Soo Kyoung Kim

Prof. Soo Kyoung Kim

Department of Internal Medicine, Gyeongsang National University Hospital 90 Chilam-dong

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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19 September 2012 in Cardiovascular Diabetology
Verified
Journal Article
Open access
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CLChung Eun Lee
Chung Eun Lee
CYChin-Ok Yi
Chin-Ok Yi
BJByeong Tak Jeon
Byeong Tak Jeon
HSHyun Joo Shin
Hyun Joo Shin
SKSoo Kyoung Kim
Soo Kyoung Kim
GRGu Seob Roh
Gu Seob Roh
Background: Hyperglycemia leads to cardiac oxidative stress and an imbalance in glucose homeostasis. Diabetic cardiomyopathy is characterised by cardiac hypertrophy and fibrosis. However, the underlying mechanisms of diabetic cardiomyopathy are not fully understood. This study aimed to investigate the effects of alpha-lipoic acid (ALA) on cardiac energy metabolism, antioxidant effect, and fibrosis in the hearts of Otsuka Long-Evans Tokushima fatty (OLETF) rats. Methods: Animals were separated into non-diabetic Long-Evans Tokushima Otsuka (LETO) rats and diabetes-prone OLETF rats with or without ALA (200 mg/kg/day) administration for 16 weeks. Diabetic cardiomyopathy was assessed by staining with Sirius Red. The effect of ALA on AMPK signalling, antioxidant enzymes, and fibrosis-related genes in the heart of OLETF rats were performed by Western blot analysis or immunohistochemistry. Results: Western blot analysis showed that cardiac adenosine monophosphate-activated kinase (AMPK) signalling was lower in OLETF rats than in LETO rats, and that ALA treatment increased the signalling in OLETF rats. Furthermore, the low antioxidant activity in OLETF rats was increased by ALA treatment. In addition to increased Sirius red staining of collagen deposits, transforming growth factor-β1 (TGF-β1) and connective tissue growth factor (CTGF) were expressed at higher levels in OLETF rat hearts than in LETO rat hearts, and the levels of these factors were decreased by ALA. Conclusions: ALA enhances AMPK signalling, antioxidant, and antifibrogenic effect. Theses findings suggest that ALA may have beneficial effects in the treatment of diabetic cardiomyopathy.

1 February 2018 in Thyroid®
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Journal Article
Closed access
KKKyung Hee Kim
Kyung Hee Kim
MGMee Ock Gu
Mee Ock Gu
JJJunghwa Jung
Junghwa Jung
JHJong Ryeal Hahm
Jong Ryeal Hahm
SKSoo Kyoung Kim
Soo Kyoung Kim
SWSeung Hoon Woo
Seung Hoon Woo
Background: The objective of this study was to determine the effect of a home-based exercise program on fatigue, anxiety, quality of life, and immune function of thyroid cancer patients taking thyroid hormone replacement after thyroidectomy. Method: This quasi-experimental study with a non-equivalent control group included 43 outpatients taking thyroid hormone replacement after thyroidectomy (22 in experimental group and 21 in control group). After education about the home-based exercise program, subjects in the experimental group underwent 12 weeks of aerobic, resistance, and flexibility exercise. Analysis was conducted between the two groups. Results: Patients in the experimental group were significantly less fatigued or anxious (both p < 0.01). They professed significantly improved quality of life (p < 0.05) compared to those in the control group. Natural killer cell activity was significantly higher in the exercise group compared to that in the control group (p < 0.05). Conclusion: A home-based exercise program is effective in reducing fatigue and anxiety, improving quality of life, and increasing immune function in patients taking thyroid hormone replacement after thyroidectomy. Therefore, such home-based exercise program can be used as an intervention for patients who are taking thyroid hormone replacement after thyroidectomy.

21 October 2021 in Antioxidants
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HKHeeyoung Kang
Heeyoung Kang
HSHyun Joo Shin
Hyun Joo Shin
HAHyeong Seok An
Hyeong Seok An
ZJZhen Jin
Zhen Jin
JLJong Youl Lee
Jong Youl Lee
GRGu Seob Roh
Gu Seob Roh
Lipocalin-2 (LCN2) is an inflammatory protein with diverse functions in the brain. Although many studies have investigated the mechanism of LCN2 in brain injuries, the effect of LCN2 on amyloid-toxicity-related memory deficits in a mouse model of Alzheimer’s disease (AD) has been less studied. We investigated the role of LCN2 in human AD patients using a mouse model of AD. We created an AD mouse model by injecting amyloid-beta oligomer (AβO) into the hippocampus. In this model, animals exhibited impaired learning and memory. We found LCN2 upregulation in the human brain frontal lobe, as well as a positive correlation between white matter ischemic changes and serum LCN2. We also found increased astrocytic LCN2, microglia activation, iron accumulation, and blood–brain barrier disruption in AβO-treated hippocampi. These findings suggest that LCN2 is involved in a variety of amyloid toxicity mechanisms, especially neuroinflammation and oxidative stress.

1 January 2021 in Journal of Clinical Neurology
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Journal Article
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PCPil-Wook Chung
Pil-Wook Chung
JPJeong-Wook Park
Jeong-Wook Park
JSJong-Hee Sohn
Jong-Hee Sohn
MLMi Ji Lee
Mi Ji Lee
BKByung-Kun Kim
Byung-Kun Kim
SCSoo-Jin Cho
Soo-Jin Cho
Chung PW, et al. J Clin Neurol. 2021 Apr;17(2):229-235. https://doi.org/10.3988/jcn.2021.17.2.229

15 April 2020 in The Journal of Headache and Pain
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Journal Article
Open access
PDF file
SKSoo Kyoung Kim
Soo Kyoung Kim
CCCatherine D. Chong
Catherine D. Chong
GDGina Dumkrieger
Gina Dumkrieger
KRKatherine Ross
Katherine Ross
VBVisar Berisha
Visar Berisha
TSTodd J. Schwedt
Todd J. Schwedt
Background: Close associations between insomnia with other clinical factors have been identified in migraine, but there have been few studies investigating associations between insomnia and clinical factors in patients with persistent post-traumatic headache (PPTH). The study objective was to contrast the severity of insomnia symptoms in PPTH, migraine, and healthy controls, and to identify factors associated with insomnia in patients with PPTH vs. migraine. Methods: In this cross-sectional cohort study, 57 individuals with PPTH attributed to mild traumatic brain injury, 39 with migraine, and 39 healthy controls were included. Participants completed a detailed headache characteristics questionnaire, the Migraine Disability Assessment Scale (MIDAS), Insomnia Severity Index (ISI), Hyperacusis Questionnaire (HQ), Allodynia Symptom Checklist, Photosensitivity Assessment Questionnaire, Beck Depression Inventory (BDI), State-Trait Anxiety Inventory, Post-Traumatic Stress Disorder (PTSD) checklist, Ray Auditory Verbal Learning Test, and the Trail Making Test A and B to assess headache characteristics, disability, insomnia symptoms, sensory hypersensitivities, and neuropsychological factors. Fisher’s test and one-way ANOVA or Tukey’s Honest Significant Difference were used to assess group differences of categorical and continuous data. Stepwise linear regression analyses were conducted to identify clinical variables associated with insomnia symptoms. Results: Those with PPTH had significantly higher ISI scores (16.7 ± 6.6) compared to migraine patients (11.3 ± 6.4) and healthy controls (4.1 ± 4.8) (p < 0.001). For those with PPTH, insomnia severity was most strongly correlated with the BDI (Spearman’s rho (ρ) = 0.634, p < 0.01), followed by Trait Anxiety (ρ = 0.522, p < 0.01), PTSD (ρ = 0.505, p < 0.01), HQ (ρ = 0.469, p < 0.01), State Anxiety (ρ = 0.437, p < 0.01), and MIDAS scores (ρ = 0.364, p < 0.01). According to linear regression models, BDI, headache intensity, and hyperacusis scores were significantly positively associated with insomnia severity in those with PPTH, while only delayed memory recall was negatively associated with insomnia severity in those with migraine. Conclusions: Insomnia symptoms were more severe in those with PPTH compared to migraine and healthy control cohorts. Depression, headache intensity, and hyperacusis were associated with insomnia in individuals with PPTH. Future studies should determine the bidirectional impact of treating insomnia and its associated symptoms.

28 August 2015 in PLOS ONE
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Journal Article
Open access
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SKSungsu Kim
Sungsu Kim
JJJaehoon Jung
Jaehoon Jung
JJJung Hwa Jung
Jung Hwa Jung
SKSoo Kyoung Kim
Soo Kyoung Kim
RKRock-Bum Kim
Rock-Bum Kim
JHJong Ryeal Hahm
Jong Ryeal Hahm
Longitudinal studies on bone mass decline for healthy women are sparse. We performed a retrospective longitudinal study to evaluate the factor associated with bone mass changes at the lumbar spine in healthy Korean pre- and perimenopausal women over the age of 40. We examined the relation of blood tests including thyroid function tests at baseline and follow-up to the annual percentage changes in average BMD of L2-L4 (A%ΔLSBMD). Four hundred and forty-three subjects without diseases or medications pertaining to bone metabolism were analyzed. The mean A%ΔLSBMD in these subjects was -0.45%/year. Though a significant correlation was observed between the A%ΔLSBMD and age, serum thyroid-stimulating hormone (TSH) level, total cholesterol (TC) level, low-density lipoprotein cholesterol (LDL-C) level, and estimated glomerular filtration rate (eGFR) at baseline and follow-up, there was a weak correlation between A%ΔLSBMD and these variables. From multiple linear regression analyses, the percent body fat, age, serum TSH level, serum uric acid level, and the menopause at follow-up were showed to have a significant association with the A%ΔLSBMD. Unlike age, percent body fat, and menopause at follow-up, which had a negative association with the A%ΔLSBMD, serum TSH level and serum uric acid level, had a positive association with the A%ΔLSBMD. The results from our study showed that the notable risk factors of BMD loss at the lumbar spine in population of our study were advancing age, menopause, higher percent body fat, lower normal TSH, and lower serum uric acid levels.