Risk factors for developing dyskinesia among Parkinson?s disease patients with wearing-off: J-FIRST

被引:3
作者
Mishima, Takayasu [1 ]
Chiu, Shih-Wei [2 ]
Saiki, Hidemoto [3 ,10 ]
Yamaguchi, Takuhiro [2 ]
Shimo, Yasushi [4 ,11 ]
Maeda, Tetsuya [5 ]
Watanabe, Hirohisa [6 ]
Kashihara, Kenichi [7 ]
Nomoto, Masahiro [8 ]
Hattori, Nobutaka [4 ]
Tsuboi, Yoshio [1 ,9 ]
机构
[1] Fukuoka Univ, Fac Med, Dept Neurol, Fukuoka, Japan
[2] Tohoku Univ, Grad Sch Med, Div Biostat, Sendai, Miyagi, Japan
[3] Kitano Hosp, Tazuke Kofukai Med Res Inst, Dept Neurol, Osaka, Japan
[4] Juntendo Univ, Sch Med, Dept Neurol, Tokyo, Japan
[5] Res Inst Brain & Blood Vessels, Dept Neurol, Akita, Japan
[6] Nagoya Univ, Brain & Mind Res Ctr, Nagoya, Aichi, Japan
[7] Okayama Kyokuto Hosp, Dept Neurol, Okayama, Japan
[8] Ehime Univ, Grad Sch Med, Dept Neurol & Clin Pharmacol, Ehime, Japan
[9] 7-45-1 Nanakuma,Johnan Ku, Fukuoka, Fukuoka 8140180, Japan
[10] Aichi Med Univ Hosp, Parkinsons Dis Adv Therapy Ctr, Nagakute, Aichi, Japan
[11] Juntendo Univ, Nerima Hosp, Dept Neurol, Tokyo, Japan
关键词
Dyskinesia; Wearing-off; Quality of life; Nonmotor symptoms; Parkinson?s disease; NONMOTOR SYMPTOMS; MOTOR COMPLICATIONS; LEVODOPA; IMPACT; LIFE; ISTRADEFYLLINE; ZONISAMIDE; FREQUENCY; JAPAN;
D O I
10.1016/j.jns.2023.120619
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Dyskinesia frequently occurs during long-term treatment with levodopa in patients with Parkinson's disease (PD) and impacts quality of life. Few studies have examined risk factors for developing dyskinesia in PD patients exhibiting wearing-off. Therefore, we investigated the risk factors and impact of dyskinesia in PD pa-tients exhibiting wearing-off.Methods: We investigated the risk factors and impact of dyskinesia in a 1-year observational study of Japanese PD patients exhibiting wearing-off (J-FIRST). Risk factors were assessed by logistic regression analyses in patients without dyskinesia at study entry. Mixed-effect models were used to evaluate the impact of dyskinesia on changes in Movement Disorder Society-Unified PD Rating Scale (MDS-UPDRS) Part I and PD Questionnaire (PDQ)-8 scores from one timepoint before dyskinesia was observed.Results: Of 996 patients analyzed, 450 had dyskinesia at baseline, 133 developed dyskinesia within 1 year, and 413 did not develop dyskinesia. Female sex (odds ratio [95% confidence interval]: 2.636 [1.645-4.223]) and administration of a dopamine agonist (1.840 [1.083-3.126]), a catechol-O-methyltransferase inhibitor (2.044 [1.285-3.250]), or zonisamide (1.869 [1.184-2.950]) were independent risk factors for dyskinesia onset. MDS-UPDRS Part I and PDQ-8 scores increased significantly after the onset of dyskinesia (least-squares mean change [standard error] at 52 weeks: 1.11 [0.52], P = 0.0336; 1.53 [0.48], P = 0.0014; respectively).Conclusion: Female sex and administration of a dopamine agonist, a catechol-O-methyltransferase inhibitor, or zonisamide were risk factors for dyskinesia onset within 1 year in PD patients exhibiting wearing-off. Nonmotor symptoms and quality of life deteriorated after dyskinesia onset.
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页数:9
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