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Procalcitonin and the inflammatory response to salt in essential hypertension: a randomized cross-over clinical trial.

Journal of hypertension
July 1, 2013
Francesca Mallamaci et al. (6 authors)
Journal ArticleRandomized Controlled TrialHuman StudyClinical
Study Details

Study Goal

The researchers aimed to assess the effect of a short-term low-salt diet on biomarkers of innate immunity and inflammation in hypertensive patients.

Results Summary

A very low salt diet increased pro-inflammatory biomarkers (PCT and TNF-α) and decreased the anti-inflammatory cytokine ADPN, with no difference between salt-sensitive and salt-resistant patients.

Population

32 uncomplicated essential hypertensive patients

Effective Dosage

10-20 mmol sodium diet with sodium tablets (180 mEq/day) to achieve 200 mmol intake per day

Duration

2 weeks per intervention

Interactions

None mentioned

Extracted Claims (6)
InterventionDirectionEndpointPopulationDosageImpactClaim #
low-salt diet
increase
procalcitonin (PCT)
essential hypertensive patients
+33%
rose
#1
low-salt diet
increase
tumor necrosis factor-α (TNF-α)
essential hypertensive patients
9%
rose
#2
low-salt diet
decrease
adiponectin (ADPN)
essential hypertensive patients
-17%
underwent an opposite change
#3
low-salt diet
increase
PCT and TNF-α
essential hypertensive patients
-
generates a pro-inflammatory phenotype characterized by an increase
#4
low-salt diet
decrease
ADPN
essential hypertensive patients
-
generates a pro-inflammatory phenotype characterized by an opposite effect
#5
low-salt diet
no change
Changes in inflammation biomarkers
salt-sensitive and salt-resistant patients
-
did not differ
#6
Abstract

OBJECTIVES: Inflammation is considered as a major effector of arterial damage brought about by salt excess in animal models. In a randomized, single masked, cross-over study in 32 uncomplicated essential hypertensive patients, we assessed the effect of a short-term low-salt diet on biomarkers of innate immunity [procalcitonin (PCT), interleukin-6, C-reactive protein, and tumor necrosis factor-α (TNF-α)], adiponectin (ADPN, an anti-inflammatory cytokine), and leptin. METHODS: Patients were randomized to either a 10-20 mmol sodium diet and sodium tablets (180 mEq/day) to achieve a 200 mmol intake per day or the same diet and identical placebo tablets, each for 2 weeks. At the end of each of these periods, all patients underwent a 24-h urine collection, a fasting blood sampling, and a 24 h ambulatory blood pressure monitoring. RESULTS: In parallel with expected increase in plasma renin activity and aldosterone (P<0.001), both PCT (+33%) and TNF-α (9%) rose at low salt intake (P≤0.007) while ADPN underwent an opposite change (- 17%, P<0.001). In a linear regression analysis for repeated measurements, PCT was significantly and inversely related to urinary salt (weighted r=-0.27, P=0.03). Changes in inflammation biomarkers did not differ in salt-sensitive (n=7) and salt-resistant (n=25) patients. CONCLUSION: In essential hypertensive patients, a very low salt diet generates a pro-inflammatory phenotype characterized by an increase in PCT and TNF-α and an opposite effect on an anti-inflammatory cytokine like ADPN.

Medical Subject Headings (MeSH)
AldosteroneBiomarkersCalcitoninCalcitonin Gene-Related PeptideCross-Over StudiesHumansHypertensionInflammationPlacebosProtein PrecursorsReninSingle-Blind MethodSodium Chloride, Dietary
Study Links
Quality Scores
Safety60
Efficacy75/10
Quality85/10
Citation Metrics
Total Citations18
Citations/Year1.5
Relative Citation Ratio0.61
NIH Percentile32.9%
Research Impact Scores
APT Score0.75
Weight Score1.57
Normalized Score0.71
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