Plasma Lactate and Incident Hypertension in the Atherosclerosis Risk in Communities Study

BACKGROUND Recent evidence suggests that insufficient oxidative capacity or mitochondrial dysfunction may play a causal role in the development of high blood pressure. However, this hypothesis has not been tested in the general population. We hypothesized that lactate, a measure of oxidative capacit...

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Veröffentlicht in:American journal of hypertension 2015-02, Vol.28 (2), p.216-224
Hauptverfasser: Juraschek, Stephen P., Bower, Julie K., Selvin, Elizabeth, Subash Shantha, Ghanshyam Palamaner, Hoogeveen, Ron C., Ballantyne, Christie M., Young, J. Hunter
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Sprache:eng
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Zusammenfassung:BACKGROUND Recent evidence suggests that insufficient oxidative capacity or mitochondrial dysfunction may play a causal role in the development of high blood pressure. However, this hypothesis has not been tested in the general population. We hypothesized that lactate, a measure of oxidative capacity, would be positively associated with incident hypertension even after accounting for traditional hypertension risk factors. METHODS Plasma lactate was measured in 5,554 participants from the Atherosclerosis Risk in Communities (ARIC) Study with no subclinical or diagnosed hypertension at baseline (1996–1998). Incident hypertension was defined by self-report or hypertension medication use. Analyses were performed with Cox proportional hazards models. RESULTS The mean age was 61.9 years, and the mean lactate was 0.8 mmol/L. During a median follow-up period of 11.9 years (range = 26.9 days to 13.4 years), there were 3,849 new cases of hypertension. The fourth quartile of lactate (compared with the first quartile) was associated with an elevated risk of hypertension (hazard ratio (HR) = 1.18; 95% confidence interval (CI) = 1.07–1.31) even after adjustment for traditional risk factors, including baseline systolic and diastolic blood pressure. This association was stronger when the population was restricted to participants with normal blood pressure (
ISSN:0895-7061
1941-7225
DOI:10.1093/ajh/hpu117