Læknablaðið : fylgirit - 01.08.2003, Blaðsíða 20

Læknablaðið : fylgirit - 01.08.2003, Blaðsíða 20
■ ABSTRACTS / 27TH NORDIC PSYCHIATRIC CONGRESS Objective: Severe cognitive impairment is common in elderly patients with schizophrenia. Alzheimer’s disease (AD) is the main cause of dementia among the elderly. Biochemical and genetic studies suggest that amyloid beta-peptide (Ab) is central in AD. We examined the possible involvement of Ab in cognitive impairment in schizophrenia. Method: Specific antibodies against two major forms of Ab, Ab40 and Ab42, were used in ELISA assays to determine the levels of Ab in postmortem brains from AD patients (N=10), controls (N=ll), and schizophrenia patients with (N=7) or without (N=26) AD. Kesults: The levels of amyloid b-peptide were highest in the AD, followed by the patients with schizophrenia and controls. The mean Ab42 level in the schizophrenia patients without AD was similar to that in the controls, but the level in the schizophrenia patients with AD was significantly higher than in those without AD or controls. The Ab42 level in the schizophrenia patients with AD was significantly lower than the level in the AD. Conclusions: In contrast to elderly schizophrenia patients with AD pathology, those without AD had Ab levels that were not signifi- cantly different from those of normal subjects; hence Ab does not account for the cognitive deficits in this group. Tliese results suggest that the causes of cognitive impairment in “pure” schizophrenia are different from those in AD. The decrease of Ab in schizophrenia patients with AD as compared to patients only with AD may be due to the neuroleptic treatment or the heavy smoking, as haloperi- dol and nicotine decrease the Ab levels. F-6/3 Friday 15/8,15:00-16:00 Simvastatin treatment lowers both alpha- and beta- cleaved app in Alzheimer’s disease Magnus Sjögren, Associate Professor, Institute of Clinical Neuroscience, SE413 45 Goteborg, Sweden. K Gustafsson, S Syversen, A Olsson, A Wallin, K Blennow. magnus.sjogren@medfak.gu.se We investigated the clinical and biological effects of cholesterol- lowering treatment with a statin in 19 patients with Alzheimer’s disease. All patients received simvastatin 20 mg/day for 12 weeks in an open trial. Primary efficacy parameters were the changes after 12 weeks in the cerebrospinal fluid (CSF) levels of beta-amyIoid42 (AB42), alpha-secretase-cleaved APP (alpha-sAPP), beta-secre- tase-cleaved APP (beta-sAPP), tau, phospho-tau and the plasma levels of beta-amyloid (AB). A secondary efficacy parameter was the change in ADAS-cog score. After 12 weeks, CSF alpha-sAPP and CSF beta-sAPP were significantly reduced (p<0.001), but the CSF levels of tau, phospho-tau, AB42 and the plasma levels of AB were unchanged. The ADAS-cog score was slightly increased (p<0.05). Furthermore, a decrease in total-cholesterol levels was found at 12 weeks although all patients had normal levels at base- line. The results suggest that simvastatin acts directly on the proces- sing of APP by inhibiting both the alpha- and the beta-secretase pathways. Results of 12-month follow-up and comparison with the effects of statin treatment in vascular dementia will also be pre- sented. F-6/4 Friday 15/8,15:00-16:00 Co-occurrence of anxiety, depression and alcholism Halldór Kolbeinssun, MD, Psychiatrist, Landspítali University Hospital, Reykjavík, Dept. Psychiatry at Kleppur, Iceland. H Óskarsson, JG Stefánsson, Þ Þorgeirsson, K Stefánsson. halldork@landspitali. is Aims: To investigate the co-occurrence of depressive disorders and alcoholism among subjects diagnosed with anxiety disorders. Method: The study is based on the screening for anxiety and de- pression in a population sample, followed by diagnostic work-up with the computerized version of the Composite International Diagnostic Interview (CIDI). ICs have to meet criteria for either an ICD-10 or a DSM 3-R anxiety diagnosis. Results: 1.136 cases were diagnosed with a lifetime diagnosis of anxiety disorders. Thereof 67% had a depressive disorder. Co-morbid alcoholism was found in 31.8% of those with anxiety; 19.8% of the females and in 48,5% of the males. The presence of depression with anxiety would increase the number of those with alcoholism. The mean Age of Onset (AGO) of alcoholism in this group is 24.8 years; the AGO of all the anxiety disorders, except Generalized Anxiety Disorder, have an earlier onset. AGO of depression is 25.3 years. Conclusion: The prevalence of alcoholism is high in our cohort of individuals with anxiety disorders, much higher than expected when compared with prevalence studies of alcoholism in the Icelandic population. The co-morbidity of alcoholism was still higher when there was co-occurrence of depression and anxiety disorders. It is noteworthy from an etiological point of view that alcoholism rarely precedes the onset of most affective disorders. F - 7 / 1 Friday 15/8,15:00-16:00 Patterns of antipsychotic use and side-effects in a lst episode psychosis service Páll Multhíusson, Dr., Section of Early Psychosis, Institute Of Psychiatry, Institute Of Psychiatry, PO BOX 67, DeCresigny Park, London SE4 1AR, UK. P Power, P McGuire. p. matthiasson @iop. kcl. ac. uk Background: Lambeth, an inner city area in South London has a very high incidence of psychosis. Patients are managed by The Lambeth Early Onset (LEO) service, a specialised community team, those with severe symptoms are admitted to a 18-bed inpatient unit. Aims: This audit looked at patterns of antipsychotic use in the LEO service. Methods: We reviewed patterns to care, diagnoses, antipsychotic medication and side-effects in patients with lst episode of psychosis presenting over a 12-month period. This was a retrospective case note review over the first 3-6 months of each individual’s treatment. Results: Fifty-two patients (28 males, 24 females) were enrolled, just over half of admissions. The majority presented with non- affective psychosis. The most commonly used antipsychotics were risperidone, olanzapine and quetiapine. The doses prescribed were low and there was a good clinical response in the majority of cases. Side-effects occurred in 39% of patients. In 13.5% they led to with- drawal of medication. One patient had repeated urinary retention, one developed diabetes mellitus. 20 LÆKNABLADIÐ / FYLGIRIT 48 2003/89
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