认知功能未受损成人血压和阿尔茨海默病生物标志物:一项多中心研究

IF 7.8 Q2 BUSINESS
Mariona Osset-Malla, Aitana Martínez-Velasco, Gonzalo Sánchez-Benavides, Mariateresa Buongiorno, Alejandro de la Sierra, Mahnaz Shekari, Carolina Minguillon, Gwendlyn Kollmorgen, Clara Quijano-Rubio, Henrik Zetterberg, Kaj Blennow, David Vállez García, Marc Suárez-Calvet, Juan Domingo Gispert, Oriol Grau-Rivera
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引用次数: 0

摘要

背景:高血压是痴呆的可改变危险因素,可能影响阿尔茨海默病(AD)的病理。了解这种关系对于制定降低痴呆风险的干预措施至关重要。目的:我们研究了认知功能未受损成人脑脊液(CSF)和淀粉样蛋白(Aβ)正电子发射断层扫描(PET)中血压与AD生物标志物之间的横断和纵向关联。设计:前瞻性观察研究。背景:我们分析了来自三个观察性前瞻性欧洲研究的认知功能未受损参与者的数据:ALFA+ (NCT02485730)、EPAD-LCS (NCT02804789)和AMYPAD PNHS (EudraCT: 2018- 002277 -22)。测量:ALFA+参与者有脑脊液生物标志物(脑脊液Aβ42, Aβ40, p-tau181, t-tau)和/或Aβ PET数据。EPAD参与者有CSF生物标志物(CSF Aβ42, p-tau181, t-tau), AMYPAD参与者有Aβ PET数据。所有参与者都有关于糖尿病、高血压药物使用和腰臀比的可用数据。采用多变量线性回归模型分析收缩压(SBP)、舒张压(DBP)和脉压(PP)与脑脊液生物标志物或Aβ PET (Centiloid units, CL)之间的横断面相关性;通过基线和随访之间的δ CL评分来检测纵向关联,以评估Aβ PET随时间的变化。结果:我们纳入了405名来自ALFA+的参与者(平均年龄61.1岁;60%为女性),1104例为EPAD患者(平均年龄64.8岁;女性占59.1%),AMYPAD患者340例(平均年龄71.8岁;女性占60%)。在ALFA+中,舒张压与CSF a - β40 (p = 0.016)和p-tau181 (p = 0.050)呈负相关,而收缩压与CL随时间呈非显著正相关(p = 0.058)。在EPAD中,DBP与CSF a - β42和p-tau181呈负相关(p < 0.001),而PP与CSF a - β42呈正相关(p = 0.024)。在AMYPAD中,收缩压(p = 0.002)和PP (p = 0.003)与基线时的CL呈正相关,舒张压(DBP)也有类似的非显著趋势(p = 0.089)。随着时间的推移,DBP升高(p = 0.042)与CL升高显著相关,收缩压也有类似的无显著趋势(p = 0.072)。我们没有发现血压和脑脊液生物标志物的纵向变化之间的显著关联。结论:在认知功能未受损的个体中,血压升高与Aβ PET积累增加有关。需要进一步的研究来阐明DBP和CSF生物标志物之间负相关的潜在机制,这些生物标志物不能反映典型的AD分子特征。这些发现强调了高血压作为认知能力下降的潜在危险因素的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Blood pressure and Alzheimer's disease biomarkers in cognitively unimpaired adults: a multicenter study.

Background: Hypertension is a modifiable risk factor for dementia, potentially influencing Alzheimer's disease (AD) pathology. Understanding this relationship is essential for developing interventions to reduce dementia risk.

Objectives: We investigated cross-sectional and longitudinal associations between blood pressure and AD biomarkers in cerebrospinal fluid (CSF) and amyloid (Aβ) positron emission tomography (PET) in cognitively unimpaired adults.

Design: Prospective observational study.

Setting: We analyzed data from cognitively unimpaired participants from three observational prospective European studies: ALFA+ (NCT02485730), EPAD-LCS (NCT02804789), and AMYPAD PNHS (EudraCT: 2018-002,277-22).

Measurements: ALFA+ participants had either CSF biomarkers (CSF Aβ42, Aβ40, p-tau181, t-tau) and/or Aβ PET data. EPAD participants had CSF biomarkers (CSF Aβ42, p-tau181, t-tau), and AMYPAD participants had Aβ PET data. All participants had available data about diabetes, use of hypertensive medication, and waist-to-hip ratio. Multivariable linear regression models were used to analyze cross-sectional associations between systolic blood pressure (SBP), diastolic blood pressure (DBP), and pulse pressure (PP) with CSF biomarkers or Aβ PET (Centiloid units, CL); longitudinal associations were tested by means of delta CL scores between baseline and follow-up to assess Aβ PET changes over time.

Results: We included 405 participants from ALFA+ (mean age 61.1 years; 60 % female), 1104 from EPAD (mean age 64.8 years; 59.1 % female), and 340 from AMYPAD (mean age 71.8 years; 60 % female). In ALFA+, DBP was negatively associated with CSF Aβ40 (p = 0.016) and p-tau181 (p = 0.050), while there was a non-significant trend towards a positive association between SBP and CL over time (p = 0.058). In EPAD, DBP was negatively associated with CSF Aβ42 (p < 0.001) and p-tau181 (p = 0.014), while PP was positively associated with CSF Aβ42 (p = 0.024). In AMYPAD, SBP (p = 0.002) and PP (p = 0.003) were positively associated with CL at baseline, with a similar non-significant trend being found for DBP (p = 0.089). Higher DBP (p = 0.042) was significantly associated to increased CL over time, with a similar non-significant trend being found for SBP (p = 0.072). We did not find significant associations between blood pressure and longitudinal changes in CSF biomarkers.

Conclusions: Elevated blood pressure was associated with increased Aβ PET accumulation in cognitively unimpaired individuals. Further research is warranted to elucidate potential mechanisms underlying the negative associations between DBP and CSF biomarkers, which do not reflect the typical AD molecular signature. These findings highlight the relevance of high blood pressure as a potential risk factor for cognitive decline.

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来源期刊
The Journal of Prevention of Alzheimer's Disease
The Journal of Prevention of Alzheimer's Disease Medicine-Psychiatry and Mental Health
CiteScore
9.20
自引率
0.00%
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期刊介绍: The JPAD Journal of Prevention of Alzheimer’Disease will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including: neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes.JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.We hope that JPAD with your contribution will play a role in the development of Alzheimer prevention.
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