阿尔茨海默病的直立性低血压:脑功能障碍的结果还是原因?

Aging (Milan, Italy) Pub Date : 1999-06-01
A Siennicki-Lantz, B Lilja, S Elmståhl
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引用次数: 0

摘要

在阿尔茨海默病(AD)中,直立测试时发现自主神经功能障碍与大脑额叶灌注不足之间存在关联。为了确定额叶灌注不足是否依赖于血流动力学紊乱的纵向影响,还是促成了这些影响,我们研究了AD晚期直立性低血压(OH)与静息脑血流量(CBF)之间的关系。对12名老年痴呆的阿尔茨海默型(SDAT)女性和15名非痴呆女性(平均年龄82.6岁,SD 3.8 vs 81.8岁,SD 3.5)进行直立试验。12例SDAT患者中的4例和9例对照患者有OH(定义为收缩压下降>或= 20 mmHg)。在静息条件下使用600 Mbq 99mTc HMPAO单光子发射计算机断层扫描(SPECT)测定脑血流,并在与小脑相关的皮质区进行量化。在有SDAT和OH的患者中,额叶和顶额皮质区的CBF低于没有OH的SDAT患者。前一组更年轻,痴呆症持续时间更短。对照组与对照组之间的CBF无显著差异。伴有或不伴有OH的SDAT患者在Berger痴呆量表或Katz' ADL指数中没有观察到差异。关于OH的存在,在SDAT组和对照组中,与自主神经紊乱(腹泻、食欲不振、吞咽困难、眩晕)相关的症状发生率没有差异。我们的结论是,在阿尔茨海默病的过程中,OH可以促进额叶脑的变化,并可能加剧疾病。进一步参与额叶功能障碍加重血压失调的老年人进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Orthostatic hypotension in Alzheimer's disease: result or cause of brain dysfunction?

In Alzheimer's disease (AD), an association was found between autonomic dysfunction and frontal hypoperfusion in brain during orthostatic testing. To ascertain whether frontal hypoperfusion is dependent on longitudinal effects of hemodynamic disturbances, or contributes to them, we studied the relationship between the presence of orthostatic hypotension (OH) and resting cerebral blood flow (CBF) in late stages of AD. Twelve women with senile dementia of Alzheimer type (SDAT), and 15 non-demented women (mean age 82.6 years, SD 3.8 vs 81.8 years, SD 3.5) were examined with the orthostatic test. Four of 12 patients with SDAT, and 9 controls had OH (defined as systolic blood pressure fall > or = 20 mmHg). CBF was determined under resting conditions using 600 Mbq 99mTc HMPAO single photon emission computerized tomography (SPECT), and quantified in cortical areas in relation to cerebellum. In patients with SDAT and OH, CBF was lower in frontal and parieto-frontal cortical areas than in SDAT patients without OH. The former group was younger and had a shorter dementia duration. No significant differences in CBF were observed between controls with vs without OH. No differences in SDAT patients with or without OH were observed in the Berger dementia scale or Katz' ADL index. No difference in incidence of symptoms related to autonomic disturbances (diarrhea, obstipation, dysphagia, vertigo) was observed in either the SDAT or control group with regard to OH presence. We conclude that during the course of AD, OH can contribute to frontal brain changes and may exacerbate the disease. The further involvement of frontal dysfunction in aggravating blood pressure dysregulation in the elderly is discussed.

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