scholarly journals Effect of Delayed Clozapine Initiation on Acute Treatment Response in Treatment-Resistant Schizophrenia

2021 ◽  
Vol 24 (2) ◽  
pp. 52-59
Author(s):  
So Yung Yang ◽  
Jung-Kyu Choi ◽  
Sunyoung Park ◽  
Jaesub Park
2021 ◽  
Author(s):  
Mu-Hong Chen ◽  
Wei-Chen Lin ◽  
Cheng-Ta Li ◽  
Shih-Jen Tsai ◽  
Hui-Ju Wu ◽  
...  

Abstract Introduction Pretreatment neurocognitive function may predict the treatment response to low-dose ketamine infusion in patients with treatment-resistant depression (TRD). However, the association between working memory function at baseline and the antidepressant efficacy of ketamine infusion remains unclear. Methods A total of 71 patients with TRD were randomized to one of three treatment groups: 0.5 mg/kg ketamine, 0.2 mg/kg ketamine, or normal saline. Depressive symptoms were measured using the 17-item Hamilton Depression Rating Scale (HDRS) at baseline and after treatment. Cognitive function was evaluated using working memory and go-no-go tasks at baseline. Results A generalized linear model with adjustments for demographic characteristics, treatment groups, and total HDRS scores at baseline revealed only a significant effect of working memory function (correct responses and omissions) on the changes in depressive symptoms measured by HDRS at baseline (F=12.862, p<0.05). Correlation analysis further showed a negative relationship (r=0.519, p=0.027) between pretreatment working memory function and changes in HDRS scores in the 0.5 mg/kg ketamine group. Discussion An inverse relationship between pretreatment working memory function and treatment response to ketamine infusion may confirm that low-dose ketamine infusion is beneficial and should be reserved for patients with TRD.


2017 ◽  
Vol 174 (3) ◽  
pp. 216-229 ◽  
Author(s):  
Oliver D. Howes ◽  
Rob McCutcheon ◽  
Ofer Agid ◽  
Andrea de Bartolomeis ◽  
Nico J.M. van Beveren ◽  
...  

2019 ◽  
Vol 5 (6) ◽  
pp. e364 ◽  
Author(s):  
Lisette J.A. Kogelman ◽  
Ann-Louise Esserlind ◽  
Anne Francke Christensen ◽  
Swapnil Awasthi ◽  
Stephan Ripke ◽  
...  

ObjectiveTo assess whether the polygenic risk score (PRS) for migraine is associated with acute and/or prophylactic migraine treatment response.MethodsWe interviewed 2,219 unrelated patients at the Danish Headache Center using a semistructured interview to diagnose migraine and assess acute and prophylactic drug response. All patients were genotyped. A PRS was calculated with the linkage disequilibrium pred algorithm using summary statistics from the most recent migraine genome-wide association study comprising ∼375,000 cases and controls. The PRS was scaled to a unit corresponding to a twofold increase in migraine risk, using 929 unrelated Danish controls as reference. The association of the PRS with treatment response was assessed by logistic regression, and the predictive power of the model by area under the curve using a case-control design with treatment response as outcome.ResultsA twofold increase in migraine risk associates with positive response to migraine-specific acute treatment (odds ratio [OR] = 1.25 [95% confidence interval (CI) = 1.05–1.49]). The association between migraine risk and migraine-specific acute treatment was replicated in an independent cohort consisting of 5,616 triptan users with prescription history (OR = 3.20 [95% CI = 1.26–8.14]). No association was found for acute treatment with non–migraine-specific weak analgesics and prophylactic treatment response.ConclusionsThe migraine PRS can significantly identify subgroups of patients with a higher-than-average likelihood of a positive response to triptans, which provides a first step toward genetics-based precision medicine in migraine.


2015 ◽  
Vol 35 (9) ◽  
pp. 1603-1605 ◽  
Author(s):  
Savvas Psarelis ◽  
Doros Polydorou ◽  
Sophia Corsava ◽  
Constantinos Aristotelous

2004 ◽  
Vol 38 (2) ◽  
pp. 163-168 ◽  
Author(s):  
Alp Üçok ◽  
Aslιhan Polat ◽  
Aysun Genç ◽  
Sibel Çakιr ◽  
Nurten Turan

2011 ◽  
Vol 21 ◽  
pp. S472-S473
Author(s):  
M. Buoli ◽  
M. Serati ◽  
A. Caldiroli ◽  
A.C. Altamura

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