Metabolic Activity in Central Neural Structures of Patients With Myocardial Injury

Standard

Metabolic Activity in Central Neural Structures of Patients With Myocardial Injury. / Fiechter, Michael; Roggo, Andrea; Haider, Ahmed; Bengs, Susan; Burger, Irene A; Marędziak, Monika; Portmann, Angela; Treyer, Valerie; Becker, Anton S; Messerli, Michael; Mühlematter, Urs J; Kudura, Ken; von Felten, Elia; Benz, Dominik C; Fuchs, Tobias A; Gräni, Christoph; Pazhenkottil, Aju P; Buechel, Ronny R; Kaufmann, Philipp A; Gebhard, Catherine.

in: J AM HEART ASSOC, Jahrgang 8, Nr. 19, 10.2019, S. e013070.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Fiechter, M, Roggo, A, Haider, A, Bengs, S, Burger, IA, Marędziak, M, Portmann, A, Treyer, V, Becker, AS, Messerli, M, Mühlematter, UJ, Kudura, K, von Felten, E, Benz, DC, Fuchs, TA, Gräni, C, Pazhenkottil, AP, Buechel, RR, Kaufmann, PA & Gebhard, C 2019, 'Metabolic Activity in Central Neural Structures of Patients With Myocardial Injury', J AM HEART ASSOC, Jg. 8, Nr. 19, S. e013070. https://doi.org/10.1161/JAHA.119.013070

APA

Fiechter, M., Roggo, A., Haider, A., Bengs, S., Burger, I. A., Marędziak, M., Portmann, A., Treyer, V., Becker, A. S., Messerli, M., Mühlematter, U. J., Kudura, K., von Felten, E., Benz, D. C., Fuchs, T. A., Gräni, C., Pazhenkottil, A. P., Buechel, R. R., Kaufmann, P. A., & Gebhard, C. (2019). Metabolic Activity in Central Neural Structures of Patients With Myocardial Injury. J AM HEART ASSOC, 8(19), e013070. https://doi.org/10.1161/JAHA.119.013070

Vancouver

Fiechter M, Roggo A, Haider A, Bengs S, Burger IA, Marędziak M et al. Metabolic Activity in Central Neural Structures of Patients With Myocardial Injury. J AM HEART ASSOC. 2019 Okt;8(19):e013070. https://doi.org/10.1161/JAHA.119.013070

Bibtex

@article{3307ba61d0f14618bea1d3c51280b7d7,
title = "Metabolic Activity in Central Neural Structures of Patients With Myocardial Injury",
abstract = "Background Increasing evidence suggests a psychosomatic link between neural systems and the heart. In light of the growing burden of ischemic cardiovascular disease across the globe, a better understanding of heart-brain interactions and their implications for cardiovascular treatment strategies is needed. Thus, we sought to investigate the interaction between myocardial injury and metabolic alterations in central neural areas in patients with suspected or known coronary artery disease. Methods and Results The association between resting metabolic activity in distinct neural structures and cardiac function was analyzed in 302 patients (aged 66.8±10.2 years; 70.9% men) undergoing fluor-18-deoxyglucose positron emission tomography and 99mTc-tetrofosmin single-photon emission computed tomography myocardial perfusion imaging. There was evidence for reduction of callosal, caudate, and brainstem fluor-18-deoxyglucose uptake in patients with impaired left ventricular ejection fraction (<55% versus ≥55%: P=0.047, P=0.022, and P=0.013, respectively) and/or in the presence of myocardial ischemia (versus normal perfusion: P=0.010, P=0.013, and P=0.016, respectively). In a sex-stratified analysis, these differences were observed in men, but not in women. A first-order interaction term consisting of sex and impaired left ventricular ejection fraction or myocardial ischemia was identified as predictor of metabolic activity in these neural regions (left ventricular ejection fraction: P=0.015 for brainstem; myocardial ischemia: P=0.004, P=0.018, and P=0.003 for callosal, caudate, or brainstem metabolism, respectively). Conclusions Myocardial dysfunction and injury are associated with reduced resting metabolic activity of central neural structures, including the corpus callosum, the caudate nucleus, and the brainstem. These associations differ in women and men, suggesting sex differences in the pathophysiological interplay of the nervous and cardiovascular systems.",
author = "Michael Fiechter and Andrea Roggo and Ahmed Haider and Susan Bengs and Burger, {Irene A} and Monika Mar{\c e}dziak and Angela Portmann and Valerie Treyer and Becker, {Anton S} and Michael Messerli and M{\"u}hlematter, {Urs J} and Ken Kudura and {von Felten}, Elia and Benz, {Dominik C} and Fuchs, {Tobias A} and Christoph Gr{\"a}ni and Pazhenkottil, {Aju P} and Buechel, {Ronny R} and Kaufmann, {Philipp A} and Catherine Gebhard",
year = "2019",
month = oct,
doi = "10.1161/JAHA.119.013070",
language = "English",
volume = "8",
pages = "e013070",
journal = "J AM HEART ASSOC",
issn = "2047-9980",
publisher = "Wiley-Blackwell",
number = "19",

}

RIS

TY - JOUR

T1 - Metabolic Activity in Central Neural Structures of Patients With Myocardial Injury

AU - Fiechter, Michael

AU - Roggo, Andrea

AU - Haider, Ahmed

AU - Bengs, Susan

AU - Burger, Irene A

AU - Marędziak, Monika

AU - Portmann, Angela

AU - Treyer, Valerie

AU - Becker, Anton S

AU - Messerli, Michael

AU - Mühlematter, Urs J

AU - Kudura, Ken

AU - von Felten, Elia

AU - Benz, Dominik C

AU - Fuchs, Tobias A

AU - Gräni, Christoph

AU - Pazhenkottil, Aju P

AU - Buechel, Ronny R

AU - Kaufmann, Philipp A

AU - Gebhard, Catherine

PY - 2019/10

Y1 - 2019/10

N2 - Background Increasing evidence suggests a psychosomatic link between neural systems and the heart. In light of the growing burden of ischemic cardiovascular disease across the globe, a better understanding of heart-brain interactions and their implications for cardiovascular treatment strategies is needed. Thus, we sought to investigate the interaction between myocardial injury and metabolic alterations in central neural areas in patients with suspected or known coronary artery disease. Methods and Results The association between resting metabolic activity in distinct neural structures and cardiac function was analyzed in 302 patients (aged 66.8±10.2 years; 70.9% men) undergoing fluor-18-deoxyglucose positron emission tomography and 99mTc-tetrofosmin single-photon emission computed tomography myocardial perfusion imaging. There was evidence for reduction of callosal, caudate, and brainstem fluor-18-deoxyglucose uptake in patients with impaired left ventricular ejection fraction (<55% versus ≥55%: P=0.047, P=0.022, and P=0.013, respectively) and/or in the presence of myocardial ischemia (versus normal perfusion: P=0.010, P=0.013, and P=0.016, respectively). In a sex-stratified analysis, these differences were observed in men, but not in women. A first-order interaction term consisting of sex and impaired left ventricular ejection fraction or myocardial ischemia was identified as predictor of metabolic activity in these neural regions (left ventricular ejection fraction: P=0.015 for brainstem; myocardial ischemia: P=0.004, P=0.018, and P=0.003 for callosal, caudate, or brainstem metabolism, respectively). Conclusions Myocardial dysfunction and injury are associated with reduced resting metabolic activity of central neural structures, including the corpus callosum, the caudate nucleus, and the brainstem. These associations differ in women and men, suggesting sex differences in the pathophysiological interplay of the nervous and cardiovascular systems.

AB - Background Increasing evidence suggests a psychosomatic link between neural systems and the heart. In light of the growing burden of ischemic cardiovascular disease across the globe, a better understanding of heart-brain interactions and their implications for cardiovascular treatment strategies is needed. Thus, we sought to investigate the interaction between myocardial injury and metabolic alterations in central neural areas in patients with suspected or known coronary artery disease. Methods and Results The association between resting metabolic activity in distinct neural structures and cardiac function was analyzed in 302 patients (aged 66.8±10.2 years; 70.9% men) undergoing fluor-18-deoxyglucose positron emission tomography and 99mTc-tetrofosmin single-photon emission computed tomography myocardial perfusion imaging. There was evidence for reduction of callosal, caudate, and brainstem fluor-18-deoxyglucose uptake in patients with impaired left ventricular ejection fraction (<55% versus ≥55%: P=0.047, P=0.022, and P=0.013, respectively) and/or in the presence of myocardial ischemia (versus normal perfusion: P=0.010, P=0.013, and P=0.016, respectively). In a sex-stratified analysis, these differences were observed in men, but not in women. A first-order interaction term consisting of sex and impaired left ventricular ejection fraction or myocardial ischemia was identified as predictor of metabolic activity in these neural regions (left ventricular ejection fraction: P=0.015 for brainstem; myocardial ischemia: P=0.004, P=0.018, and P=0.003 for callosal, caudate, or brainstem metabolism, respectively). Conclusions Myocardial dysfunction and injury are associated with reduced resting metabolic activity of central neural structures, including the corpus callosum, the caudate nucleus, and the brainstem. These associations differ in women and men, suggesting sex differences in the pathophysiological interplay of the nervous and cardiovascular systems.

U2 - 10.1161/JAHA.119.013070

DO - 10.1161/JAHA.119.013070

M3 - SCORING: Journal article

C2 - 31566462

VL - 8

SP - e013070

JO - J AM HEART ASSOC

JF - J AM HEART ASSOC

SN - 2047-9980

IS - 19

ER -