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Effects of Different Forms of a Natural Heart Hormone on Blood Pressure and Fluid Balance in Healthy Volunteers

15 maja 2026 zaktualizowane przez: Peter Fruergaard Andersen

Effects of Glycosylated Atrial Natriuretic Peptide on Blood Pressure and Fluid Balance in Healthy Volunteers

The human heart produces hormones that help regulate blood pressure and fluid balance in the body. One of these hormones is atrial natriuretic peptide (ANP). ANP lowers blood pressure by relaxing blood vessels and increasing urinary excretion by the kidneys.

Previous research has demonstrated that ANP naturally carries a small sugar molecule attached. This sugar moiety is produced endogenously and can modify the biological activity of ANP. When this sugar is present, ANP may affect blood vessels and renal function differently compared with the non-glycosylated form.

The present study examines how this sugar modification alters the physiological effects of ANP. This is achieved by administering ANP, either with or without the attached sugar molecule, via intravenous infusion. The study aims to determine whether glycosylated ANP differs from the native form in its effects on blood pressure and fluid balance.

Przegląd badań

Szczegółowy opis

Introduction Atrial natriuretic peptide (ANP) is a critical component of the natriuretic peptide family and plays a central role in cardiovascular homeostasis. ANP is primarily synthesized and secreted by atrial myocytes in response to atrial stretch and related stimuli. The peptide exerts biological effects through binding to specific receptors, leading to activation of A-type guanylyl cyclase (GC) (also known as NPR-A) and subsequent production of cyclic guanosine monophosphate (cGMP). This signaling cascade induces vasodilation, natriuresis, and diuresis, thereby contributing to regulation of blood pressure and fluid balance.

The concept of proteoforms refers to the various molecular forms that a protein can assume, arising from genetic variation, alternative splicing, and post-translational modification. ANP proteoforms therefore comprise molecular variants of ANP with potentially distinct biological activities and clinical implications.

ANP proteoforms have diagnostic and prognostic value in cardiovascular disease. Elevated ANP and related peptides indicate increased cardiac stress and are observed in conditions such as heart failure, hypertension, and acute coronary syndromes. Measurement of ANP, together with B-type natriuretic peptide (BNP) and N-terminal proBNP (NT-proBNP), is widely used in clinical practice to assist diagnosis and guide management (Volpe 2021).

Beyond diagnostic utility, ANP possesses therapeutic potential. Vasodilatory and natriuretic properties make ANP an attractive candidate for treatment of conditions associated with fluid overload and hypertension. Recombinant ANP analogues have been used clinically in acute heart failure.

Recent advances highlight strategies to enhance natriuretic peptide activity. Inhibition of neprilysin prolongs peptide half-life and biological effect. Combined neprilysin inhibition and angiotensin receptor blockade has demonstrated clinical benefit in heart failure (McMurray 2013).

Post-translational modification, including glycosylation, further diversifies ANP function. Glycosylated ANP refers to peptide forms containing covalently attached carbohydrate groups, typically linked to serine or threonine residues. This modification alters receptor binding, biological activity, and resistance to proteolytic degradation. Glycosylation may therefore influence the physiological and therapeutic profile of ANP. Recent observations suggest that glycosylation modulates interaction with natriuretic peptide receptors and downstream signaling pathways (Hansen 2019).

Objectives, Hypothesis, and Endpoints The primary objective of the study is to clarify the physiological significance of glycosylated ANP in humans.

The primary hypothesis is that glycosylated ANP regulates blood pressure without inducing diuresis.

Primary endpoints include diuresis and natriuresis during intervention. Secondary endpoints include changes in blood pressure and plasma and urinary concentrations of natriuretic peptides, renin-angiotensin-aldosterone parameters, electrolytes, cyclic nucleotides, metabolic substrates, stress hormones, and amino acids.

Methods and Study Design The study is designed as a randomized, double-blind, placebo-controlled crossover investigation. Each participant acts as an individual control. Randomization assigns infusion with ANP, glycosylated ANP (gANP), or saline on separate study days.

Following written informed consent, screening is performed after overnight fasting and includes clinical assessment, laboratory evaluation, and urine testing.

On study days, participants are admitted after a 10-hour fast. Procedures include bladder emptying, venous catheter placement, baseline sampling, and continuous blood pressure monitoring. Infusions of ANP, gANP, or saline are administered according to protocol.

Blood samples are obtained at predefined intervals, and urine is collected during and after infusion. Ultrasonographic assessment of vascular parameters and bladder volumes is performed where applicable.

Study Population Inclusion criteria comprise healthy male individuals aged 18-30 years with normal body mass index and hemoglobin levels.

Exclusion criteria include recent illness, chronic disease, hypotension, smoking, substance abuse, recent blood donation, and medication use incompatible with study requirements.

Safety and Ethics Both ANP and gANP are associated with blood pressure reduction. Continuous monitoring is implemented, and infusion is discontinued if symptomatic hypotension occurs.

The study is conducted in accordance with ethical guidelines, with approval from the relevant ethics committee.

Biobank and Data Handling Biological samples are coded and stored according to regulatory requirements. Analyses are performed at designated institutions, and remaining material is handled in accordance with approved protocols.

Funding and Registration The study is supported by Innovation Fund Denmark. A patent application related to glycosylated ANP has been filed.

Trial registration was completed following recognition of registry requirements, with all study parameters finalized prior to participant enrollment and approved by the ethics committee.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

17

Faza

  • Wczesna faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

      • Copenhagen, Dania, 2400
        • 4) Department of Clinical Pharmacology, Copenhagen University Hospital - Bispebjerg and Frederiksberg, Copenhagen, Denmark

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły

Akceptuje zdrowych ochotników

Tak

Opis

Inclusion Criteria:

  • Healthy male volunteers
  • Age: 18-30 years
  • BMI: 20-25 kg/m²
  • Body weight ≤90 kg (amended protocol)
  • Normal hemoglobin
  • Ability to provide informed consent

Exclusion Criteria:

  • Acute illness within two weeks
  • Chronic cardiovascular, renal, hepatic, pulmonary, metabolic or malignant disease
  • Hypotension or history of syncope
  • Smoking
  • Substance or alcohol abuse
  • Recent blood donation (<3 months)
  • Medication that cannot be safely interrupted

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Podstawowa nauka
  • Przydział: Randomizowane
  • Model interwencyjny: Zadanie krzyżowe
  • Maskowanie: Potroić

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Aktywny komparator: Atrial Natriuretic Peptide (ANP) - a well described cardiac hormone
Atrial Natriuretic Peptide (ANP) Participants receive an intravenous infusion of native atrial natriuretic peptide (ANP), a naturally occurring heart hormone known to lower blood pressure by relaxing blood vessels and increasing salt and water excretion by the kidneys. ANP is administered at a fixed weight-adjusted dose over a defined infusion period, followed by post-infusion observation and monitoring of blood pressure, urine output, and blood markers.

Interventions

Original protocol:

ANP: 200 pmol/kg/min for 120 minutes gANP: 200 pmol/kg/min for 120 minutes

Amended protocol:

ANP: 200 pmol/kg/min for 60 minutes gANP: 300 pmol/kg/min for 60 minutes

Control:

Saline infusion at 0.7 mL/kg/hour

Eksperymentalny: Glycosylated Atrial Natriuretic Peptide (gANP) - a naturally occurring modified cardiac hormone
Participants receive an intravenous infusion of glycosylated atrial natriuretic peptide (gANP), a naturally occurring sugar-modified form of ANP. Glycosylation alters the stability and biological activity of the hormone. gANP is administered at a weight-adjusted dose comparable to or slightly higher than native ANP, according to protocol amendments, with the same monitoring procedures. The purpose is to assess whether the sugar-modified form produces different effects on blood pressure, fluid balance, and vascular function compared with native ANP.

Interventions

Original protocol:

ANP: 200 pmol/kg/min for 120 minutes gANP: 200 pmol/kg/min for 120 minutes

Amended protocol:

ANP: 200 pmol/kg/min for 60 minutes gANP: 300 pmol/kg/min for 60 minutes

Control:

Saline infusion at 0.7 mL/kg/hour

Komparator placebo: Placebo (Saline)
Participants receive an intravenous infusion of isotonic saline at a low, weight-adjusted rate. This arm serves as a placebo control to account for the effects of the infusion procedure, time, and study conditions. The volume administered is equal to both of the active days. All measurements and observations are identical to those performed during the active intervention arms.

Interventions

Original protocol:

ANP: 200 pmol/kg/min for 120 minutes gANP: 200 pmol/kg/min for 120 minutes

Amended protocol:

ANP: 200 pmol/kg/min for 60 minutes gANP: 300 pmol/kg/min for 60 minutes

Control:

Saline infusion at 0.7 mL/kg/hour

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Diuresis and natriuresis
Ramy czasowe: Collection and quantification will take place after completion of two hours of peptide/placebo administration and again after two hours of observation
Primary Objective Diuresis and natriuresis are quantified immediately after conclusion of peptide/placebo administration and repeated after an additional two hours of observation.
Collection and quantification will take place after completion of two hours of peptide/placebo administration and again after two hours of observation

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Blood pressure
Ramy czasowe: Measurement will take place every ten minutes throughout the experimental day.
Blood pressure will be measured during infusion and observation on all experimental days.
Measurement will take place every ten minutes throughout the experimental day.
Metabolic markers
Ramy czasowe: During and after infusion of peptide/placebo with 20-30 min interval.
Metabolic markers in plasma will be quantified (listed in detailed description) in plasma
During and after infusion of peptide/placebo with 20-30 min interval.
cyclic GMP
Ramy czasowe: Quantification will take place once every hour (plasma) and every two hours (urine)
Concentration of the second messenger, cGMP, in plasma and urine.
Quantification will take place once every hour (plasma) and every two hours (urine)

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Główny śledczy: Katrine T-B Schjoldager, Associate Professor, Department of Cellular and Molecular Medicine, University of Copenhagen

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

1 maja 2022

Zakończenie podstawowe (Rzeczywisty)

30 marca 2023

Ukończenie studiów (Rzeczywisty)

30 marca 2026

Daty rejestracji na studia

Pierwszy przesłany

28 kwietnia 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

15 maja 2026

Pierwszy wysłany (Rzeczywisty)

26 maja 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

26 maja 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

15 maja 2026

Ostatnia weryfikacja

1 maja 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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