference between the two groups was significant, p=0.003. After one year we could document recurrent stroke in 44 cases, these patients had mean s-hcy levels at the primary admission of 14.29 p.mol/1 (CI 95%: 11.51-17.70) whereas patients without recurrent stroke had mean levels of s-hcy of 11.69 p.mol/1 (CI 95%: 11.53-12.27), p=0.005. S-hcy reached significance in multivariate logistic regression model. S-hcy+iofmoi/i OR: 1,4(0 95% 1.2-1.7) p=0.0028 Conclusion: Elevated s-hcy was independently associated with recurrent stroke within the first year after a cerebrovascular event. Our findings corroborate those of other investigators indicating that hyperhomocysteinemia was a risk factor for ischemic stroke. On- going intervention studies will clarify whether treating hyperhomo- cysteinemia can reduce the risk of stroke and recurrent stroke. P02 - Correlation between early TNF-A levels and ischaemic stroke severity Zaremba J1, Losy Ju 'Department of Clinical Neuroimmunology.University School of Medicine, Poznan, Poland, TSeuroimmunological Unit.Institute of Experimental and Clinical Medicine Polish Academy of Sciences, Poznan, Poland Objectives: The study aimed to evaluate the levels of an important proinflammatory cytokine tumour necrosis factor-a (TNF-ot) in cerebrospinal fluid and serum in acute stroke and to study the relation between those and the neurological stroke severity and functional disability. Material and methods: The investigations comprised 23 ischaemic stroke patients. CSF and blood samples were obtained 24h after the onset of stroke, and stored until analysis. Patients were examined according to Scandinavian Stroke Scale (SSS) and to Barthel Index (BI). Results: The patients displayed statistically significant high levels of TNF-a in CSF and sera within the first 24h of stroke. These correlated significantly with SSS and BI scores calculated within the same interval, and 1 and 2 weeks later. Conclusion: The results suggest involvement of TNF-a in mecha- nisms of early stroke-induced inflammation and a predictive value of the initial TNF-a levels for the outcome of stroke. P03 - Entacapone is of benefit in patients with early Parkinson's disease without motor fluctuations Brooks D, Gordin A, Poewe W, Deuschl G, Leinonen M, Kultalahti E-R, Reinikainen K Research Centre, Orion Pharma, Espoo, Finland Objective: It has been shown that entacapone is effective and safe in advanced Parkinson's disease (PD). Entacapone has not earlier been studied in non-lluctuating patients. These patients can still be bradykinetic, and also have other symptoms of PD, irrespective of gaining relief with small doses of dopaminergic drugs. The aim was to study whether patients with PD without motor fluctuations could benefit from combining entacapone with their current levodopa treatment. Material and methods: A multicenter, placebo controlled, double- blind, randomised (2:1 entacapone vs. placebo) six months study was carried out in 29 clinics in the UK and republic of Ireland. The study included 300 PD patients, of whom 128 were classified as non- fluctuating. Entacapone, 200 mg (or placebo) was administered with each daily levodopa dose. Results: The ADL score improved from 10.6 to 10.0 in the entaca- pone compared with a reduction of 0.1 in the placebo group (p<0.01). The scheduled levodopa dose remained practically un- changed in the entacapone group, and increased by 47 mg in the placebo group, the difference being stalistically significant (p<0.01). The effect of entacapone was lost upon withdrawal. The ADL score worsened from the last visit value of 9.9 to a post-study value of 10.6. Conclusion: Adjunct entacapone significantly improved the ADL score in patients without fluctuations. This demonstrates the beneficial effect of the use of entacapone before motor complica- tions are emerging. P04 - Changes in heart rate variability after stroke Kristjánsson B, Hjaltason H, Stefánsson SB Dept. of Neurology, Landspitali University Hospital, Reykjavík, Iceland. Introduction: Heart rate variability (HRV) reflects sympathetic and parasympathetic modulation of the cardiac sinus node. The aim of the present study was to assess disruption of sympathetic/para- sympathetic balance to the heart following stroke using HRV as a probe. Material and methods: Twelve stroke patients admitted to Land- spítali, University Hospital participated in the investigations. These were compared with a control group having similar age and sex distribution and without a history of neurological or cardiac disease. The patients were assessed by means of the National Insti- tute of Health Stroke Scale. The electrocardiogram (ECG) was recorded digitally for ten minutes from all participants. The R Læknablaðið/Fylgirit 43 2002/88 39
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