» Articles » PMID: 35983864

Periventricular Rather Than Deep White Matter Hyperintensities Mediate Effects of Hypertension on Cognitive Performance in the Population-based 1000BRAINS Study

Abstract

Objectives: White matter hyperintensities (WMH) of presumed vascular origin are frequent in cerebral MRI of older people. They represent a sign of small vessel disease, are promoted by arterial hypertension, and relate to cognitive deficits. The interdependence of blood pressure and its treatment, WMH, and cognitive performance has not systematically been studied in population-based studies.

Methods: Consequently, we analysed the interdependence of SBP, DBP, and antihypertensive medications, as well as BP/treatment category, with WMH and cognitive performance in 560 participants of the population-based 1000BRAINS study.

Results: BP, its treatment, and BP/treatment category were moderately associated with cognitive performance (e.g. unadjusted β  = -0.10, 95%CI = -0.19 to -0.02 for the association of SBP (per standard deviation of 17.2 mmHg) with global cognition (per standard deviation of 0.5 z score)]. The harmful effect of BP on cognition was strongly mediated by periventricular hyperintensities (PVH), which were significantly associated with both SBP [ β  = 0.24, 95% CI = 0.14-0.34 (per 1-point-increase in Fazekas score)] and global cognition ( β  = -0.22, 95%CI =  -0.32 to -0.13). Thus, PVH mediated as much as 52% of the effects of SBP on cognitive performance. Mediation was less strong for deep white matter hyperintensities (DWMH, 16%), which showed less association with SBP ( β  = 0.14, 95% CI = 0.05-0.24) and global cognition ( β  = -0.12, 95%CI = -0.21 to -0.03). Regarding different cognitive domains, PVH most strongly mediated effects of SBP on nonverbal memory (94%) and executive function (81%).

Conclusion: Our results indicate that PVH may predispose to cognitive impairment associated with hypertension, especially in the domains of nonverbal memory and executive function.

Citing Articles

The genetic and environmental etiology of novel frequency-driven regional parcellations of abnormal white matter.

Lin S, Gillespie N, Notestine R, Gamst A, Chen A, McEvoy L Am J Med Genet B Neuropsychiatr Genet. 2024; 198(1):e33004.

PMID: 39148448 PMC: 11684400. DOI: 10.1002/ajmg.b.33004.


Identifying sources of bias when testing three available algorithms for quantifying white matter lesions: BIANCA, LPA and LGA.

Miller T, Bittner N, Moebus S, Caspers S Geroscience. 2024; 47(1):1221-1237.

PMID: 39115640 PMC: 11872996. DOI: 10.1007/s11357-024-01306-w.


Serum albumin and white matter hyperintensities.

Zahr N, Pfefferbaum A Transl Psychiatry. 2024; 14(1):233.

PMID: 38824150 PMC: 11144249. DOI: 10.1038/s41398-024-02953-5.


Migraine or any headaches and white matter hyperintensities and their progression in women and men.

Schramm S, Tenhagen I, Jokisch M, Gronewold J, Moebus S, Caspers S J Headache Pain. 2024; 25(1):78.

PMID: 38745272 PMC: 11094904. DOI: 10.1186/s10194-024-01782-7.


Distinct patterns of voxel- and connection-based white matter hyperintensity distribution and associated factors in early-onset and late-onset Alzheimer's disease.

Hong H, Chen Y, Liu W, Luo X, Zhang M Alzheimers Dement (Amst). 2024; 16(2):e12585.

PMID: 38651161 PMC: 11033836. DOI: 10.1002/dad2.12585.