dc.description.abstract | Introduction/Objective Theaimof thisfollow-upstudywasto determinetheeffectsoftopiramate
therapyoncognitive functionsinpatients withpharmacoresistant focalepilepsy.
MethodsThestudysamplecomprised of40topiramate naivepatients. Thetopiramate startingdose
was25mg,withafortnightly titrationschedule of 25mg.A widerangeofcognitive functions was
evaluated tlllph extensive neuropsychological testingatbaseline andsixmonthsafterreaching the
target dose(200mg/day).
ResultsThemost-common sideeffectsfollowingtheintroductionoftopiramatewerecognitiveimpairments, reportedby45Voofthe participants.The neuropsycholcgical scoreson attention, executive
function, verbal content recall, improvedcognitive flexibiliiy, aswellasvisuospatial abilityandspeech,
obtained atsix-month follow-up weresignificantly lowerthan atbaseline. However, statistically significant
correlation betweenneuropsychologicil scores andthenumber ofantiepileptic Orrqrt.["] ,6rgiid"
topiramate couldnotbeestablished. Similarly, nostatistically significant differences werenotedbetween
thepercentage ofreducedneuropsychological scores atfollow-uppertainingto patientswithlower
andhigherbaseline cognitiveperformance. Moreover, regression analysis indicates thatthepercentagechangeinthemajorityof cognitivescoresisunrelated to theageattheepilepsy onset, epilepsy
duration, presence of brainpathology onmagnetic resonance imagingandpercentage changeinthe
depression scalescore.
Conclusion Despite slowintroduction andadministration ofarelatively small dose, topiramate exhibits
adverse effectsonawiderangeofcognitive functions, whichappear unrelated to thenumber ofadditionalantiepileptic drugs, baseline cognitive functioning, ageattheonsetofepilepsy anditsduration,
presence ofbrainpathology andtheextentofdepressive symptom | en_US |