Abstract

BackgroundThe metabolic syndrome (MetS) is an established cardiovascular risk factor. Here, we investigated its role in cognitive impairment.MethodsBaseline data from 202 participants (aged 65 to 87 years) of the BioCog study were used. All were free of clinical dementia (MMSE≥24/30). Cognitive impairment was defined as the lowest tertile of a cognitive summary score. Multiple logistic regression analyses examined associations of body mass index (BMI), triglycerides (TG), high-density lipoprotein (HDL-C), glucose and glycated hemoglobin A1c (HbA1c) levels with the odds of cognitive impairment. MetS was defined as ≥3 of its 5 components obesity (BMI ≥ 30 kg/m2), elevated TG (TG ≥1.7 mmol/L), reduced HDL-C (males: < 1.0 mmol/L; females: < 1.3 mmol/L), elevated glucose (glucose ≥5.5 mmol/L and/or diagnosed diabetes) and elevated blood pressure (history of hypertension). Analyses controlled for age, sex and smoking history.ResultsLower HDL-C was significantly associated with a higher odds of cognitive impairment (OR 2.70 per 1 mmol/L reduction; 95% CI 1.25, 5.56; p = 0.011), whereas BMI, TG, glucose and HbA1c were not (all p > 0.05). Results for HDL-C were similar when HDL-C, glucose, BMI and TG were entered into a single model (OR 2.56 per 1 mmol/L reduction, 95% CI 1.09, 5.88, p = 0.031) and when cerebrovascular disease and coronary heart disease were additionally controlled for (OR 2.56 per 1 mmol/L reduction, 95% CI 1.06, 6.25, p = 0.036). Among the 5 MetS components, participants with elevated TG were at 2-fold increased odds of impairment (OR 2.09, 95% CI 1.08, 4.05, p = 0.028) including when the remaining 4 MetS components were entered (OR 2.23, 95% CI 1.07, 4.65, p = 0.033), but the finding was no longer statistically significant when cerebrovascular disease and coronary heart disease were additionally controlled for (p = 0.11). Presence of MetS and of obesity, reduced HDL-C, elevated glucose or elevated blood pressure were not significantly associated with impairment (all p > 0.05).ConclusionOur findings support low HDL-C as an independent risk marker of cognitive impairment in older age. The need for research into mediatory and confounding factors, and re-evaluation of traditional cut-off points is highlighted.Trial registrationThe study was registered on 15th October 2014 at clinicaltrials.gov (NCT02265263).

Highlights

  • The metabolic syndrome (MetS) is an established cardiovascular risk factor

  • MetS has traditionally primarily been linked to cardiovascular disease (CVD), studies suggest that MetS [4,5,6,7] and metabolic abnormalities more generally [7,8,9] may be related to cognitive impairment as a type of organ dysfunction that burdens the global economy to extents similar to CVD [10]

  • We studied the association of the number of abnormal MetS components with the odds of cognitive impairment using 0 abnormal components as reference category

Read more

Summary

Introduction

The metabolic syndrome (MetS) is an established cardiovascular risk factor. Here, we investigated its role in cognitive impairment. The metabolic syndrome (MetS) is a cluster of metabolic abnormalities, including abdominal obesity, elevated blood pressure (BP), elevated blood glucose levels, low high-density lipoprotein cholesterol (HDL-C) levels, and elevated triglyceride (TG) levels, and is suggested to play a major role in the development of cardiovascular disease (CVD) and type 2 diabetes mellitus [1]. MetS [12] and its contributing parameters of metabolic dysfunction (e.g., [13]) are hugely prevalent in Western societies and on a global scale, but all are modifiable. This implies a potential for strategic improvement of public health that warrants clarification. We examined associations of MetS, of each of its 5 components and of associated continuous parameters of metabolic dysfunction with cognitive impairment in a community-based sample of older adults without clinical dementia

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call