JAYOUNG KIM

Dr. JAYOUNG KIM

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Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

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

Representative Publications

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1 November 2019 in Annals of Laboratory Medicine
Verified
Journal Article
Open access
PDF file
DPDong Chul Park
Dong Chul Park
Si Hyun KimSi Hyun Kim
Si Hyun Kim
DYDongeun Yong
Dongeun Yong
ISIn Bum Suh
In Bum Suh
YKYoung Ah Kim
Young Ah Kim
JSJeong Hwan Shin
Jeong Hwan Shin
Park DC, et al. Ann Lab Med. 2019 Nov;39(6):537-544. https://doi.org/10.3343/alm.2019.39.6.537

Hyeyun KimHyeyun Kim
Hyeyun Kim
JKJAYOUNG KIM
JAYOUNG KIM
HJHyo jin Ju
Hyo jin Ju
BJBong Jin Jang
Bong Jin Jang
TWTae Kyu Wang
Tae Kyu Wang
YKYeong In Kim
Yeong In Kim
Female hormone changes during menopause can affect the autonomic nervous system, circadian rhythm, and secretion of cortisol/melatonin, resulting in a vulnerability to insomnia. In this light, therapy has been gaining attention as a way to reduce stress hormones by stabilizing the autonomic nervous system. Thus, this study aims to objectively and scientifically analyze the impact of forest therapy in postmenopausal insomnia patients. The forest therapy program lasted 6 days, wherein 35 postmenopausal women performed activities such as trekking, leg massages, stretches, and bathing in warm and cold water. They also underwent serologic tests, participated in polysomnography (PSG), and answered sleep questionnaires before and after the program. Further, a statistical analysis compared the results. Serologic tests showed a significant reduction of cortisol from 10.2 ± 3.79 to 7.75 ± 2.81, while PSGs showed how sleep efficiency increased to 89.3 ± 4.3% (p < 0.01), and how waking after sleep onset reduced to 47.4 ± 22.3 min (p < 0.01). The total sleep time also increased to 428.5 min and sleep latency was 11.1 ± 11.0 min. Despite its limitations, forest therapy could be a good alternative to nonpharmacological treatment for mitigating insomnia in postmenopausal women.

17 November 2020 in Advanced Healthcare Materials
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Journal Article
Closed access
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YSYujie Shi
Yujie Shi
ZZZongmin Zhao
Zongmin Zhao
KPKevin Peng
Kevin Peng
YGYongsheng Gao
Yongsheng Gao
DWDebra Wu
Debra Wu
SMSamir Mitragotri
Samir Mitragotri

1 January 2019 in Yonsei Medical Journal
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Journal Article
Open access
JCJi Seon Choi
Ji Seon Choi
IPIkchun Park
Ikchun Park
SLSoo Jung Lee
Soo Jung Lee
JHJu Hyojin
Ju Hyojin
HLHyeyoung Lee
Hyeyoung Lee
JKJAYOUNG KIM
JAYOUNG KIM
Bone markers can be useful for the diagnosis and treatment of skeletal diseases in children and adolescents. Owing to high skeletal growth velocity and rapid bone turnover, children and adolescents have higher bone marker levels than adults. Thus, a valid age- and sex-specific reference should be established for pediatric populations living in similar environments. We aimed to assess the associations of procollagen type I N-terminal propeptide (P1NP) and osteocalcin with age and sex in a group of healthy Korean children and adolescents. The participants (290 boys and 290 girls, age range 0-18 years) were Korean outpatients. Serum P1NP and osteocalcin levels were measured in control materials and patient samples by electrochemiluminescence immunoassay using an automated Cobas e411 analyzer. Significant age-dependent variations in bone marker levels were observed in both sexes (p<0.001). The highest P1NP levels were observed during the first year of life; thereafter, levels decreased until puberty. There was no postnatal peak for osteocalcin; however, its levels remained higher than the adult reference range throughout childhood. Significant differences were observed between boys and girls (p<0.05), especially between the ages of 12 and 17 years. Cobas e411 results for P1NP showed satisfactory precision and linearity. We established reference data for P1NP and osteocalcin levels in healthy Korean children and adolescents, as the first and only study of these parameters in pre-adulthood in Korea. Cobas e411-quantified bone markers may be useful for determining bone metabolism indices.

3 September 2019 in Mycobiology
Verified
Journal Article
Open access
JPJi-Hyun Park
Ji-Hyun Park
JOJunsang Oh
Junsang Oh
Hyunkyu SangHyunkyu Sang
Hyunkyu Sang
BSBhushan Shrestha
Bhushan Shrestha
HLHyeyoung Lee
Hyeyoung Lee
GSGi-Ho Sung
Gi-Ho Sung
Invasive fungal infections caused by Cyberlindnera fabianii have recently increased. However, biochemical kits such as API 20 C AUX and Vitek-2C have misidentified this species as other Candida spp. such as C. pelliculosa or C. utilis due to no information of Cy. fabianii in yeast database. During our 2016–2017 surveys, eleven isolates of Cy. fabianii were obtained in International St. Mary’s Hospital in Korea. Here, we describe its morphological and molecular characteristics and tested its antifungal susceptibility against nine antifungal agents. The sequences of the ITS region and the D1/D2 region of LSU revealed 100% identity with the sequences of Cy. fabianii. In comparison with the results from MALDI-TOF mass spectrometry, we found that Cy. fabianii can be distinguished from other species. In antifungal susceptibility test, voriconazole and echinocandins exhibited good antifungal activities against the majority of Cy. fabianii isolates despite the absence of standard criteria.

1 March 2022 in Annals of Laboratory Medicine
Verified
Journal Article
Open access
PDF file
Si Hyun KimSi Hyun Kim
Si Hyun Kim
GSGyung-Hye Sung
Gyung-Hye Sung
EPEun Hee Park
Eun Hee Park
IHIn Yeong Hwang
In Yeong Hwang
GKGyu Ri Kim
Gyu Ri Kim
JSJeong Hwan Shin
Jeong Hwan Shin
Si Hyun Kim, Ph.D., Gyung-Hye Sung, Ph.D., Eun Hee Park, Ph.D., In Yeong Hwang, Ph.D., Gyu Ri Kim, Ph.D., Sae Am Song, M.D., Hae Kyung Lee, M.D., Young Uh, M.D., Young Ah Kim, M.D., Seok Hoon Jeong, M.D., Jong Hee Shin, M.D., Kyeong Seob Shin, M.D., Jaehyeon Lee, M.D., Joseph Jeong, M.D., Young Ree Kim, M.D., Dongeun Yong, M.D., Miae Lee, M.D., Yu Kyung Kim, M.D., Nam Hee Ryoo, M.D., Seungok Lee, M.D., Jayoung Kim, M.D., Sunjoo Kim, M.D., Hyun Soo Kim, M.D., and Jeong Hwan Shin, M.D.. Ann Lab Med 2022;42:268-73. https://doi.org/10.3343/alm.2022.42.2.268