Author
Listed:
- Amanda Vale-Lira
(Rehabilitation Sciences Program, University of Brasília, Brasília 72220-275, Brazil
These authors contributed equally to this work.)
- Natália Turri-Silva
(Health and Technologies in Health Sciences Program, University of Brasília, Brasília 72220-275, Brazil
BIOMED-REVAL (Rehabilitation Research Centre), Faculty of Rehabilitation Sciences, Hasselt University, 3590 Hasselt, Belgium
These authors contributed equally to this work.)
- Kenneth Verboven
(BIOMED-REVAL (Rehabilitation Research Centre), Faculty of Rehabilitation Sciences, Hasselt University, 3590 Hasselt, Belgium)
- João Luiz Quagliotti Durigan
(Rehabilitation Sciences Program, University of Brasília, Brasília 72220-275, Brazil
Health and Technologies in Health Sciences Program, University of Brasília, Brasília 72220-275, Brazil)
- Alexandra Corrêa G. B. de Lima
(Health and Technologies in Health Sciences Program, University of Brasília, Brasília 72220-275, Brazil)
- Martim Bottaro
(Faculty of Physical Education, University of Brasília, Brasília 70910-900, Brazil)
- Gaspar R. Chiappa
(Human Movement and Rehabilitation Graduate Program, Universidade Evangélica de Goiás, Anápolis 76385-608, Brazil)
- Dominique Hansen
(BIOMED-REVAL (Rehabilitation Research Centre), Faculty of Rehabilitation Sciences, Hasselt University, 3590 Hasselt, Belgium
Heart Centre Hasselt, Jessa Hospital, 3500 Hasselt, Belgium)
- Gerson Cipriano
(Rehabilitation Sciences Program, University of Brasília, Brasília 72220-275, Brazil
Health and Technologies in Health Sciences Program, University of Brasília, Brasília 72220-275, Brazil)
Abstract
Exercise intolerance, a hallmark of patients with heart failure (HF), is associated with muscle weakness. However, its causative microcirculatory and muscle characteristics among those with preserved or reduced ejection fraction (HFpEF or HFrEF) phenotype is unclear. The musculoskeletal abnormalities that could result in impaired peripheral microcirculation are sarcopenia and muscle strength reduction in HF, implying lowered oxidative capacity and perfusion affect transport and oxygen utilization during exercise, an essential task from the microvascular muscle function. Besides that, skeletal muscle microcirculatory abnormalities have also been associated with exercise intolerance in HF patients who also present skeletal muscle myopathy. This cross-sectional study aimed to compare the muscle microcirculation dynamics via near-infrared spectroscopy (NIRS) response during an isokinetic muscle strength test and ultrasound-derived parameters (echo intensity was rectus femoris muscle, while the muscle thickness parameter was measured on rectus femoris and quadriceps femoris) in heart failure patients with HFpEF and HFrEF phenotypes and different functional severities (Weber Class A, B, and C). Twenty-eight aged-matched patients with HFpEF ( n = 16) and HFrEF ( n = 12) were assessed. We found phenotype differences among those with Weber C severity, with HFrEF patients reaching lower oxyhemoglobin (O 2 Hb, μM) (−10.9 ± 3.8 vs. −23.7 ± 5.7, p = 0.029) during exercise, while HFpEF reached lower O 2 Hb during the recovery period (−3.0 ± 3.4 vs. 5.9 ± 2.8, p = 0.007). HFpEF with Weber Class C also presented a higher echo intensity than HFrEF patients (29.7 ± 8.4 vs. 15.1 ± 6.8, p = 0.017) among the ultrasound-derived variables. Our preliminary study revealed more pronounced impairments in local microcirculatory dynamics in HFpEF vs. HFrEF patients during a muscle strength exercise, combined with muscle-skeletal abnormalities detected via ultrasound imaging, which may help explain the commonly observed exercise intolerance in HFpEF patients.
Suggested Citation
Amanda Vale-Lira & Natália Turri-Silva & Kenneth Verboven & João Luiz Quagliotti Durigan & Alexandra Corrêa G. B. de Lima & Martim Bottaro & Gaspar R. Chiappa & Dominique Hansen & Gerson Cipriano, 2022.
"Muscle-Skeletal Abnormalities and Muscle Oxygenation during Isokinetic Strength Exercise in Heart Failure with Preserved Ejection Fraction Phenotype: A Cross-Sectional Study,"
IJERPH, MDPI, vol. 19(2), pages 1-25, January.
Handle:
RePEc:gam:jijerp:v:19:y:2022:i:2:p:709-:d:720732
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:gam:jijerp:v:19:y:2022:i:2:p:709-:d:720732. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: MDPI Indexing Manager (email available below). General contact details of provider: https://www.mdpi.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.