1.Effect of urinary angiotensinogen and high-salt diet on blood pressure in patients with chronic kidney disease: results from the Korean Cohort Study for Outcome in Patients with Chronic Kidney Disease (KNOW-CKD)
Ha Yeon KIM ; Hong Sang CHOI ; Chang Seong KIM ; Eun Hui BAE ; Seong Kwon MA ; Su-Ah SUNG ; Seung Hyeok HAN ; Kook-Hwan OH ; Curie AHN ; Soo Wan KIM
The Korean Journal of Internal Medicine 2021;36(3):659-667
Background/Aims:
This study aimed to investigate whether urinary angiotensinogen (UAGT) excretion was associated with elevated blood pressure in patients with chronic kidney disease (CKD) and to evaluate the relationship among blood pressure, intra-renal renin-angiotensin system (RAS) activity, and dietary sodium in patients with CKD.
Methods:
Participants from the Korean Cohort Study for Outcome in Patients with Chronic Kidney Disease (KNOW-CKD) were included. Of the total cohort of 2,238 individuals with CKD, we included 1,955 participants who underwent complete 24-hour urinary sodium (24-hour UNa) analysis. They were categorized into three groups according to three tertiles of their 24-hour UNa, reflecting daily salt intake. To measure intra-renal RAS activity, the UAGT excretion was assayed with an enzyme-linked immunosorbent assay.
Results:
Elevated 24-hour UNa levels, logarithm of UAGT-to-creatinine ratio (UAGT/Cr), increased waist-to-hip ratio, and decreased estimated glomerular filtration rate were the risk factors for increased systolic blood pressure. Systolic blood pressure showed a positive correlation with 24-hour UNa levels and logarithm of UAGT/Cr.
Conclusions
UAGT and urinary sodium excretion are independent determinants of systolic blood pressure in patients with CKD. These findings suggest that increased systolic blood pressure in CKD patients is associated with both increased dietary sodium levels and intra-renal RAS activity. The risk of elevated systolic blood pressure in the 3rd tertile of both the UAGT/Cr and 24-hour UNa groups was about 2.3 times higher than that in the reference group.
2.Effect of urinary angiotensinogen and high-salt diet on blood pressure in patients with chronic kidney disease: results from the Korean Cohort Study for Outcome in Patients with Chronic Kidney Disease (KNOW-CKD)
Ha Yeon KIM ; Hong Sang CHOI ; Chang Seong KIM ; Eun Hui BAE ; Seong Kwon MA ; Su-Ah SUNG ; Seung Hyeok HAN ; Kook-Hwan OH ; Curie AHN ; Soo Wan KIM
The Korean Journal of Internal Medicine 2021;36(3):659-667
Background/Aims:
This study aimed to investigate whether urinary angiotensinogen (UAGT) excretion was associated with elevated blood pressure in patients with chronic kidney disease (CKD) and to evaluate the relationship among blood pressure, intra-renal renin-angiotensin system (RAS) activity, and dietary sodium in patients with CKD.
Methods:
Participants from the Korean Cohort Study for Outcome in Patients with Chronic Kidney Disease (KNOW-CKD) were included. Of the total cohort of 2,238 individuals with CKD, we included 1,955 participants who underwent complete 24-hour urinary sodium (24-hour UNa) analysis. They were categorized into three groups according to three tertiles of their 24-hour UNa, reflecting daily salt intake. To measure intra-renal RAS activity, the UAGT excretion was assayed with an enzyme-linked immunosorbent assay.
Results:
Elevated 24-hour UNa levels, logarithm of UAGT-to-creatinine ratio (UAGT/Cr), increased waist-to-hip ratio, and decreased estimated glomerular filtration rate were the risk factors for increased systolic blood pressure. Systolic blood pressure showed a positive correlation with 24-hour UNa levels and logarithm of UAGT/Cr.
Conclusions
UAGT and urinary sodium excretion are independent determinants of systolic blood pressure in patients with CKD. These findings suggest that increased systolic blood pressure in CKD patients is associated with both increased dietary sodium levels and intra-renal RAS activity. The risk of elevated systolic blood pressure in the 3rd tertile of both the UAGT/Cr and 24-hour UNa groups was about 2.3 times higher than that in the reference group.
3.Early surgical correction of microstomia followingStevens-Johnson syndrome
Sae Hwi KI ; Gang Yeon JO ; Sung Hwan MA ; Matthew Seung Suk CHOI
Archives of Craniofacial Surgery 2020;21(2):119-122
Stevens-Johnson syndrome (SJS) is a rare disease in which extensive toxic epidermolysis occursafter medication. Skin and mucous membranes are involved in about 90% of SJS cases, and webbingof mouth corners (microstomia) may occur when they are affected. Few reports have been issuedon microstomia in SJS, and no consensus has been reached regarding treatment methods,timings, or results. We encountered a case of microstomia following SJS after ofloxacin medicationin a 22-year-old woman treated by commissuroplasty using a lozenge-shaped excision. Wepresent an appropriate correction method and surgical timing for microstomia following SJS.
4.Osteotomy and iliac bone graft for the treatment of malunion caused by failed mandibular fracture reduction
Archives of Craniofacial Surgery 2020;21(6):384-386
This report describes osteotomy and iliac bone graft for malunion caused by failed mandibular fracture reduction. A 27-year-old man was referred 3 months after a motor vehicle accident. At another hospital, two operations had been performed for symphyseal fracture using two resorbable plates. Malocclusion was noted, and panoramic radiography and computed tomography revealed a misaligned dental arch, with a 9.37-mm gap between the central and the lateral incisor of the left mandible. A wafer was made from the patient’s dental model, and a maxillary arch bar was applied. Through a lower gingivolabial incision, osteotomy was performed between the malunited symphyseal fracture segments. Both segments were reduced to their original position using the wafer and fixed with titanium miniplates via intermaxillary fixation (IMF). The intersegmental gap was filled with cancellous bone from the iliac crest. The gingival defect was covered with a mucosal transposition flap from the gingivolabial sulcus. IMF and the wafer were maintained for 5 and 9 weeks, respectively. At postoperative week 13, the screws were removed from the mandible and satisfactory occlusion was noted. His mouth opening improved from 2.5 to 3 finger breadths (40 mm). This case demonstrates the need for sufficient IMF when using resorbable plates.
5.Unplanned change from double free flap to a chimeric anterolateral thigh flap in recurrent laryngeal cancer
Sae Hwi KI ; Sung Hwan MA ; Seung Hyun SIM ; Matthew Seung Suk CHOI
Archives of Craniofacial Surgery 2019;20(6):416-420
Reconstruction method choice in recurrent head and neck cancer depends on surgical history, radiation therapy dosage, conditions of recipient vessels, and general patient condition. Furthermore, when defects are multiple or three dimensional in nature, reconstruction and flap choice aimed at rebuilding the functional structure of the head and neck are difficult. We experienced successful reconstruction of recurrent laryngeal cancer requiring reconstruction of esophageal and tracheostomy stroma defects using a chimeric two-skin anterolateral thigh flap with a single pedicle.
Esophagus
;
Free Tissue Flaps
;
Head
;
Head and Neck Neoplasms
;
Humans
;
Laryngeal Neoplasms
;
Methods
;
Neck
;
Thigh
;
Tracheostomy
6.Panax Ginseng Induces Toxic Hepatitis and Acute Kidney Injury
Jeong Ho LEE ; Jung Hwan YOON ; Sung Sun KIM ; Seong Kwon MA ; Soo Wan KIM ; Eun Hui BAE
Chonnam Medical Journal 2017;53(2):168-169
No abstract available.
Acute Kidney Injury
;
Drug-Induced Liver Injury
;
Panax
7.Pyridoxine responsive sideroblastic anemia in a boy with mitral valve prolapse.
June Seung SUNG ; Ki Hwan KIM ; Dong Gyun HAN ; Mi Jeong KIM ; Young Kook CHO ; Hae Yul CHUNG ; Hee Jo BAEK ; Jae Sook MA ; Hoon KOOK ; Tai Ju HWANG
Korean Journal of Pediatrics 2006;49(11):1223-1226
Sideroblastic anemia is a rare, heterogeneous group of disorders characterized by hyperferremia, microcytic hypochromic anemia, and bone marrow erythroid hyperplasia with the presence of numerous ringed sideroblasts. We describe herewith the case of a rare coincidence of sideroblastic anemia and mitral valve prolapse with resultant regurgitation in a 2-year-old boy. In addition to the inherent propensity for the development of cardiac dysfunction in sideroblastic anemia due to transfusion-associated myocardial iron overload and chronic anemia, a coincidence of MVP will further increase the likelihood of the morbidity or mortality of th patient. in this patient. After response to pyridoxine, the patient remains in good condition with stable hemoglobin levels.
Anemia
;
Anemia, Hypochromic
;
Anemia, Sideroblastic*
;
Bone Marrow
;
Child, Preschool
;
Humans
;
Hyperplasia
;
Iron Overload
;
Male*
;
Mitral Valve Prolapse*
;
Mitral Valve*
;
Mortality
;
Pyridoxine*
8.Features of the Peripheral Nerve Injury in Patients with High Voltage Electrical Burn.
Yang Ki MINN ; Soo Jin CHO ; Ki Han KWON ; Hwan Suk PARK ; Young Hee SUNG ; Kyung Ho YU ; Hyeo Il MA
Journal of the Korean Neurological Association 2004;22(6):604-608
BACKGROUND: The peripheral nerve is known to be vulnerable to electrical injury. However, the character and mechanism of electrical injury to the peripheral nerve is not well established in clinical conditions. METHODS: We retrospectively reviewed the nerve conduction study (NCS) data of patients who had high voltage electrical injury in their upper extremities. RESULTS: Among 16 extremities studied, nine had abnormal NCS findings. Nine of 12 extremities, whose input/output were distal to wrist, showed abnormal NCS findings. In contrast, all four extremities, whose input/output points were their forearm, had normal NCS findings. In the patients who had abnormal NCS findings, the distal portion experienced more severe damage than the proximal portion. CONCLUSIONS: Input/output points are important factors in the electrical injury to the peripheral nerve. Joule heating seems to be a more important mechanism of electrical peripheral nerve injury.
Burns*
;
Extremities
;
Forearm
;
Heating
;
Hot Temperature
;
Humans
;
Neural Conduction
;
Peripheral Nerve Injuries*
;
Peripheral Nerves*
;
Retrospective Studies
;
Upper Extremity
;
Wrist
9.Cortical Dysplasia and Mesial Temporal Sclerosis in Temporal Lobe Epilepsy Pre-operative Clinical Feature and Surgical Outcome between Patients with Dual Pathology and Patients with Mesial Temporal Sclerosis.
Suk Yun KANG ; Joong Koo KANG ; Hyeo Il MA ; Kyu Hwan KWAK ; Jung Kyo LEE ; Sung Hye PARK ; Shin Kwang KHANG ; Sang Ahm LEE
Journal of the Korean Neurological Association 1999;17(6):810-815
BACKGROUND: Mesial temporal sclerosis (MTS) is a well-known cause of temporal lobe epilepsy. Coexistence with cortical dysplasia (CD) has been reported, but its role is not well recognized. This study aims to determine whether there is any difference about clinical feature and surgical outcome between patients with MTS and coexistent CD (group 1) and patients with isolated MTS (group 2). METHODS: Retrospectively, surgical series of 45 patients (male:22, female:23) diagnosed as temporal lobe epilepsy were reviewed. We excluded patients who had another pathology (e. g., tumor, vascular malformation) except MTS or CD. The pathology, case histories, interictal EEG, and surgical outcome were compared. RESULTS: There was a tendency for group 1 patients to have earlier seizure onset age (10.9+/-6.35 versus 14.5+/-6.03, p=0.06) There was no statistically significant difference in the history of febrile convulsions (68.4% versus 53.8%, p>0.16) No statistically significant difference between groups were also found in disease duration, the head trauma/mental retardation history, seizure frequency, interictal EEG, and surgical outcome. CONCLUSIONS: CD in MTS appears to have an influence on seizure onset. The relationships among CD, febrile convulsion, and mesial temporal sclerosis must be more investigated.
Age of Onset
;
Electroencephalography
;
Epilepsy, Temporal Lobe*
;
Head
;
Humans
;
Malformations of Cortical Development*
;
Pathology*
;
Retrospective Studies
;
Sclerosis*
;
Seizures
;
Seizures, Febrile
;
Temporal Lobe*
10.Cortical Dysplasia and Mesial Temporal Sclerosis in Temporal Lobe Epilepsy Pre-operative Clinical Feature and Surgical Outcome between Patients with Dual Pathology and Patients with Mesial Temporal Sclerosis.
Suk Yun KANG ; Joong Koo KANG ; Hyeo Il MA ; Kyu Hwan KWAK ; Jung Kyo LEE ; Sung Hye PARK ; Shin Kwang KHANG ; Sang Ahm LEE
Journal of the Korean Neurological Association 1999;17(6):810-815
BACKGROUND: Mesial temporal sclerosis (MTS) is a well-known cause of temporal lobe epilepsy. Coexistence with cortical dysplasia (CD) has been reported, but its role is not well recognized. This study aims to determine whether there is any difference about clinical feature and surgical outcome between patients with MTS and coexistent CD (group 1) and patients with isolated MTS (group 2). METHODS: Retrospectively, surgical series of 45 patients (male:22, female:23) diagnosed as temporal lobe epilepsy were reviewed. We excluded patients who had another pathology (e. g., tumor, vascular malformation) except MTS or CD. The pathology, case histories, interictal EEG, and surgical outcome were compared. RESULTS: There was a tendency for group 1 patients to have earlier seizure onset age (10.9+/-6.35 versus 14.5+/-6.03, p=0.06) There was no statistically significant difference in the history of febrile convulsions (68.4% versus 53.8%, p>0.16) No statistically significant difference between groups were also found in disease duration, the head trauma/mental retardation history, seizure frequency, interictal EEG, and surgical outcome. CONCLUSIONS: CD in MTS appears to have an influence on seizure onset. The relationships among CD, febrile convulsion, and mesial temporal sclerosis must be more investigated.
Age of Onset
;
Electroencephalography
;
Epilepsy, Temporal Lobe*
;
Head
;
Humans
;
Malformations of Cortical Development*
;
Pathology*
;
Retrospective Studies
;
Sclerosis*
;
Seizures
;
Seizures, Febrile
;
Temporal Lobe*

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