Logo

American Heart Association

  208
  0


Final ID: 30

Acute Effects Of Sodium Chloride Or Its Substitute Potassium Chloride On Microvascular Function In Healthy Volunteers

Abstract Body: Dietary high sodium intake is a modifiable risk factors for cardiovascular (CV) diseases including vascular dysfunction and subsequently arteriosclerosis. A partial sodium substitution by potassium is associated with a lower risk of CV events and death. Our aim was to investigate the acute impact of sodium and potassium on retinal microvascular function, an established biomarker for systemic CV risk stratification.
Eighteen male and 27 female healthy individuals (mean age 31years) were randomized to eat a salty soup containing either 9g sodium chloride (high salt group), 6g sodium chloride (intermediate salt group) or 6g sodium chloride plus 3g potassium chloride (substitution group). Microvascular measurements were performed before (t0) as well as four (t4) and 24 hours (t24) after soup intake. Microvascular health was measured by investigating retinal vessel diameters. A higher arteriolar-to-venular diameter ratio (AVR) is associated with improved vascular health. Microvascular endothelial function was quantified by flickerlight-induced retinal arteriolar dilation.
The 9g (139±2mmol/l vs. 141±2mmol/l, p<0.001) and 6g salt group (140±1mmol/l vs. 141±2 mmol/l, p=0.028) had higher serum sodium concentrations at t4 compared to baseline. Serum sodium concentrations of the substitution group showed no significant difference between time points, but a significant increase in serum potassium (3.7±0.3mmol/l vs. 3.9±0.2mmol/l, p=0.019). Microvascular endothelial function was significantly decreased in the high salt group from baseline to t4 (4.5±2.2% vs. 3.7±2.2%, p=0.041), without significant changes in the other groups. In the sodium groups, there was a strong correlation between the increase in serum sodium concentration from t0 to t4 and an impaired endothelial function after t4 (R2=0,255, p=0,005). The substitution group showed improved microvascular health, quantified by higher AVR at t4 compared to t0 (0,83±0,07 vs. 0,86±0,07, p<0,001). An increase in serum sodium was negatively associated with AVR (R2=0,14, p=0,013) whereas an increase in serum potassium was positively correlated with AVR (R2=0,19, p=0,003).
An acute increase in serum sodium is associated with impaired microvascular endothelial function. Replacement of sodium by potassium seems to improve microvascular function already after a single potassium intake. These results might explain the beneficial effects of potassium on CV outcomes as well as the harmful effects of sodium on vascular function.
  • Stock-schrooer, Annika  ( Heinrich-Heine University , Duesseldorf , Germany )
  • Streese, Lukas  ( Heinrich-Heine University , Duesseldorf , Germany )
  • Rammo, Randa  ( Heinrich-Heine University , Duesseldorf , Germany )
  • Kantauskaite, Marta  ( Heinrich-Heine University , Duesseldorf , Germany )
  • Rump, Lars Christian  ( Heinrich-Heine-University , Dusseldorf , Germany )
  • Mueller, Dominik  ( MAX DELBRUCK CTR , Berlin , Germany )
  • Stegbauer, Johannes  ( Heinrich-Heine University , Duesseldorf , Germany )
  • Author Disclosures:
    Annika Stock-Schrooer: No Answer | Lukas Streese: DO NOT have relevant financial relationships | Randa Rammo: No Answer | Marta Kantauskaite: No Answer | Lars Christian Rump: No Answer | Dominik Mueller: DO NOT have relevant financial relationships | Johannes Stegbauer: DO NOT have relevant financial relationships
Meeting Info:
Session Info:

14.A Novel interventions in improving BP control in the digital era

Saturday, 09/07/2024 , 08:00AM - 09:30AM

Oral Abstract Session

More abstracts on this topic:
A Phase 2a randomized controlled trial of once-daily versus twice-daily remote ischemic conditioning in vascular cognitive impairment (TRIC-VCI)

Ganesh Aravind, Mccreary Cheryl, Sahlas Demetrios, Sharma Mukul, Swartz Richard, Smith Eric, Barber Philip, Black Sandra, Corbett Dale, Field Thalia, Frayne Richard, Hachinski Vladimir, Ismail Zahinoor, Mai Lauren

A major uremic toxin indoxyl sulfate impairs macrophage efferocytosis and accelerates atherogenesis: a potential mechanism for cardiovascular risk in chronic kidney disease

Jha Prabhash, Kasai Taku, Vromman Amelie, Holden Rachel, Libby Peter, Tabas Ira, Singh Sasha, Aikawa Elena, Aikawa Masanori, Lupieri Adrien, Sonawane Abhijeet, Le Thanh-dat, Becker-greene Dakota, Chelvanambi Sarvesh, Turner Mandy, Nakamura Yuto, Passos Livia

More abstracts from these authors:
Discovery for Tomorrow's Medicine: Taking Responsibility for Planetary Health

Mueller Dominik

Propionate Attenuates Hypertensive Cardiovascular Damage During Aging

Hahn Milena, Rahman Masudur, Arifaj Denada, Hering Lydia, Rump Lars Christian, Suvorava Tatsiana, Temme Sebastian, Stegbauer Johannes

You have to be authorized to contact abstract author. Please, Login
Not Available