Kyeong Min Son
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Kyeong Min Son has a total of 26 co-authors. Here are the top co-authors by number of shared publications:
- Chang Hoon Lee
Musculoskeletal and Immune Disease Research Institute, School of Medicine, Wonkwang University, 460 Iksandae-ro, Iksan 54538, Republic of Korea
3 shared publications - Chang-Nam Son
Division of Rheumatology, Department of Internal Medicine, Uijeongbu Eulji Medical Center, Eulji University School of Medicine, Uijeongbu 11749, Republic of Korea
3 shared publications - Hyo Jin Choi
Division of Rheumatology, Department of Internal Medicine, Gil Medical Center, Gachon University College of Medicine, Incheon, Korea
3 shared publications - Hyun-Ok Kim
Division of Rheumatology, Department of Internal Medicine, Gyeongsang National University College of Medicine, Jinju, Korea
3 shared publications - Joong Kyong Ahn
Division of Rheumatology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea
3 shared publications - Ki Won Moon
Division of Rheumatology, Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Korea
3 shared publications
Latest Publications
- Open Access
- 1 January 2026
- Published by XMLink in Journal of Korean Medical Science
- Vol. 41 (43)
Risk Factors for Gout Flares After Urate-Lowering Therapy: A Nationwide Prospective Cohort Study
Do H, et al. J Korean Med Sci. 2026 Nov;41:e296. https://doi.org/10.3346/jkms.2026.41.e296
- 1 January 2026
- Published by XMLink in Journal of Korean Medical Science
- Vol. 41 (43)
Open AccessRisk Factors for Gout Flares After Urate-Lowering Therapy: A Nationwide Prospective Cohort Study
Do H, et al. J Korean Med Sci. 2026 Nov;41:e296. https://doi.org/10.3346/jkms.2026.41.e296
- 1 December 2025
- Published by The Journal of Rheumatology in The Journal of Rheumatology
- Vol. 53 (3) , 322-328
Effectivity and Safety of Febuxostat in Reducing Serum Urate in Gout Patients With Chronic Kidney Disease: A Prospective Multicenter ULTRA Registry Study
Objective: Gout, an inflammatory arthritis caused by hyperuricemia, is highly prevalent with chronic kidney disease (CKD). We evaluated longitudinal changes in serum urate (SU) levels and febuxostat dosage according to renal function. Methods: Among 405 patients in the Urate-Lowering Therapy in Gout (ULTRA) registry between November 2021 and December 2023, 112 were analyzed after excluding those with < 1-year follow-up period, nonfebuxostat therapy, or missing data. SU levels and febuxostat doses were compared between the 2 groups at baseline, 6, and 12 months. Results: Baseline SU levels did not differ between the normal and CKD groups. After febuxostat therapy, mean (SD) SU levels were significantly lower in the CKD group than in the normal group (at 6 months: 4.45 [1.84] mg/dL vs 5.62 [1.62] mg/dL, P = 0.001; at 12 months: 4.81 [1.81] mg/dL vs 5.60 [1.94] mg/dL, P = 0.04). Meanwhile, the mean dosages of febuxostat were lower in CKD group than in the normal group (at 6 months: 40.61 [22.07] mg vs 47.54 [19.43] mg, P = 0.11; at 12 months: 40.59 [21.73] mg vs 48.49 [19.70] mg, P = 0.06), although these differences were not statistically significant. Additionally, the proportion of patients achieving SU < 6 mg/dL at 6 months was higher in the CKD group than in the normal group (91.2% vs 68.6%, P = 0.01). Conclusion: An individualized dosing strategy based on SU response, rather than renal function alone, may optimize treatment outcomes in these patients.
- 1 December 2025
- Published by The Journal of Rheumatology in The Journal of Rheumatology
- Vol. 53 (3) , 322-328
Effectivity and Safety of Febuxostat in Reducing Serum Urate in Gout Patients With Chronic Kidney Disease: A Prospective Multicenter ULTRA Registry Study
Objective: Gout, an inflammatory arthritis caused by hyperuricemia, is highly prevalent with chronic kidney disease (CKD). We evaluated longitudinal changes in serum urate (SU) levels and febuxostat dosage according to renal function. Methods: Among 405 patients in the Urate-Lowering Therapy in Gout (ULTRA) registry between November 2021 and December 2023, 112 were analyzed after excluding those with < 1-year follow-up period, nonfebuxostat therapy, or missing data. SU levels and febuxostat doses were compared between the 2 groups at baseline, 6, and 12 months. Results: Baseline SU levels did not differ between the normal and CKD groups. After febuxostat therapy, mean (SD) SU levels were significantly lower in the CKD group than in the normal group (at 6 months: 4.45 [1.84] mg/dL vs 5.62 [1.62] mg/dL, P = 0.001; at 12 months: 4.81 [1.81] mg/dL vs 5.60 [1.94] mg/dL, P = 0.04). Meanwhile, the mean dosages of febuxostat were lower in CKD group than in the normal group (at 6 months: 40.61 [22.07] mg vs 47.54 [19.43] mg, P = 0.11; at 12 months: 40.59 [21.73] mg vs 48.49 [19.70] mg, P = 0.06), although these differences were not statistically significant. Additionally, the proportion of patients achieving SU < 6 mg/dL at 6 months was higher in the CKD group than in the normal group (91.2% vs 68.6%, P = 0.01). Conclusion: An individualized dosing strategy based on SU response, rather than renal function alone, may optimize treatment outcomes in these patients.
- Open Access
- 22 November 2023
- Published by Springer Nature in Scientific Reports
- Vol. 13 (1) , 1-7
Factors for achieving target serum uric acid levels after initiating urate-lowering therapy in patients with gout: results from the ULTRA registry
Achieving target serum uric acid (SUA) levels is important in gout management. Guidelines recommend lowering SUA levels to < 6 mg/dL; however, many patients fail to reach this target, even with uric acid-lowering therapy (ULT). This study investigated clinical characteristics of target SUA achievers among Korean patients with gout. This study used data from the ULTRA registry, a nationwide inception cohort established in September 2021 that enrolls patients with gout who initiate ULT. Demographic, clinical, and laboratory data were collected at baseline; the 6-month follow-up. Patients were divided into two groups: target achievers (SUA level < 6 mg/dL at 6 months) and non-achievers. The mean participant (N = 117) age was 56.1 years, and 88.0% were male. At 6 months, 83 patients (70.9%) reached target SUA levels. Target achievers had better drug adherence (≥ 80%) to ULT (97.6% vs. 76.5%; p < 0.01) than non-achievers. Target non-achievers had a higher percentage of a family history of gout (32.4% vs. 10.8%; p < 0.01) and less antihypertensive agent use (38.2% vs. 59.0%; p = 0.03) than target achievers. Multivariate regression analysis revealed that good adherence to ULT, the absence of a family history of gout, and antihypertensive agent use were key factors associated with achieving target SUA levels at 6 months.
- 22 November 2023
- Published by Springer Nature in Scientific Reports
- Vol. 13 (1) , 1-7
Open AccessFactors for achieving target serum uric acid levels after initiating urate-lowering therapy in patients with gout: results from the ULTRA registry
Achieving target serum uric acid (SUA) levels is important in gout management. Guidelines recommend lowering SUA levels to < 6 mg/dL; however, many patients fail to reach this target, even with uric acid-lowering therapy (ULT). This study investigated clinical characteristics of target SUA achievers among Korean patients with gout. This study used data from the ULTRA registry, a nationwide inception cohort established in September 2021 that enrolls patients with gout who initiate ULT. Demographic, clinical, and laboratory data were collected at baseline; the 6-month follow-up. Patients were divided into two groups: target achievers (SUA level < 6 mg/dL at 6 months) and non-achievers. The mean participant (N = 117) age was 56.1 years, and 88.0% were male. At 6 months, 83 patients (70.9%) reached target SUA levels. Target achievers had better drug adherence (≥ 80%) to ULT (97.6% vs. 76.5%; p < 0.01) than non-achievers. Target non-achievers had a higher percentage of a family history of gout (32.4% vs. 10.8%; p < 0.01) and less antihypertensive agent use (38.2% vs. 59.0%; p = 0.03) than target achievers. Multivariate regression analysis revealed that good adherence to ULT, the absence of a family history of gout, and antihypertensive agent use were key factors associated with achieving target SUA levels at 6 months.
- Open Access
- 1 January 2010
- Published by Korean College of Rheumatology in The Journal of the Korean Rheumatism Association
- Vol. 17 (2) , 162-167
Adherence to Uric Acid Lowering Agent of Gouty Patients
Son KM, et al. J Korean Rheum Assoc. 2010 Jun;17(2):162-167. http://dx.doi.org/10.4078/jkra.2010.17.2.162
- 1 January 2010
- Published by Korean College of Rheumatology in The Journal of the Korean Rheumatism Association
- Vol. 17 (2) , 162-167
Open AccessAdherence to Uric Acid Lowering Agent of Gouty Patients
Son KM, et al. J Korean Rheum Assoc. 2010 Jun;17(2):162-167. http://dx.doi.org/10.4078/jkra.2010.17.2.162