Longitudinal trajectories of Alzheimer's disease CSF biomarkers and blood pressure in cognitively healthy subjects

Author:

Biskaduros Adrienne1ORCID,Glodzik Lidia1,Saint Louis Leslie A.1,Rusinek Henry2,Pirraglia Elizabeth3,Osorio Ricardo4,Butler Tracy1,Li Yi1,Xi Ke1,Tanzi Emily1,Harvey Patrick1,Zetterberg Henrik56789,Blennow Kaj561011,de Leon Mony J.1

Affiliation:

1. Brain Health Imaging Institute Department of Radiology Weill Cornell Medicine New York New York USA

2. Department of Radiology New York University Grossman School of Medicine New York New York USA

3. Department of Population Health New York University Grossman School of Medicine New York New York USA

4. Department of Psychiatry New York University Grossman School of Medicine New York New York USA

5. Department of Psychiatry and Neurochemistry University of Gothenburg Mölndal Sweden

6. Clinical Neurochemistry Laboratory Sahlgrenska University Hospital Mölndal Sweden

7. Department of Neurodegenerative Disease UCL Institute of Neurology Queen Square London UK

8. UK Dementia Research Institute at UCL London UK

9. Hong Kong Center for Neurodegenerative Diseases Clear Water Bay Hong Kong China

10. Paris Brain Institute ICM Pitié‐Salpêtrière Hospital Sorbonne University Paris France

11. Neurodegenerative Disorder Research Center Division of Life Sciences and Medicine and Department of Neurology Institute on Aging and Brain Disorders University of Science and Technology of China and First Affiliated Hospital of USTC Hefei P.R. China

Abstract

AbstractINTRODUCTIONWe examined whether hypertension (HTN) was associated with Alzheimer's disease‐related biomarkers in cerebrospinal fluid (CSF) and how changes in blood pressure (BP) related to changes in CSF biomarkers over time.METHODSA longitudinal observation of cognitively healthy normotensive subjects (n = 134, BP < 140/90, with no antihypertensive medication), controlled HTN (n = 36, BP < 140/90, taking antihypertensive medication), and 35 subjects with uncontrolled HTN (BP ≥ 140/90). The follow‐up range was 0.5to15.6 years.RESULTSTotal tau (T‐tau) and phospho‐tau181 (P‐tau 181) increased in all but controlled HTN subjects (group×time interaction: p < 0.05 for both), but no significant Aβ42 changes were seen. Significant BP reduction was observed in uncontrolled HTN, and it was related to increase in T‐tau (p = 0.001) and P‐tau 181 (p < 0.001).DISCUSSIONLongitudinal increases in T‐tau and P‐tau 181 were observed in most subjects; however, only uncontrolled HTN had both markers increase alongside BP reductions. We speculate cumulative vascular injury renders the brain susceptible to relative hypoperfusion with BP reduction.Highlights Over the course of the study, participants with uncontrolled HTN at baseline showed greater accumulation of CSF total tau and phospho‐tau181 (P‐tau 181) than subjects with normal BP or with controlled HTN. In the group with uncontrolled HTN, increases in total tau and P‐tau 181 coincided with reduction in BP. We believe this highlights the role of HTN in vascular injury and suggests decline in cerebral perfusion resulting in increased biomarker concentrations in CSF. Medication use was the main factor differentiating controlled from uncontrolled HTN, indicating that earlier treatment was beneficial for preventing accumulations of pathology.

Funder

National Institutes of Health

Publisher

Wiley

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