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<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">CNR</journal-id><journal-title-group><journal-title>Clinical Neuroscience Research</journal-title></journal-title-group><issn>3083-4899</issn><eissn>2981-8133</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26689/cnr.v1i2.5306</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Effect Evaluation of Madopar Combined with Pramipexole in the Treatment of Parkinson’s Patients</title><url>https://artdesignp.com/journal/CNR/1/2/10.26689/cnr.v1i2.5306</url><author>LiuJianhua,WangChuanqi,TanYu</author><pub-date pub-type="publication-year"><year>2023</year></pub-date><volume>1</volume><issue>2</issue><history><date date-type="pub"><published-time>2023-09-27</published-time></date></history><abstract>Objective: To analyze the clinical efficacy of Madopar combined with pramipexole in the treatment of Parkinson’s disease. Methods: This study was conducted from January 2021 to January 2023. This study involved 80 patients who were divided into two groups using a computerized randomization. The control group received pramipexole and the experimental group received both madopar and pramipexole. The treatment outcomes of these two groups were compared and analyzed. Results: The efficacy of the treatment received in the experimental group was 95.00%, which was higher than that of the control group (77.50%), whereas the total adverse reaction rate of the experimental group was 12.50%, which was lower than that of the control group, 35.00%; the difference was significant (P &amp;lt; 0.05). There was no difference in the levels of tumor necrosis factor α (TNF-α), interleukin 6 (IL-6), C-reactive protein (CRP), miR-124, miR-137, and Unified Parkinson’s Disease Rating Scale (UPDRS) total score (UPDRS Ⅱ, UPDRS Ⅲ, and UPDRS Ⅳ scores) between the control group and the experimental group (P &amp;gt; 0.05). After treatment, these indicators were significantly improved in the experimental group compared to the control group. Conclusion: Madopar combined with pramipexole in the treatment of Parkinson’s is both effective and safe. It delays the progression of the disease and has broad application prospects.</abstract><keywords/></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>Sun Q, Wang Y, Ji Z, et al., 2022, Efficacy and Safety Analysis of Duloxetine Combined with Pramipexole in Patients with Parkinson’s Disease and Depression. International Journal of Psychiatry, 49(6): 1021–1023 + 1027.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B2" content-type="article"><label>2</label><element-citation publication-type="journal"><p>Zheng H, Bei N, Tang Q, et al., 2022, The Effect of Pramipexole Hydrochloride Combined with Hyperbaric Oxygen Chamber Therapy on ?-GABA and Glu in Patients with Parkinson’s Sleep Disorder. 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