Elevated Soluble TNF-Receptor 1 in the Serum of Predementia Subjects with Cerebral Small Vessel Disease

Biomolecules. 2023 Mar 13;13(3):525. doi: 10.3390/biom13030525.

Abstract

Tumor necrosis factor-receptor 1 (TNF-R1)-mediated signaling is critical to the regulation of inflammatory responses. TNF-R1 can be proteolytically released into systemic blood circulation in a soluble form (sTNF-R1), where it binds to circulating TNF and functions to attenuate TNF-mediated inflammation. Increases of peripheral sTNF-R1 have been reported in both Alzheimer's disease (AD) dementia and vascular dementia (VaD). However, the status of sTNF-R1 in predementia subjects (cognitive impairment, no dementia, CIND) is unknown, and putative associations with cerebral small vessel disease (CSVD), as well as with longitudinal changes in cognitive functions are unclear. We measured baseline serum sTNF-R1 in a longitudinally assessed cohort of 93 controls and 103 CIND, along with neuropsychological evaluations and neuroimaging assessments. Serum sTNF-R1 levels were increased in CIND compared with controls (p < 0.001). Higher baseline sTNF-R1 levels were specifically associated with lacunar infarcts (rate ratio = 6.91, 95% CI 3.19-14.96, p < 0.001), as well as lower rates of cognitive decline in the CIND subgroup. Our data suggest that sTNF-R1 interacts with vascular cognitive impairment in a complex manner at predementia stages, with elevated levels associated with more severe CSVD at baseline, but which may subsequently be protective against cognitive decline.

Keywords: Alzheimer’s disease; TNF-receptor 1; biomarker; cerebral small vessel diseases; predementia; serum; tumor necrosis factor; vascular cognitive impairment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cerebral Small Vessel Diseases*
  • Humans
  • Receptors, Tumor Necrosis Factor
  • Receptors, Tumor Necrosis Factor, Type I*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Receptors, Tumor Necrosis Factor, Type I
  • Receptors, Tumor Necrosis Factor
  • Tumor Necrosis Factor-alpha

Grants and funding

This work was funded by the Singapore National Medical Research Council (grants MOH-000500-01, MOH-000707-01 and MOH-001086-00), the Healthy Longevity Translational Research Programme, Yong Loo Lin School of Medicine (grant HLTRP/2022/PS-01) and the National University Health System (grant A-0006090-00-00). Y.L.C. is a recipient of a post-doctoral fellowship award from the Yong Loo Lin School of Medicine (NUSMED/2021/PDF/05). Research in the laboratory of G.S.D. is supported by the Singapore Ministry of Education (grant MOE2017-T3-1-002).