Post-walking exercise skeletal muscle perfusion and energetics in patients with symptomatic lower extremity peripheral artery disease
The pathophysiology of symptoms and reduced exercise capacity from peripheral artery disease (PAD) remains unclear. Additionally, there is limited information on blood flow and skeletal muscle energetics after walking exercise in patients with claudication in comparison to healthy individuals. We pr...
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Published in | Journal of nuclear cardiology Vol. 46; p. 102143 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
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Elsevier Inc
01.04.2025
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Abstract | The pathophysiology of symptoms and reduced exercise capacity from peripheral artery disease (PAD) remains unclear. Additionally, there is limited information on blood flow and skeletal muscle energetics after walking exercise in patients with claudication in comparison to healthy individuals.
We prospectively enrolled 19 patients with claudication from PAD and 12 healthy subjects. All participants underwent rest and post-exercise perfusion imaging of the lower leg muscles via PET/CT. Participants exercised on a treadmill following the Gardner-Skinner protocol. Skeletal muscle blood flow (SMBF) was quantified in each leg at rest and immediately after exercise. Phosphocreatine (PCr) recovery and NAD+/NADH concentrations were measured pre- and post-exercise by 31P magnetic resonance spectroscopy (MRS) in a subset of participants. Comparisons were made between the legs of healthy subjects and the asymptomatic and symptomatic legs of patients with PAD.
SMBF increased post-exercise in all participants. Among patients with PAD, the post-exercise/rest SMBF ratio, was higher in the symptomatic (n = 25) than asymptomatic (n = 13) legs (8.03 ± 2.84 vs 6.03 ± 2.81, P = 0.046) and higher than the post-exercise/rest SMBF ratio measured in the legs of healthy subjects (4.40 ± 1.47, P < 0.001). The post-exercise/rest PCr and NAD+/NADH ratios were lower in the legs of patients with PAD (n = 3) when compared with the legs of healthy subjects (n = 6) (0.79 ± 0.06 vs 1.00 ± 0.07 (P = 0.004) and 1.15 ± 0.43 vs 2.08 ± 0.30 (P = 0.007), respectively).
SMBF increased post-exercise to the greatest degree in the symptomatic legs of patients with PAD and post-exercise skeletal muscle mitochondrial function was abnormal in patients with PAD. These data suggest that the causes of symptoms and reduced exercise capacity from PAD are not limited to abnormal perfusion pressure in the legs.
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AbstractList | The pathophysiology of symptoms and reduced exercise capacity from peripheral artery disease (PAD) remains unclear. Additionally, there is limited information on blood flow and skeletal muscle energetics after walking exercise in patients with claudication in comparison to healthy individuals.BACKGROUNDThe pathophysiology of symptoms and reduced exercise capacity from peripheral artery disease (PAD) remains unclear. Additionally, there is limited information on blood flow and skeletal muscle energetics after walking exercise in patients with claudication in comparison to healthy individuals.We prospectively enrolled 19 patients with claudication from PAD and 12 healthy subjects. All participants underwent rest and post-exercise perfusion imaging of the lower leg muscles via PET/CT. Participants exercised on a treadmill following the Gardner-Skinner protocol. Skeletal muscle blood flow (SMBF) was quantified in each leg at rest and immediately after exercise. Phosphocreatine (PCr) recovery and NAD+/NADH concentrations were measured pre- and post-exercise by 31P magnetic resonance spectroscopy (MRS) in a subset of participants. Comparisons were made between the legs of healthy subjects and the asymptomatic and symptomatic legs of patients with PAD.METHODSWe prospectively enrolled 19 patients with claudication from PAD and 12 healthy subjects. All participants underwent rest and post-exercise perfusion imaging of the lower leg muscles via PET/CT. Participants exercised on a treadmill following the Gardner-Skinner protocol. Skeletal muscle blood flow (SMBF) was quantified in each leg at rest and immediately after exercise. Phosphocreatine (PCr) recovery and NAD+/NADH concentrations were measured pre- and post-exercise by 31P magnetic resonance spectroscopy (MRS) in a subset of participants. Comparisons were made between the legs of healthy subjects and the asymptomatic and symptomatic legs of patients with PAD.SMBF increased post-exercise in all participants. Among patients with PAD, the post-exercise/rest SMBF ratio, was higher in the symptomatic (n = 25) than asymptomatic (n = 13) legs (8.03 ± 2.84 vs 6.03 ± 2.81, P = 0.046) and higher than the post-exercise/rest SMBF ratio measured in the legs of healthy subjects (4.40 ± 1.47, P < 0.001). The post-exercise/rest PCr and NAD+/NADH ratios were lower in the legs of patients with PAD (n = 3) when compared with the legs of healthy subjects (n = 6) (0.79 ± 0.06 vs 1.00 ± 0.07 (P = 0.004) and 1.15 ± 0.43 vs 2.08 ± 0.30 (P = 0.007), respectively).RESULTSSMBF increased post-exercise in all participants. Among patients with PAD, the post-exercise/rest SMBF ratio, was higher in the symptomatic (n = 25) than asymptomatic (n = 13) legs (8.03 ± 2.84 vs 6.03 ± 2.81, P = 0.046) and higher than the post-exercise/rest SMBF ratio measured in the legs of healthy subjects (4.40 ± 1.47, P < 0.001). The post-exercise/rest PCr and NAD+/NADH ratios were lower in the legs of patients with PAD (n = 3) when compared with the legs of healthy subjects (n = 6) (0.79 ± 0.06 vs 1.00 ± 0.07 (P = 0.004) and 1.15 ± 0.43 vs 2.08 ± 0.30 (P = 0.007), respectively).SMBF increased post-exercise to the greatest degree in the symptomatic legs of patients with PAD and post-exercise skeletal muscle mitochondrial function was abnormal in patients with PAD. These data suggest that the causes of symptoms and reduced exercise capacity from PAD are not limited to abnormal perfusion pressure in the legs.CONCLUSIONSSMBF increased post-exercise to the greatest degree in the symptomatic legs of patients with PAD and post-exercise skeletal muscle mitochondrial function was abnormal in patients with PAD. These data suggest that the causes of symptoms and reduced exercise capacity from PAD are not limited to abnormal perfusion pressure in the legs. The pathophysiology of symptoms and reduced exercise capacity from peripheral artery disease (PAD) remains unclear. Additionally, there is limited information on blood flow and skeletal muscle energetics after walking exercise in patients with claudication in comparison to healthy individuals. We prospectively enrolled 19 patients with claudication from PAD and 12 healthy subjects. All participants underwent rest and post-exercise perfusion imaging of the lower leg muscles via PET/CT. Participants exercised on a treadmill following the Gardner-Skinner protocol. Skeletal muscle blood flow (SMBF) was quantified in each leg at rest and immediately after exercise. Phosphocreatine (PCr) recovery and NAD+/NADH concentrations were measured pre- and post-exercise by 31P magnetic resonance spectroscopy (MRS) in a subset of participants. Comparisons were made between the legs of healthy subjects and the asymptomatic and symptomatic legs of patients with PAD. SMBF increased post-exercise in all participants. Among patients with PAD, the post-exercise/rest SMBF ratio, was higher in the symptomatic (n = 25) than asymptomatic (n = 13) legs (8.03 ± 2.84 vs 6.03 ± 2.81, P = 0.046) and higher than the post-exercise/rest SMBF ratio measured in the legs of healthy subjects (4.40 ± 1.47, P < 0.001). The post-exercise/rest PCr and NAD+/NADH ratios were lower in the legs of patients with PAD (n = 3) when compared with the legs of healthy subjects (n = 6) (0.79 ± 0.06 vs 1.00 ± 0.07 (P = 0.004) and 1.15 ± 0.43 vs 2.08 ± 0.30 (P = 0.007), respectively). SMBF increased post-exercise to the greatest degree in the symptomatic legs of patients with PAD and post-exercise skeletal muscle mitochondrial function was abnormal in patients with PAD. These data suggest that the causes of symptoms and reduced exercise capacity from PAD are not limited to abnormal perfusion pressure in the legs. [Display omitted] The pathophysiology of symptoms and reduced exercise capacity from peripheral artery disease (PAD) remains unclear. Additionally, there is limited information on blood flow and skeletal muscle energetics after walking exercise in patients with claudication in comparison to healthy individuals. We prospectively enrolled 19 patients with claudication from PAD and 12 healthy subjects. All participants underwent rest and post-exercise perfusion imaging of the lower leg muscles via PET/CT. Participants exercised on a treadmill following the Gardner-Skinner protocol. Skeletal muscle blood flow (SMBF) was quantified in each leg at rest and immediately after exercise. Phosphocreatine (PCr) recovery and NAD /NADH concentrations were measured pre- and post-exercise by P magnetic resonance spectroscopy (MRS) in a subset of participants. Comparisons were made between the legs of healthy subjects and the asymptomatic and symptomatic legs of patients with PAD. SMBF increased post-exercise in all participants. Among patients with PAD, the post-exercise/rest SMBF ratio, was higher in the symptomatic (n = 25) than asymptomatic (n = 13) legs (8.03 ± 2.84 vs 6.03 ± 2.81, P = 0.046) and higher than the post-exercise/rest SMBF ratio measured in the legs of healthy subjects (4.40 ± 1.47, P < 0.001). The post-exercise/rest PCr and NAD /NADH ratios were lower in the legs of patients with PAD (n = 3) when compared with the legs of healthy subjects (n = 6) (0.79 ± 0.06 vs 1.00 ± 0.07 (P = 0.004) and 1.15 ± 0.43 vs 2.08 ± 0.30 (P = 0.007), respectively). SMBF increased post-exercise to the greatest degree in the symptomatic legs of patients with PAD and post-exercise skeletal muscle mitochondrial function was abnormal in patients with PAD. These data suggest that the causes of symptoms and reduced exercise capacity from PAD are not limited to abnormal perfusion pressure in the legs. |
ArticleNumber | 102143 |
Author | Gerhard-Herman, Marie D. Belkin, Michael Divakaran, Sanjay Di Carli, Marcelo F. Feinberg, Mark W. Lin, Alexander P. Park, Mi-Ae Martell, Laurel B. Barrett, Leanne Morgan, Victoria Yang, David Kijewski, Marie F. Creager, Mark A. Harms, Hendrik J. Merugumala, Sai K. Bonaca, Marc P. Robertson, Matthew Jarolim, Petr Perillo, Anna |
Author_xml | – sequence: 1 givenname: Sanjay orcidid: 0000-0003-0598-6502 surname: Divakaran fullname: Divakaran, Sanjay email: sdivakaran@bwh.harvard.edu organization: Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 2 givenname: Hendrik J. surname: Harms fullname: Harms, Hendrik J. organization: Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 3 givenname: Matthew surname: Robertson fullname: Robertson, Matthew organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 4 givenname: Sai K. surname: Merugumala fullname: Merugumala, Sai K. organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 5 givenname: Mi-Ae orcidid: 0000-0003-0806-129X surname: Park fullname: Park, Mi-Ae organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 6 givenname: Marie F. surname: Kijewski fullname: Kijewski, Marie F. organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 7 givenname: Laurel B. surname: Martell fullname: Martell, Laurel B. organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 8 givenname: Victoria surname: Morgan fullname: Morgan, Victoria organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 9 givenname: Leanne orcidid: 0000-0003-0667-8720 surname: Barrett fullname: Barrett, Leanne organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 10 givenname: Anna orcidid: 0009-0009-0083-2759 surname: Perillo fullname: Perillo, Anna organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 11 givenname: David surname: Yang fullname: Yang, David organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 12 givenname: Petr surname: Jarolim fullname: Jarolim, Petr organization: Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 13 givenname: Mark W. orcidid: 0000-0001-9523-3859 surname: Feinberg fullname: Feinberg, Mark W. organization: Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 14 givenname: Marie D. surname: Gerhard-Herman fullname: Gerhard-Herman, Marie D. organization: Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 15 givenname: Michael surname: Belkin fullname: Belkin, Michael organization: Department of Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 16 givenname: Alexander P. surname: Lin fullname: Lin, Alexander P. organization: Department of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA – sequence: 17 givenname: Mark A. orcidid: 0000-0001-9758-6447 surname: Creager fullname: Creager, Mark A. organization: Heart and Vascular Center, Dartmouth Hitchcock Medical Center, Lebanon, NH, USA – sequence: 18 givenname: Marc P. orcidid: 0000-0002-9860-3584 surname: Bonaca fullname: Bonaca, Marc P. organization: CPC Clinical Research, University of Colorado School of Medicine, Aurora, CO, USA – sequence: 19 givenname: Marcelo F. surname: Di Carli fullname: Di Carli, Marcelo F. organization: Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA |
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Keywords | Peripheral artery disease Claudication Skeletal muscle perfusion Microvascular disease Skeletal muscle metabolism |
Language | English |
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Snippet | The pathophysiology of symptoms and reduced exercise capacity from peripheral artery disease (PAD) remains unclear. Additionally, there is limited... The pathophysiology of symptoms and reduced exercise capacity from peripheral artery disease (PAD) remains unclear. Additionally, there is limited information... |
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SubjectTerms | Aged Claudication Exercise Test Female Humans Intermittent Claudication - diagnostic imaging Intermittent Claudication - physiopathology Lower Extremity - blood supply Magnetic Resonance Spectroscopy Male Microvascular disease Middle Aged Muscle, Skeletal - blood supply Muscle, Skeletal - diagnostic imaging Muscle, Skeletal - metabolism Muscle, Skeletal - physiopathology Peripheral Arterial Disease - diagnostic imaging Peripheral Arterial Disease - metabolism Peripheral Arterial Disease - physiopathology Peripheral artery disease Phosphocreatine - metabolism Positron Emission Tomography Computed Tomography Prospective Studies Skeletal muscle metabolism Skeletal muscle perfusion Walking - physiology |
Title | Post-walking exercise skeletal muscle perfusion and energetics in patients with symptomatic lower extremity peripheral artery disease |
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