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            "title": "Efficacy of antidepressive medication for depression in Parkinson disease: a network meta-analysis",
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                    "firstName": "Chuanjun",
                    "lastName": "Zhuo"
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            "abstractNote": "BACKGROUND: Parkinson disease (PD) was considered as the 2nd most prevalent neurodegenerative disorder after Alzheimer disease, while depression is a prevailing nonmotor symptom of PD. Typically used antidepression medication includes tricyclic antidepressants (TCA), selective serotonin reuptake inhibitors (SSRI), serotonin and norepinephrine reuptake inhibitors (SNRI), monoamine-oxidase inhibitors (MAOI), and dopamine agonists (DA). Our study aimed at evaluating the efficacy of antidepressive medications for depression of PD.\nMETHODS: Web of Science, PubMed, Embase, and the Cochrane library were searched for related articles. Traditional meta-analysis and network meta-analysis (NMA) were performed with outcomes including depression score, UPDRS-II, UPDRS-III, and adverse effects. Surface under the cumulative ranking curve (SUCRA) was also performed to illustrate the rank probabilities of different medications on various outcomes. The consistency of direct and indirect evidence was also assessed by node-splitting method.\nRESULTS: Results of traditional pairwise meta-analysis were performed. Concerning depression score, significant improvement was observed in AD, MAOI, SSRI, and SNRI compared with placebo. NMA was performed and more information could be obtained. DA was illustrated to be effective over placebo concerning UPDRS-III, MAOI, and SNRI. DA demonstrated a better prognosis in UPDRS-II scores compared with placebo and MAOI. However, DA and SSRI demonstrated a significant increase in adverse effects compared with placebo. The SUCRA value was calculated to evaluate the ranking probabilities of all medications on investigated outcomes, and the consistency between direct and indirect evidences was assessed by node-splitting method.\nCONCLUSION: SSRI had a satisfying efficacy for the depression of PD patients and could improve activities of daily living and motor function of patient but the adverse effects are unneglectable. SNRI are the safest medication with high efficacy for depression as well while other outcomes are relatively poor.",
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            "title": "Sertraline for the treatment of depression in Alzheimer’s disease",
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                    "creatorType": "author",
                    "firstName": "Paul B.",
                    "lastName": "Rosenberg"
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                {
                    "creatorType": "author",
                    "firstName": "Lea T.",
                    "lastName": "Drye"
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                {
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                    "firstName": "Barbara K.",
                    "lastName": "Martin"
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                    "creatorType": "author",
                    "firstName": "Constantine",
                    "lastName": "Frangakis"
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                {
                    "creatorType": "author",
                    "firstName": "Jacobo E.",
                    "lastName": "Mintzer"
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                {
                    "creatorType": "author",
                    "firstName": "Daniel",
                    "lastName": "Weintraub"
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                {
                    "creatorType": "author",
                    "firstName": "Anton P.",
                    "lastName": "Porsteinsson"
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                {
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                    "firstName": "Lon S.",
                    "lastName": "Schneider"
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                {
                    "creatorType": "author",
                    "firstName": "Peter V.",
                    "lastName": "Rabins"
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                    "firstName": "Curtis L.",
                    "lastName": "Meinert"
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                    "firstName": "Constantine G.",
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            "abstractNote": "Background\nDepression is common in Alzheimer’s disease [AD], and antidepressants are commonly used for its treatment, yet evidence for antidepressant efficacy in this population is lacking. We conducted a multi-center, randomized, placebo-controlled trial titled “Depression in Alzheimer’s Disease-2” (DIADS-2) to assess the efficacy and tolerability of sertraline for depression in AD.\n\nMethods\nOne hundred thiry-one participants from 5 U.S. medical centers with mild-to-moderate AD (Mini-Mental State Examination [MMSE] scores 10–26) and depression of AD were randomized to double-blinded treatment with sertraline (N=67) or placebo (N=64), with a target dosage of 100 mg daily. Efficacy was assessed using logistic regressions and mixed effects models in an intention to treat (ITT) analysis with imputation of missing data. Principal outcome measures were modified Alzheimer’s Disease Cooperative Study-Clinical Global Impression of Change (mADCS-CGIC), change in Cornell Scale for Depression in Dementia (CSDD) scores, and remission defined by both mADCS-CGIC score ≤2 and CSDD score ≤ 6.\n\nFindings\nmADCS-CGIC ratings (OR = 1.01 (95% CI: 0.52, 1.97, p=0.98), CSDD scores (median difference at 12 weeks 1.2,[95% CI -1.65, 4.05], p=0.41), and remission at 12 weeks of followup (OR = 2.06, [95% CI - 0.84, 5.04], p=0.11) did not differ between sertraline (N=67) and placebo (N=64). Sertraline-treated patients experienced more adverse events, most notably gastrointestinal and respiratory, than placebo-treated patients.\n\nInterpretation\nSertraline did not demonstrate efficacy for the treatment depression symptoms in patients with Alzheimer's disease. In addition, its use was associated with an increased incidence of adverse events. Thus, selective serotonin reuptake inhibitors may be of limited value for treating depression in AD patients",
            "publicationTitle": "The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry",
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            "partNumber": "",
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            "pages": "136-145",
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            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Am J Geriatr Psychiatry",
            "DOI": "10.1097/JGP.0b013e3181c796eb",
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            "url": "http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2842121/",
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            "extra": "PMID: 20087081\nPMCID: PMC2842121",
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                    "tag": "Double-Blind Method",
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                {
                    "tag": "Female",
                    "type": 1
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                    "type": 1
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                {
                    "tag": "Male",
                    "type": 1
                },
                {
                    "tag": "Medication Adherence",
                    "type": 1
                },
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                    "tag": "Patient Dropouts",
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                {
                    "tag": "Placebos",
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                    "tag": "Serotonin Uptake Inhibitors",
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