Do prescription stimulants increase risk of Parkinson's disease among adults with attention-deficit hyperactivity disorder? A retrospective cohort study.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-08-14 DOI:10.1093/fampra/cmac153
Hailey M Kindt, Wen-Jan Tuan, Curtis W Bone
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Abstract

Background: Parkinson's disease (PD) is a common neurodegenerative disorder in older adults that is associated with neuroinflammation, oxidative stress, and characterized by loss of dopaminergic cells. Illicit stimulants increase oxidative stress and are associated with increased risk of PD. Prescription stimulants are similar in mechanism to illicit stimulants, yet their influence on PD is not well described. This study aims to determine if prescription stimulants influence risk of PD among older adults with attention-deficit and hyperactivity disorder (ADHD).

Methods: We implemented a retrospective observational cohort design utilizing the TriNetX database which sources from the electronic health records of 57 healthcare organizations. Inclusion criteria were ADHD diagnosis and age ≥50. Those exposed to stimulants and the unexposed controls were matched based on demographics and known risk factors for PD. The outcome of interest was the incidence of PD over a 30-year follow-up period. We utilized TriNetX software for hazard ratio (HR) analysis.

Results: Among the 59,471 individuals treated with prescription stimulants 131 of them developed PD, and there were 272 individuals who developed PD that were not prescribed stimulants. This analysis yielded a HR of 0.419 (HR = 0.419 [95% CI 0.34, 0.516], P = 0.0013).

Conclusion: Illicit stimulants are associated with increased risk of PD, but this study suggests prescribed stimulants may not impart that same risk. The reduced risk in this cohort may be due to protection from illicit substance use and oxidative stress, however additional study exploring the relationship between prescription stimulants and PD is warranted.

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处方兴奋剂会增加注意力缺陷多动障碍成人罹患帕金森病的风险吗?一项回顾性队列研究。
背景:帕金森病(PD)是老年人常见的神经退行性疾病,与神经炎症、氧化应激有关,以多巴胺能细胞的丧失为特征。非法兴奋剂会增加氧化应激,并与帕金森氏症风险增加有关。处方兴奋剂的作用机制与非法兴奋剂相似,但它们对帕金森病的影响尚未得到很好的描述。本研究旨在确定处方兴奋剂是否会影响患有注意力缺陷和多动障碍(ADHD)的老年人罹患帕金森病的风险:我们利用来自 57 家医疗机构电子健康记录的 TriNetX 数据库,采用回顾性观察队列设计。纳入标准为确诊为多动症且年龄≥50岁。暴露于兴奋剂的患者和未暴露于兴奋剂的对照组根据人口统计学特征和已知的帕金森病风险因素进行配对。我们关注的结果是 30 年随访期间的髓鞘脱垂症发病率。我们使用 TriNetX 软件进行了危险比 (HR) 分析:结果:在接受处方兴奋剂治疗的 59471 人中,有 131 人患上了帕金森病,另有 272 人未接受处方兴奋剂治疗但患上了帕金森病。该分析得出的HR值为0.419(HR = 0.419 [95% CI 0.34, 0.516], P = 0.0013):结论:非法兴奋剂与帕金森病风险增加有关,但本研究表明处方兴奋剂可能不会带来同样的风险。该队列中风险降低的原因可能是使用非法药物和氧化应激的保护作用,但还需要进一步研究处方兴奋剂与帕金森病之间的关系。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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