Plasma Pro‐Enkephalin A and Incident Cognitive Impairment: The Reasons for Geographic and Racial Differences in Stroke Cohort

Author:

Short Samuel A. P.1ORCID,Wilkinson Katherine2ORCID,Schulte Janin3ORCID,Renteria Miguel Arce4ORCID,Cheung Katharine L.25ORCID,Nicoli Charles D.6,Howard Virginia J.7ORCID,Cushman Mary25ORCID

Affiliation:

1. Larner College of Medicine University of Vermont Burlington VT USA

2. Department of Pathology and Laboratory Medicine, Larner College of Medicine University of Vermont Burlington VT USA

3. SphingoTec GmbH Hennigsdorf Germany

4. Taub Institute for Research on Alzheimer’s Disease and the Aging Brain, Department of Neurology Columbia University College of Physicians and Surgeons New York NY USA

5. Department of Medicine, Larner College of Medicine University of Vermont Burlington VT USA

6. Department of Medicine Walter Reed National Military Medical Center Bethesda MD USA

7. Department of Epidemiology, School of Public Health University of Alabama at Birmingham Birmingham AL USA

Abstract

Background Cardiovascular disease is a risk factor for cognitive impairment. Evidence links both lower and higher concentration of the circulating opioid pro‐enkephalin A (PENK‐A) with stroke risk. We studied the association of plasma PENK‐A with incident cognitive impairment. Methods and Results REGARDS (Reasons for Geographic and Racial Differences in Stroke) is a prospective cohort study of 30 239 adults enrolled from 2003 to 2007. Baseline PENK‐A was measured in a nested case–control study of 462 participants who developed cognitive impairment over 4.7 years, and 556 controls. Logistic regression and spline plots adjusted for confounders estimated odds ratios (ORs) of cognitive impairment by baseline PENK‐A. Interaction terms tested for differences in associations by age, sex, and race. Baseline PENK‐A was comparable between cases and controls. There were significant differences in the association of PENK‐A with cognitive impairment by sex and age (adjusted P =0.003 and 0.06, respectively). In women but not men, spline plots showed that higher and lower PENK‐A were associated with decreased odds of cognitive impairment (ORs for 10th and 90th percentiles versus median, 0.65 [95% CI, 0.43–0.96] and 0.64 [95% CI, 0.41–0.99]), with no difference by age. In men ≥65 years of age but not younger men, higher PENK‐A was associated with decreased odds for cognitive impairment (OR for fourth versus first quartile 0.47 [95% CI, 0.22–0.99]); this pattern was not confirmed with spline plotting. Conclusions High and low levels of circulating opioid PENK‐A were associated with decreased odds of future cognitive impairment in specific subgroups. Additional research is warranted to understand the biology underlying this association and the observed differences by sex.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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