Kyu-yong Ko

Dr. Kyu-yong Ko

Yonsei University, Seoul, Republic of Korea
orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2014 in EuroIntervention
Verified
Journal Article
Closed access
SWSUNGIL WOO
SUNGIL WOO
SPSang-Don Park
Sang-Don Park
DKDae-Hyeok Kim
Dae-Hyeok Kim
JKJun Kwan
Jun Kwan
SSSung-Hee Shin
Sung-Hee Shin
SKSoo-Hyeon Kim
Soo-Hyeon Kim
The Official Journal of EuroPCR and the European Association of Percutaneous Cardiovascular Interventions (EAPCI)

7 May 2022 in Cancers
Verified
Journal Article
Open access
PDF file
SLSeon-Hwa Lee
Seon-Hwa Lee
ICIksung Cho
Iksung Cho
SYSeng Chan You
Seng Chan You
MCMin-Jae Cha
Min-Jae Cha
JCJeesuk Chang
Jeesuk Chang
HKHyo Song Kim
Hyo Song Kim
Backgrounds: There are scarce data on whether immune checkpoint inhibitors (ICIs) increase the risk of cardiac dysfunction when used with cardiotoxic agents. Thus, we evaluated cardiac dysfunction in patients with sarcoma receiving doxorubicin with or without ICI using echocardiography and left ventricular global longitudinal strain (LVGLS). Methods: A total of 95 patients were included in this study. Echocardiography and LVGLS were evaluated at baseline and follow-up (at 3 and 6 months of chemotherapy) and compared with the doxorubicin (Dox; n = 73) and concomitant ICI with doxorubicin (Dox-ICI; n = 22) groups. Cancer therapy-related cardiac dysfunction (CTRCD) was defined as a left ventricular ejection fraction (LVEF) drop of >10% and LVEF of 10%, LVEF of ≥50%, and LVGLS relative reduction of >15% (probable CTRCD) at six months. Results: There were no significant differences in age, cumulative dose of doxorubicin, and cardiovascular risk factors between the two groups. At baseline, the LVEF was similar in the Dox and Dox-ICI groups (p = 0.493). In the Dox group, LVEF decreased to 59 ± 6% (Δ −7 ± 1.3%, p < 0.001) and LVGLS decreased from −17.3 ± 3.2% to −15.4 ± 3.2% (Δ −10.1 ± −1.9%, p < 0.001) at six months. In the Dox-ICI group, LVEF decreased to 55 ± 9% (Δ −9 ± 2.1%, p < 0.001), along with a significant decrease in LVGLS (from −18.6 ± 1.9% to −15.3 ± 3.6%, Δ −12.4 ± −2.4%, p < 0.001). Over a median follow-up of 192 days, there were no cases with clinical manifestations of fulminant myocarditis. In the Dox group, definite and probable CTRCD were observed in seven (10.1%) and five (7.4%) patients, respectively. In the Dox-ICI group, definite and probable CTRCD were observed in four (19%) and four (19%) patients, respectively. The total number of patients who developed CTRCD was significantly higher in the Dox-ICI group than in the Dox group (38.1% vs. 17.4%, p = 0.042). Serum troponin-T level was significantly higher in the Dox-ICI group than in the Dox group (53.3 vs. 27.5 pg/mL, p = 0.023). Conclusions: ICIs may increase the risk of CTRCD when used with cardiotoxic agents. CTRCD should be monitored in patients treated with ICIs by cardiac biomarkers and echocardiography, including LV-GLS.

3 September 2019 in Heart and Vessels
Verified
Journal Article
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JJJi-Hun Jang
Ji-Hun Jang
SSSung-Hee Shin
Sung-Hee Shin
YBYong Soo Beak
Yong Soo Beak
KKKyu-yong Ko
Kyu-yong Ko
SKSung Woo Kwon
Sung Woo Kwon
JKJun Kwan
Jun Kwan

1 January 2026 in International Journal of Heart Failure
Verified
Journal Article
Open access
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CLChan Joo Lee
Chan Joo Lee
HLHokyou Lee
Hokyou Lee
KKKyu-yong Ko
Kyu-yong Ko
MKMin Gyu Kong
Min Gyu Kong
MKMin Sun Kim
Min Sun Kim
Byung Su YooByung Su Yoo
Byung Su Yoo
Lee CJ, et al. Int J Heart Fail. 2026 Jan;8(1):58-73. https://doi.org/10.36628/ijhf.2026.0001

1 January 2025 in Yonsei Medical Journal
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Journal Article
Open access
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DKDong-Gil Kim
Dong-Gil Kim
SCSungsoo Cho
Sungsoo Cho
SPSeongjin Park
Seongjin Park
GKGi Rim Kim
Gi Rim Kim
KKKyu-yong Ko
Kyu-yong Ko
SCSung Woo Cho
Sung Woo Cho
Kim DG, et al. Yonsei Med J. 2025 Jan;66(1):1-8. https://doi.org/10.3349/ymj.2023.0410

9 July 2020 in Journal of Interventional Cardiology
Verified
Journal Article
Open access
PDF file
JJJi-Hun Jang
Ji-Hun Jang
MLMan-Jong Lee
Man-Jong Lee
KKKyu-yong Ko
Kyu-yong Ko
JPJin-Hee Park
Jin-Hee Park
YBYong-Soo Baek
Yong-Soo Baek
SPSang-Don Park
Sang-Don Park
Objectives. We aimed to identify mechanical and pharmacological revascularization strategies correlated with the index of microcirculatory resistance (IMR) in ST-elevation myocardial infarction (STEMI) patients. Background. Microvascular dysfunction (MVD) after STEMI is correlated with infarct size and poor long-term prognosis, and the IMR is a useful analytical method for the quantitative assessment of MVD. However, therapeutic strategies that can reliably reduce MVD remain uncertain. Methods. Patients with STEMI who underwent primary percutaneous coronary intervention (PCI) were enrolled. The IMR was measured with a pressure sensor/thermistor-tipped guidewire immediately after primary PCI. High IMR was defined as values ≥66th percentile of IMR in enrolled patients (IMR > 30.9 IU). Results. A total of 160 STEMI patients were analyzed (high IMR = 54 patients). Clinical factors for Killip class P=0.006, delayed hospitalization from symptom onset P=0.004, peak troponin-I level P=0.042, and multivessel disease P=0.003 were associated with high IMR. Achieving final thrombolysis in myocardial infarction myocardial perfusion grade 3 tended to be associated with low IMR P=0.119, whereas the presence of distal embolization was significantly associated with high IMR P=0.034. In terms of therapeutic strategies that involved adjusting clinical and angiographic factors associated with IMR, preloading of third-generation P2Y12 inhibitors correlated with reducing IMR value (β = −10.30, P<0.001). Mechanical therapeutic strategies including stent diameter/length, preballoon dilatation, direct stenting, and thrombectomy were not associated with low IMR value (all P>0.05), and postballoon dilatation was associated with high IMR (β = 8.30, P=0.020). Conclusions. In our study, mechanical strategies were suboptimal in achieving myocardial salvage. Preloading of third-generation P2Y12 inhibitors revealed decreased IMR value, indicative of MVD prevention.