Impact of 60 days of head-down bed rest on large arteries.


Journal

Journal of hypertension
ISSN: 1473-5598
Titre abrégé: J Hypertens
Pays: Netherlands
ID NLM: 8306882

Informations de publication

Date de publication:
01 10 2022
Historique:
entrez: 2 9 2022
pubmed: 3 9 2022
medline: 9 9 2022
Statut: ppublish

Résumé

The long-term cardiovascular consequences of microgravity on large arteries are a threat for long-term space missions. We hypothesized that changes in arterial properties differ according to the arterial territory (upper or lower body), and arterial structure (elastic vs. muscular arteries), in response to 60-day head-down bed rest (HDBR). Twenty healthy male volunteers were included and received a daily multivitamin supplementation in a double-blind fashion. At baseline, 29 and 52 days during strict HDBR, then 12 and 30 days after HDBR, aortic stiffness was measured using carotid-to-femoral pulse wave velocity (cf-PWV) and aortic MRI. Carotid, femoral, brachial and popliteal arteries were studied by ultrasound echo tracking, central blood pressure (BP) by tonometry and endothelial function by flow-mediated dilatation. Cf-PWV increased during HDBR (+0.8 and +1.1m/s, at D29 and D52, respectively, P = 0.004), corresponding to an increase in vascular age up to +11 years (P = 0.003). Changes were similar to those observed on MRI (+0.8 m/s at D52, P < 0.01) and were independent of BP and heart rate changes. After HDBR, cf-PWV showed a substantial recovery at R12 but still remained higher than baseline at R30 (+0.8 m/s, P = 0.018), corresponding to +6.5 years of vascular aging (P = 0.018). Thoracic aorta diameter increased significantly (+6%, P = 0.0008). During HDBR, femoral and popliteal arteries showed dimensional changes, leading to femoral inward hypotrophic remodeling (femoral diameter: -12%, P < 0.05; wall cross-sectional area: -25%, P = 0.014) and popliteal inward eutrophic remodeling (popliteal diameter: -25%, P < 0.05; wall cross-sectional area: -3%, P = 0.51). After HDBR, both arterial territories of the leg recovered. We did not observe any significant changes for carotid arteries nor for endothelial function during and after HDBR. Multivitamin supplementation did not affect vascular changes. HDBR was associated with an important increase in aortic stiffness, which did not completely recover 1 month after the end of HDBR. The thoracic aorta and the lower body muscular arteries underwent significant changes in dimensions whereas the common carotid arteries were preserved. These results should raise caution for those exposed to microgravity, real or simulated.

Sections du résumé

BACKGROUND
The long-term cardiovascular consequences of microgravity on large arteries are a threat for long-term space missions. We hypothesized that changes in arterial properties differ according to the arterial territory (upper or lower body), and arterial structure (elastic vs. muscular arteries), in response to 60-day head-down bed rest (HDBR).
METHOD
Twenty healthy male volunteers were included and received a daily multivitamin supplementation in a double-blind fashion. At baseline, 29 and 52 days during strict HDBR, then 12 and 30 days after HDBR, aortic stiffness was measured using carotid-to-femoral pulse wave velocity (cf-PWV) and aortic MRI. Carotid, femoral, brachial and popliteal arteries were studied by ultrasound echo tracking, central blood pressure (BP) by tonometry and endothelial function by flow-mediated dilatation.
RESULTS
Cf-PWV increased during HDBR (+0.8 and +1.1m/s, at D29 and D52, respectively, P = 0.004), corresponding to an increase in vascular age up to +11 years (P = 0.003). Changes were similar to those observed on MRI (+0.8 m/s at D52, P < 0.01) and were independent of BP and heart rate changes. After HDBR, cf-PWV showed a substantial recovery at R12 but still remained higher than baseline at R30 (+0.8 m/s, P = 0.018), corresponding to +6.5 years of vascular aging (P = 0.018). Thoracic aorta diameter increased significantly (+6%, P = 0.0008). During HDBR, femoral and popliteal arteries showed dimensional changes, leading to femoral inward hypotrophic remodeling (femoral diameter: -12%, P < 0.05; wall cross-sectional area: -25%, P = 0.014) and popliteal inward eutrophic remodeling (popliteal diameter: -25%, P < 0.05; wall cross-sectional area: -3%, P = 0.51). After HDBR, both arterial territories of the leg recovered. We did not observe any significant changes for carotid arteries nor for endothelial function during and after HDBR. Multivitamin supplementation did not affect vascular changes. HDBR was associated with an important increase in aortic stiffness, which did not completely recover 1 month after the end of HDBR. The thoracic aorta and the lower body muscular arteries underwent significant changes in dimensions whereas the common carotid arteries were preserved.
CONCLUSION
These results should raise caution for those exposed to microgravity, real or simulated.

Identifiants

pubmed: 36052527
doi: 10.1097/HJH.0000000000003235
pii: 00004872-202210000-00022
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2058-2067

Informations de copyright

Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.

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Auteurs

Pierre Boutouyrie (P)

Service de Pharmacologie Clinique, Hôpital Européen Georges Pompidou (APHP).
Unité INSERM U970, PARCC INSERM.
Université de Paris.

Antoine Fayol (A)

Service de Pharmacologie Clinique, Hôpital Européen Georges Pompidou (APHP).
Unité INSERM U970, PARCC INSERM.
Université de Paris.
Centre d'investigation Clinique - CHU Européen Georges Pompidou (APHP), Paris, France.

Catherine Fortier (C)

Service de Pharmacologie Clinique, Hôpital Européen Georges Pompidou (APHP).
Unité INSERM U970, PARCC INSERM.

Hakim Khettab (H)

Service de Pharmacologie Clinique, Hôpital Européen Georges Pompidou (APHP).
Unité INSERM U970, PARCC INSERM.
Université de Paris.

Catalin Cristian (C)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Helmholtz Institute, Medical Faculty, RWTH Aachen University, Aachen, Germany.

Umit Gencer (U)

Unité INSERM U970, PARCC INSERM.
Service de Radiologie - CHU Européen Georges Pompidou (APHP), Paris, France.

David Fouassier (D)

Centre d'investigation Clinique - CHU Européen Georges Pompidou (APHP), Paris, France.

Elie Mousseaux (E)

Unité INSERM U970, PARCC INSERM.
Service de Radiologie - CHU Européen Georges Pompidou (APHP), Paris, France.

Audrey Derobertmasure (A)

Service de Pharmacologie Clinique, Hôpital Européen Georges Pompidou (APHP).
Unité INSERM U970, PARCC INSERM.
Université de Paris.

Carole Leguy (C)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Helmholtz Institute, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Institute of Measurement Engineering and Sensor Technology, University of Applied Sciences Ruhr West, Mülheim an der Ruhr, Germany.

Rosa-Maria Bruno (RM)

Service de Pharmacologie Clinique, Hôpital Européen Georges Pompidou (APHP).
Unité INSERM U970, PARCC INSERM.
Université de Paris.

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