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258


Mechanisms of Myocardial Infarction in Women Without Angiographically Obstructive Coronary Artery Disease

Reynolds HR; Srichai MB; Iqbal SN; Slater JN; Mancini GB; Feit F; Pena-Sing I; Axel L; Attubato MJ; Yatskar L; Kalhorn RT; Wood DA; Lobach IV; Hochman JS
BACKGROUND: . Unique identifier: NCT00798122
PMCID:3619391
PMID: 21900087
ISSN: 1524-4539
CID: 137093

ESC working group position paper on myocardial infarction with non-obstructive coronary arteries

Agewall, Stefan; Beltrame, John F; Reynolds, Harmony R; Niessner, Alexander; Rosano, Giuseppe; Caforio, Alida L P; De Caterina, Raffaele; Zimarino, Marco; Roffi, Marco; Kjeldsen, Keld; Atar, Dan; Kaski, Juan C; Sechtem, Udo; Tornvall, Per
PMID: 28158518
ISSN: 1522-9645
CID: 2435942

Autonomic Findings in Takotsubo Cardiomyopathy

Norcliffe-Kaufmann, Lucy; Kaufmann, Horacio; Martinez, Jose; Katz, Stuart D; Tully, Lisa; Reynolds, Harmony R
Takotsubo cardiomyopathy (TC) often occurs after emotional or physical stress. Norepinephrine levels are unusually high in the acute phase, suggesting a hyperadrenergic mechanism. Comparatively little is known about parasympathetic function in patients with TC. We sought to characterize autonomic function at rest and in response to physical and emotional stimuli in 10 women with a confirmed history of TC and 10 age-matched healthy women. Sympathetic and parasympathetic activity was assessed at rest and during baroreflex stimulation (Valsalva maneuver and tilt testing), cognitive stimulation (Stroop test), and emotional stimulation (event recall, patients). Ambulatory blood pressure monitoring and measurement of brachial artery flow-mediated vasodilation were also performed. TC women (tested an average of 37 months after the event) had excessive pressor responses to cognitive stress (Stroop test: p <0.001 vs baseline and p = 0.03 vs controls) and emotional arousal (recall of TC event: p = 0.03 vs baseline). Pressor responses to hemodynamic stimuli were also amplified (Valsalva overshoot: p <0.05) and prolonged (duration: p <0.01) in the TC women compared with controls. Plasma catecholamine levels did not differ between TC women and controls. Indexes of parasympathetic (vagal) modulation of heart rate induced by respiration and cardiovagal baroreflex gain were significantly decreased in the TC women versus controls. In conclusion, even long after the initial episode, women with previous episode of TC have excessive sympathetic responsiveness and reduced parasympathetic modulation of heart rate. Impaired baroreflex control may therefore play a role in TC.
PMID: 26743349
ISSN: 1879-1913
CID: 1901192

Sex Differences in Revascularization, Treatment Goals, and Outcomes of Patients With Chronic Coronary Disease: Insights From the ISCHEMIA Trial

Reynolds, Harmony R; Cyr, Derek D; Merz, C Noel Bairey; Shaw, Leslee J; Chaitman, Bernard R; Boden, William E; Alexander, Karen P; Rosenberg, Yves D; Bangalore, Sripal; Stone, Gregg W; Held, Claes; Spertus, John; Goetschalckx, Kaatje; Bockeria, Olga; Newman, Jonathan D; Berger, Jeffrey S; Elghamaz, Ahmed; Lopes, Renato D; Min, James K; Berman, Daniel S; Picard, Michael H; Kwong, Raymond Y; Harrington, Robert A; Thomas, Boban; O'Brien, Sean M; Maron, David J; Hochman, Judith S; ,
BACKGROUND:Women with chronic coronary disease are generally older than men and have more comorbidities but less atherosclerosis. We explored sex differences in revascularization, guideline-directed medical therapy, and outcomes among patients with chronic coronary disease with ischemia on stress testing, with and without invasive management. METHODS AND RESULTS/RESULTS:=0.49), with no significant sex-by-treatment-group interactions. CONCLUSIONS:Women had less extensive coronary artery disease and, therefore, lower revascularization rates in the invasive group. Despite lower risk factor goal attainment, women with chronic coronary disease experienced similar risk-adjusted outcomes to men in the ISCHEMIA trial. REGISTRATION/BACKGROUND:URL: http://wwwclinicaltrials.gov. Unique identifier: NCT01471522.
PMCID:10944079
PMID: 38410945
ISSN: 2047-9980
CID: 5645612

Coronary Microvascular Dysfunction Is Associated With a Proinflammatory Circulating Transcriptome in Patients With Nonobstructive Coronary Arteries

Smilowitz, Nathaniel R; Schlamp, Florencia; Hausvater, Anaïs; Joa, Amanda; Serrano-Gomez, Claudia; Farid, Ayman; Hochman, Judith S; Barrett, Tessa; Reynolds, Harmony R; Berger, Jeffrey S
PMID: 38299358
ISSN: 1524-4636
CID: 5627252

Global Longitudinal Strain as Predictor of Inducible Ischemia in No Obstructive Coronary Artery Disease in the CIAO-ISCHEMIA Study

Davis, Esther F; Crousillat, Daniela R; Peteiro, Jesus; Lopez-Sendon, Jose; Senior, Roxy; Shapiro, Michael D; Pellikka, Patricia A; Lyubarova, Radmila; Alfakih, Khaled; Abdul-Nour, Khaled; Anthopolos, Rebecca; Xu, Yifan; Kunichoff, Dennis M; Fleg, Jerome L; Spertus, John A; Hochman, Judith; Maron, David; Picard, Michael H; Reynolds, Harmony R; ,
BACKGROUND:Global longitudinal strain (GLS) is a sensitive marker for identifying subclinical myocardial dysfunction in obstructive coronary artery disease (CAD). Little is known about the relationship between GLS and ischemia in patients with myocardial ischemia and no obstructive CAD (INOCA). OBJECTIVES/OBJECTIVE:To investigate the relationship between resting GLS and ischemia on stress echocardiography (SE) in patients with INOCA. METHODS:Left ventricular GLS was calculated offline on resting SE images at enrollment (n = 144) and 1-year follow-up (n = 120) in the CIAO-ISCHEMIA (Changes in Ischemia and Angina over One year in International Study of Comparative Health Effectiveness with Medical and Invasive Approaches trial screen failures with no obstructive CAD on computed tomography [CT] angiography) study, which enrolled participants with moderate or severe ischemia by local SE interpretation (≥3 segments with new or worsening wall motion abnormality and no obstructive (<50% stenosis) on coronary computed tomography angiography. RESULTS:Global longitudinal strain values were normal in 83.3% at enrollment and 94.2% at follow-up. Global longitudinal strain values were not associated with a positive SE at enrollment (GLS = -21.5% positive SE vs GLS = -19.9% negative SE, P = .443) or follow-up (GLS = -23.2% positive SE vs GLS = -23.1% negative SE, P = .859). Significant change in GLS was not associated with positive SE in follow-up (P = .401). Regional strain was not associated with colocalizing ischemia at enrollment or follow-up. Changes in GLS and number of ischemic segments from enrollment to follow-up showed a modest but not clinically meaningful correlation (β = 0.41; 95% CI, 0.16, 0.67; P = .002). CONCLUSIONS:In this cohort of INOCA patients, resting GLS values were largely normal and did not associate with the presence, severity, or location of stress-induced ischemia. These findings may suggest the absence of subclinical myocardial dysfunction detectable by echocardiographic strain analysis at rest in INOCA.
PMID: 37722490
ISSN: 1097-6795
CID: 5603252

Reallocating time between device-measured 24-hour activities and cardiovascular risk in Asian American immigrant women: An isotemporal substitution model

Park, Chorong; Larsen, Britta; Kwon, Simona C; Xia, Yuhe; LaNoue, Marianna; Dickson, Victoria V; Reynolds, Harmony R; Spruill, Tanya M
The 24-hour day consists of physical activity (PA), sedentary behavior, and sleep, and changing the time spent on one activity affects the others. Little is known about the impact of such changes on cardiovascular risk, particularly in Asian American immigrant (AAI) women, who not only have a higher cardiovascular risk but also place greater cultural value on family and domestic responsibilities compared to other racial/ethnic groups. The purpose of this study was to evaluate the effects of reallocating 30 minutes of each 24-hour activity component for another on BMI, waist circumference, and blood pressure in AAI women. Seventy-five AAI women completed 7 days of hip and wrist actigraphy monitoring and were included in the analysis (age = 61.5±8.0 years, BMI = 25.5±3.6 kg/m2, waist circumference = 85.9±10.2 cm). Sleep was identified from wrist actigraphy data, and moderate-to-vigorous PA (MVPA), light PA, and sedentary behavior identified from hip actigraphy data. On average, the women spent 0.5 hours in MVPA, 6.2 hours in light PA, 10 hours in sedentary activities, and 5.3 hours sleeping within a 24-hour day. According to the isotemporal substitution models, replacing 30 minutes of sedentary behavior with MVPA reduced BMI by 1.4 kg/m2 and waist circumference by 4.0 cm. Replacing that same sedentary time with sleep reduced BMI by 0.5 kg/m2 and waist circumference by 1.4 cm. Replacing 30 minutes of light PA with MVPA decreased BMI by 1.6 kg/m2 and waist circumference by 4.3 cm. Replacing 30 minutes of light PA with sleep also reduced BMI by 0.8 kg/m2 and waist circumference by 1.7 cm. However, none of the behavioral substitutions affected blood pressure. Considering AAI women's short sleep duration, replacing their sedentary time with sleep might be a feasible strategy to reduce their BMI and waist circumference.
PMCID:10781047
PMID: 38198483
ISSN: 1932-6203
CID: 5628652

Reallocating time between device-measured 24-hour activities and cardiovascular risk in Asian American immigrant women: An isotemporal substitution model

Park, Chorong; Larsen, Britta; Kwon, Simona C.; Xia, Yuhe; LaNoue, Marianna; Dickson, Victoria V.; Reynolds, Harmony R.; Spruill, Tanya M.
ISI:001153638300021
ISSN: 1932-6203
CID: 5636322

Author Correction: Optical coherence tomography in coronary atherosclerosis assessment and intervention

Araki, Makoto; Park, Seung-Jung; Dauerman, Harold L; Uemura, Shiro; Kim, Jung-Sun; Di Mario, Carlo; Johnson, Thomas W; Guagliumi, Giulio; Kastrati, Adnan; Joner, Michael; Holm, Niels Ramsing; Alfonso, Fernando; Wijns, William; Adriaenssens, Tom; Nef, Holger; Rioufol, Gilles; Amabile, Nicolas; Souteyrand, Geraud; Meneveau, Nicolas; Gerbaud, Edouard; Opolski, Maksymilian P; Gonzalo, Nieves; Tearney, Guillermo J; Bouma, Brett; Aguirre, Aaron D; Mintz, Gary S; Stone, Gregg W; Bourantas, Christos V; Räber, Lorenz; Gili, Sebastiano; Mizuno, Kyoichi; Kimura, Shigeki; Shinke, Toshiro; Hong, Myeong-Ki; Jang, Yangsoo; Cho, Jin Man; Yan, Bryan P; Porto, Italo; Niccoli, Giampaolo; Montone, Rocco A; Thondapu, Vikas; Papafaklis, Michail I; Michalis, Lampros K; Reynolds, Harmony; Saw, Jacqueline; Libby, Peter; Weisz, Giora; Iannaccone, Mario; Gori, Tommaso; Toutouzas, Konstantinos; Yonetsu, Taishi; Minami, Yoshiyasu; Takano, Masamichi; Raffel, O Christopher; Kurihara, Osamu; Soeda, Tsunenari; Sugiyama, Tomoyo; Kim, Hyung Oh; Lee, Tetsumin; Higuma, Takumi; Nakajima, Akihiro; Yamamoto, Erika; Bryniarski, Krzysztof L; Di Vito, Luca; Vergallo, Rocco; Fracassi, Francesco; Russo, Michele; Seegers, Lena M; McNulty, Iris; Park, Sangjoon; Feldman, Marc; Escaned, Javier; Prati, Francesco; Arbustini, Eloisa; Pinto, Fausto J; Waksman, Ron; Garcia-Garcia, Hector M; Maehara, Akiko; Ali, Ziad; Finn, Aloke V; Virmani, Renu; Kini, Annapoorna S; Daemen, Joost; Kume, Teruyoshi; Hibi, Kiyoshi; Tanaka, Atsushi; Akasaka, Takashi; Kubo, Takashi; Yasuda, Satoshi; Croce, Kevin; Granada, Juan F; Lerman, Amir; Prasad, Abhiram; Regar, Evelyn; Saito, Yoshihiko; Sankardas, Mullasari Ajit; Subban, Vijayakumar; Weissman, Neil J; Chen, Yundai; Yu, Bo; Nicholls, Stephen J; Barlis, Peter; West, Nick E J; Arbab-Zadeh, Armin; Ye, Jong Chul; Dijkstra, Jouke; Lee, Hang; Narula, Jagat; Crea, Filippo; Nakamura, Sunao; Kakuta, Tsunekazu; Fujimoto, James; Fuster, Valentin; Jang, Ik-Kyung
PMID: 38110566
ISSN: 1759-5010
CID: 5611732

Biomarkers and cardiovascular events in patients with stable coronary disease in the ISCHEMIA Trials

Newman, Jonathan D; Anthopolos, Rebecca; Ruggles, Kelly V; Cornwell, Macintosh; Reynolds, Harmony R; Bangalore, Sripal; Mavromatis, Kreton; Held, Claes; Wallentin, Lars; Kullo, Iftikar J; McManus, Bruce; Newby, L Kristin K; Rosenberg, Yves; Hochman, Judith S; Maron, David J; Berger, Jeffrey S; ,
IMPORTANCE:Biomarkers may improve prediction of cardiovascular events for patients with stable coronary artery disease (CAD), but their importance in addition to clinical tests of inducible ischemia and CAD severity is unknown. OBJECTIVES:To evaluate the prognostic value of multiple biomarkers in stable outpatients with obstructive CAD and moderate or severe inducible ischemia. DESIGN AND SETTING:The ISCHEMIA and ISCHEMIA CKD trials randomized 5,956 participants with CAD to invasive or conservative management from July 2012 to January 2018; 1,064 participated in the biorepository. MAIN OUTCOME MEASURES:Primary outcome was cardiovascular death, myocardial infarction (MI), or hospitalization for unstable angina, heart failure, or resuscitated cardiac arrest. Secondary outcome was cardiovascular death or MI. Improvements in prediction were assessed by cause-specific hazard ratios (HR) and area under the receiver operating characteristics curve (AUC) for an interquartile increase in each biomarker, controlling for other biomarkers, in a base clinical model of risk factors, left ventricular ejection fraction (LVEF) and ischemia severity. Secondary analyses were performed among patients in whom core-lab confirmed severity of CAD was ascertained by computed cardiac tomographic angiography (CCTA). EXPOSURES:Baseline levels of interleukin-6 (IL-6), high sensitivity troponin T (hsTnT), growth differentiation factor 15 (GDF-15), N-terminal pro-B-type natriuretic peptide (NT-proBNP), lipoprotein a (Lp[a]), high sensitivity C-reactive protein (hsCRP), Cystatin C, soluble CD 40 ligand (sCD40L), myeloperoxidase (MPO), and matrix metalloproteinase 3 (MMP3). RESULTS:Among 757 biorepository participants, median (IQR) follow-up was 3 (2-5) years, age was 67 (61-72) years, and 144 (19%) were female; 508 had severity of CAD by CCTA available. In an adjusted multimarker model with hsTnT, GDF-15, NT-proBNP and sCD40L, the adjusted HR for the primary outcome per interquartile increase in each biomarker was 1.58 (95% CI 1.22, 2.205), 1.60 (95% CI 1.16, 2.20), 1.61 (95% 1.22, 2.14), and 1.46 (95% 1.12, 1.90), respectively. The adjusted multimarker model also improved prediction compared with the clinical model, increasing the AUC from 0.710 to 0.792 (P < .01) and 0.714 to 0.783 (P < .01) for the primary and secondary outcomes, respectively. Similar findings were observed after adjusting for core-lab confirmed atherosclerosis severity. CONCLUSIONS AND RELEVANCE:Among ISCHEMIA biorepository participants, biomarkers of myocyte injury/distension, inflammation, and platelet activity improved cardiovascular event prediction in addition to risk factors, LVEF, and assessments of ischemia and atherosclerosis severity. These biomarkers may improve risk stratification for patients with stable CAD.
PMID: 37604357
ISSN: 1097-6744
CID: 5598422