Matsuno Hiromasa, Umehara Tadashi, Mimori Masahiro, Ozawa Masakazu, Shiraishi Tomotaka, Onda Asako, Bono Keiko, Omoto Shusaku, Sengoku Renpei, Murakami Hidetomo, Iguchi Yasuyuki
Department of Neurology, The Jikei University School of Medicine, Tokyo, Japan.
Department of Neurology, Daisan Hospital, The Jikei University School of Medicine, 4-11-1 Izumihoncho, Komae-Shi, Tokyo, 201-8601, Japan.
J Neural Transm (Vienna). 2025 Jul 21. doi: 10.1007/s00702-025-02985-1.
Blood pressure variability, white matter brain lesions and degeneration of nigrostriatal dopaminergic neurons may be associated with each other in patients with Parkinson's disease (PD). We examined the coefficient of variation of systolic blood pressure (CV-sBP) in 122 drug-naïve patients with newly diagnosed PD. The association of CV-sBP with degree of white matter hyperintensities and striatal specific binding ratio (SBR) of I-2 carbomethoxy-3-(4-iodophenyl)-N-(3-fluoropropyl) nortropane (I-FP-CIT) were examined taking cardiovascular risk factors into account. The results showed that patients with higher CV-sBP were older (r = 0.362, p < 0.001) and had severer periventricular hyperintensities (PVH) (r = 0.261, p = 0.002), deep and subcortical white matter hyperintensities (DSWMH) (r = 0.237, p = 0.004) and lower striatal SBR (right SBR: r = - 0.269, p = 0.002, left SBR: r = - 0.341, p < 0.001). Patients with severer PVH or DSWMH had lower striatal SBR (PVH: r = - 0.317, p < 0.001, DSWMH: r = - 0.350, p < 0.001). CV-sBP was significantly associated with left striatal SBR (β =-0.264, p = 0.008), especially left caudate SBR (β = - 0.181, p = 0.044) after controlling for age, sex, motor severity, hypertension, diabetes, and DSWMH grade. In conclusion, higher blood pressure variability was associated with greater dopaminergic degeneration in the left striatum, independently of white matter hyperintensity grade. Whether this association reflects dopaminergic neuronal loss or structural alterations in the striatum remains unclear.
在帕金森病(PD)患者中,血压变异性、脑白质病变和黑质纹状体多巴胺能神经元变性可能相互关联。我们检测了122例新诊断的未经药物治疗的PD患者的收缩压变异系数(CV-sBP)。在考虑心血管危险因素的情况下,研究了CV-sBP与白质高信号程度以及[I-2-甲氧羰基-3-(4-碘苯基)-N-(3-氟丙基)去甲托烷(I-FP-CIT)]纹状体特异性结合率(SBR)之间的关联。结果显示,CV-sBP较高的患者年龄较大(r = 0.362,p < 0.001),脑室周围白质高信号(PVH)更严重(r = 0.261,p = 0.002),深部和皮质下白质高信号(DSWMH)更严重(r = 0.237,p = 0.004),纹状体SBR较低(右侧SBR:r = -0.269,p = 0.002,左侧SBR:r = -0.341,p < 0.001)。PVH或DSWMH更严重的患者纹状体SBR较低(PVH:r = -0.317,p < 0.001,DSWMH:r = -0.350,p < 0.001)。在控制年龄、性别、运动严重程度、高血压、糖尿病和DSWMH分级后,CV-sBP与左侧纹状体SBR显著相关(β = -0.264,p = 0.008),尤其是左侧尾状核SBR(β = -0.181,p = 0.044)。总之,较高的血压变异性与左侧纹状体中更严重的多巴胺能变性相关,与白质高信号分级无关。这种关联是否反映了纹状体中多巴胺能神经元的丢失或结构改变仍不清楚。