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The use of hypoglycemic drugs in Parkinson's disease: An updated meta-analysis of randomized controlled trials
被引:0
|作者:
Sobral, Milene Vitoria Sampaio
Soares, Victor Goncalves
[2
]
Moreria, Joa Lucas de Magalhaes Leal
[3
]
Rodrigues, Livia Kneipp
[4
]
Rocha, Paula
[5
]
Bendaham, Lucas Cael Azevedo Ramos
[6
]
Goncalves, Ocilio Ribeiro
[7
]
Pirolla, Rafaela da Cunha
[1
]
Vilela, Lucas Veronezi
[1
]
de Abreu, Victoria Stadler
[8
]
Almeida, Kelson James
[7
]
机构:
[1] Univ Western Sao Paulo, Presidente Prudente, Brazil
[2] Fed Univ Jequitinhonha & Mucuri Valleys, Diamantina, Brazil
[3] State Univ Feira De Santana, Feira de Santana, Brazil
[4] Univ Fed Minas Gerais, Belo Horizonte, Brazil
[5] Univ Miami, Miami, FL USA
[6] Univ Fed Roraima, Boa Vista, Brazil
[7] Univ Fed Piaui, Teresina, Brazil
[8] Med Sch Petropolis, Rio De Janeiro, Brazil
关键词:
Parkinson's disease;
Hypoglycemic drugs;
Meta-analysis;
DOUBLE-BLIND;
NEUROPROTECTION;
PIOGLITAZONE;
DIAGNOSIS;
RECEPTOR;
D O I:
10.1016/j.parkreldis.2024.107210
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Introduction: Recent studies have demonstrated an association between hypoglycemic medications and neuroprotective action in neurodegenerative diseases, such as Parkinson's disease (PD). Therefore, in this metaanalysis, our objective was to evaluate the efficacy of these medications, compared to placebo, as diseasemodifying therapy in patients with PD. Methods: We systematically searched PubMed, Embase, and Cochrane for studies comparing the use of hypoglycemic drugs and placebo in patients with PD. Statistical analyses were performed using R Studio 4.3.2. Mean difference (MD) with 95 % confidence intervals (CI) were pooled across trials. Outcomes of interest were change in Movement Disorders Society - Unified Parkinson's Disease Rating Scale (MDS-UPDRS) parts I, II, III, IV, and Parkinson's Disease Questionnaire 39 (PDQ-39). Results: This meta-analysis included six randomized controlled trials (RCT) reporting data on 787 patients. Among them, 480 (61 %) received hypoglycemic drugs. Follow-up ranged from 36 to 61 weeks. At the end of follow-up, improvement in MDS-UPDRS part III score during OFF state occurred when subjects received any hypoglycemic agents at their lowest dose (MD -1.36; 95 % IC -2.78 to -0.47; I2 = 38 %), as well as highest doses (MD -1.58; 95 % IC -3.07 to -0.09; I2 = 50 %). Changes in MDS-UPDRS part III score in patients examined in the ON state who received any dose of any hypoglycemic agents (MD -3.32; 95 % IC -5.28 to -1.36; I2 = 0 %) were significant. There was no significant difference between groups MDS-UPDRS parts I, II, IV, and PDQ-39. Conclusion: In patients with PD, the use of hypoglycemic agents showed efficacy on symptomatic PD treatment with an improvement in MDS-UPDRS part III.
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