• 한국임상약학회지
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• 제16권1호
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• pp.14-22
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• 2006

Purpose: To determine the short (1 year of transplant) and long-term (1-5 years of transplantation) risk factors affecting the graft and patient survival in kidney transplantation recipients. Methods: Records of 149 patients who received kidney transplantation in 1996 from Asan Medical Center were followed for 5 years retrospectively. Results: All patients initiated triple immunosuppressive therapy with cyclosporine, prednisone and azathioprine. One, two, three, four, five year patient and graft survival rates were 98.7%, 98.0%, 98.0%, 97.3%, 97.3%, and 96.6%, 95.2%, 94.6%, 92.5%, 91.8%, respectively. There were 30 cases of acute rejection (AR) and 6 cases of chronic rejection (CR) within $2.1{\pm}3.2$ months and $42.1{\pm}13.2$ months of transplantation, respectively. The risk factors for AR were donor's age older than 30 years (p=0.02) and cardiovascular disease (p=0.05). The risk factors for CR were AR (p=0.0169) and episode of complications (p=0.0330). Increasing period of dialysis (p=0.0473), episodes of AR (p<0.0001) and complication (p=0.0317) were significant factors for graft loss. Seven grafts were lost from noncompliance during 1-5 year period. The most com- mon cause of the graft loss for both periods was the graft rejection. The graft survival rate was significantly lower in patients with than without rejection episodes (77.4% vs. 90.0%, p=0.002). Conclusions: Survival rate of the graft with rejection was significantly lower. The risk factors affecting AR were donor's age older than 30years and CVD. AR and episode of complications within 1year were the risk factors for CR and graft loss.

• Childhood Kidney Diseases
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• 제3권2호
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• pp.130-144
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• 1999

목적 : Cyclosporine A(CsA)의 장기적인 치료에서 CsA의 신독성에 의하여 나타나게 되는 만성적인 신조직의 변화는 구심성 소동맥의 수축으로 인한 신혈류의 감소에서 시작되어, 신세뇨관의 위축과 간질조직의 섬유화를 포함하는 비특이적인 간질성 신염과 비교적 특징적이라 할 수 있는 사구체 주위 소동맥의 변화로 나타나게 된다. 본 연구에서는 원발성 및 이차성 신증후군의 CsA치료에서 치료기간 및 원발성 질환에 따른 조직학적인 신독성의 빈도 및 임상적인 신독성과의 관계를 알아보고 최적의 치료기간을 결정하고자 하였다. 방법 : 1986년부터 1997년까지 본원 소아과에서 신장조직검사로 확진된 신증후군 환아 중 스테로이드 저항성, 빈발 재발형 혹은 스테로이드 의존성으로 인하여 CsA로 치료받았던 102례(미세변화신증후군 58례, 국소성분절성 사구체신염 10례, 막성사구체신염 10례, 자반성신염 15례, IgA신병증 9례)를 대상으로 하였다. CsA를 미세변화신 증후군은 1년간 24례, 1.5년간 12례 2년간 22례에서 투여하였고, 국소성 분절성 사구체 경화증은 1년간 2례, 1.5년간 2례, 2년간 6례에서, 막성사구체신염은 1년간 8례, 2년간 2례에서 투여하였다. 자반성신염 과 IgA신병증은 모든 례에서 1년간 사용하였다. 전체 대상 환아에서 치료전과 치료 종료후 1개월 째 신장조직검사를 시행하여 신독성 여부를 조사하였다. 결과 : 전체대상 환아에서 신증후군의 완전관해율은 86%였다(미세변화증후군 96%, 막성사구체신염 90%, 국소성분절성사구체경화증 60%, 자반성신염 80%, IgA 신병증 55%). 스테로이드 반응성의 미세변화신증후군 및 국소성분절성사구체경화증 환아에서 CsA치료후 6개월간의 재발의 빈도는 각각 $0.5{\pm}0.7$회, $0.8{\pm}0.3$회로 치료전 6개월간(각각 $1.8{\pm}0.8$회, $2.0{\pm}0.7$회)에 비하여 의미있게 감소하였다(P<0.0001). 전체 102례의 신증후군 환아중 71례(69.6%)에서 치료전후에 조직학적인 변화를 보이지 않았고 24례(23.5%)에서 간질성 신염을 보였으며 7례(6.8%)에서 혈관변화를 보였다. 미세변화신증후군 환아에서 CsA치료후 관찰된 간질성 신염의 빈도는 1년, 1.5년, 2년 치료군이 각각 16.6%, 33.3%, 27.2%였고, 혈관변화의 빈도는 1년, 1.5년, 2년 치료군이 각각 0%, 16.6%, 9%였다. 임상적인 신독성의 소견은 한례에서도 보이지 않았으며 1년이상 사용군에서 1년이하의 사용군에 비하여 통계적으로 유의하게 조직학적 신독성의 빈도가 증가함을 보였다(P=0.03). 발병연령, 성별, 원인질환에 따른 조직학적인 신독성의 빈도의 의미있는 차이를 보이지 않았다. 결론 : 소아의 원발성 및 이차성 신증후군의 CsA치료에서 치료기간이 의미 있는 만성조직학적 신독성의 위험인자로 나타났으며, 신독성의 위험을 최소화 할 수 있는 적절한 CsA 치료기간은 1년 이하가 바람직 하며, CsA에 의한 신장의 조직학적인 변화는 임상적인 신기능의 감소와 무관하게 나타날 수 있으므로, 조직학적인 신독성을 찾아내는뎨 있어서 신장조직검사의 중요성이 반드시 고려되어야 할 것으로 생각되었다.

• Journal of Acupuncture Research
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• 제17권1호
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• pp.67-74
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• 2000

Hominis Placenta has been used as a medicinal stuff for a long time in Oriental Medicine. And further, aqua-acupuncture solution of Hominis Placenta has produced in South Korea recently. Bibliographical study was carried on to investigate the nature of Hominis Placenta and possible indications by aqua-acupuncture as well. The nature of Hominis Placenta is warm and its taste sweet-salty. It is non-poisonous. It has correspondence to the meridians of lung, liver and kidney. Hominis Placenta is mainly effective on recuperation of infirmity and the disease related to infirmity. Aqua-acupuncture solution of Hominis Placenta can be applied to the disease as chronic hepatitis, liver cirrhosis, asthma, pulmonary tuberculosis, sterility, insufficient lactation, degenerative change, neurasthenia and cerebrovascular disease.

• Childhood Kidney Diseases
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• 제1권2호
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• pp.183-188
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• 1997

Familial juvenile hyperuricemic nephropathy is an autosomal dominant disease characterized by progressive renal disease and hyperuricemia or gout, affecting young people of either sex equally. There are two biochemical markers of this disorder. The first is hyperuricemia disproportionate to the degree of renal dysfunction; the second is a grossly reduced clearance of uric acid relative to creatinine, dispropotionate to age, sex and degree of renal failure. We experienced 2 family members with hyperuricemia. One family member, a 13-year-old girl who had suffered from tophaceous gout and chronic renal failure. Her younger brother also had hyperuricemia and moderately reduced renal function. Their urinary excretion fractions of uric acid($FE_{uric\;acid}$) were reduced and renal biopsy specimens showed interstitial fibrosis with tubular atrophy and interstitial urate crystal deposition. We have treated these two patients with allopurinol but we have done renal transplantation because she progressed to end stage renal disease at 16 year old age.

• Childhood Kidney Diseases
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• 제25권2호
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• pp.92-111
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• 2021

Purpose: Nephrotic syndrome (NS) is the most common form of glomerulopathy in children. Most pediatric patients respond to glucocorticosteroid treatment (steroid-sensitive NS, SSNS), while approximately 10-15% will remain unresponsive or later become steroid-resistant. There has been a long-standing effort to find biomarkers that may predict steroid responsiveness. Methods: We systematically reviewed current studies which investigated clinically relevant biomarkers for predicting steroid responsiveness in pediatric NS. We performed a PubMed and EMBASE search to identify eligible articles. We collected data on urinary markers, blood/serum markers (including cellular phenotypes and mRNA expression), genotypes and HLA allele frequency. Results: A total of 659 articles were identified following electronic and manual searches. After reviewing the titles, abstracts, and full texts, 72 eligible articles were finally included. Vitamin D-binding protein (VDBP) seemed to be significantly elevated in SRNS than in SSNS, in both serum and urine specimen, although further validation is required. Conclusions: The present paper narratively illustrates current understandings of potential biomarkers that may help predict steroid responsiveness. Further investigation and collaboration involving a larger number of patients are necessary.

• 한국식생활문화학회지
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• 제37권3호
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• pp.248-255
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• 2022

Spinach (Spinacia oleracea L.), a green leafy vegetable, is well known as a functional food due to its biological activities. Vascular calcification is associated with several disease conditions including atherosclerosis, diabetes, and chronic kidney disease (CKD), and is known to raise the risk of cardiovascular diseases related morbidity and mortality. However, there are no previous studies that have investigated the effects of fermented spinach exract (FSE) against aortic and its underlying mechanisms. Therefore, this study investigated the effects and action of possible mechanisms of FSE on inorganic phosphate (PI)-induced vascular calcification in ex vivo mouse aortic rings. PI increased vascular calcification through calcium deposition in ex vivo aortic rings. FSE inhibited calcium accumulation and osteogenic key marker, runt-related transcription factor 2 (Runx2), and bone Morphogenetic Protein 2 (BMP-2) protein expression in ex vivo aortic rings. And, FSE inhibited PI-induced extracellular signal-regulated kinase (ERK) and p38 phosphorylation in ex vivo aortic rings. These results show that FSE can prevent vascular calcification which may be a crucial way for the prevention and treatment of vascular disease association with vascular calcification.

• 멤브레인
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• 제34권2호
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• pp.105-113
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• 2024

만성 콩팥병은 많은 사람들이 말기병으로 진단받고 있다. 이 질병은 혈액이 막과 투석기에 의해 세척되는 과정인 혈액투석에 의해 치료된다. 혈액투석을 위한 막은 혈액에서 불순물인 요소를 선택적으로 제거하는 역할을 하기 때문에 이 과정은 중요한 첫 단계이다. 다양한 종류의 고분자로 구성된 막이 사용되지만, 낮은 선택도와 혈액적합성과 같은 다양한 단점을 가지고 있다. 이를 해결하기 위해 여러 논문에서 서로 다른 고분자의 혼합물을 사용하여 기공의 크기를 변화시키고 혈액적합성을 높이며 선택성을 높이는 연구를 진행하였다. 그동안 보고된 논문들을 통해 혼합막이 더 큰 장점을 가지고 있음을 알 수 있었다.

• 한국임상약학회지
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• 제30권3호
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• pp.169-176
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• 2020

Background: Most meta-analyses of risk factors for severe or critical outcomes in patients with COVID-19 only included studies conducted in China and this causes difficulties in generalization. Therefore, this study aimed to systematically evaluate the risk factors in patients with COVID-19 from various countries. Methods: PubMed, Embase, and Web of Science were searched for studies published on the mortality risk in patients with COVID-19 from January 1 to May 7, 2020. Pooled estimates were calculated as odds ratio (OR) with 95% confidence interval (CI) using the random-effects model. Results: We analyzed data from seven studies involving 26,542 patients in total in this systematic review and meta-analysis. Among the patients, 2,337 deaths were recorded (8.8%). Elderly patients and males showed significantly higher mortality rates than young patients and females; the OR values were 3.6 (95% CI 2.5-5.1) and 1.2 (95% CI 1.0-1.3), respectively. Among comorbidities, hypertension (OR 2.3, 95% CI 1.1-4.6), diabetes (OR 2.2, 95% CI 1.2-3.9), cardiovascular disease (OR 3.1, 95% CI 1.5-6.3), chronic obstructive pulmonary disease (OR 4.4, 95% CI 1.7-11.5), and chronic kidney disease (OR 4.2, 95% CI 2.0-8.6) were significantly associated with increased mortalities. Conclusion: This meta-analysis, involving a huge global sample, employed a systematic method for synthesizing quantitative results of studies on the risk factors for mortality in patients with COVID-19. It is helpful for clinicians to identify patients with poor prognosis and improve the allocation of health resources to patients who need them most.

• International Journal of Computer Science & Network Security
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• 제23권12호
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• pp.101-106
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• 2023

Chronic illnesses are among the most common serious problems affecting human health. Early diagnosis of chronic diseases can assist to avoid or mitigate their consequences, potentially decreasing mortality rates. Using machine learning algorithms to identify risk factors is an exciting strategy. The issue with existing feature selection approaches is that each method provides a distinct set of properties that affect model correctness, and present methods cannot perform well on huge multidimensional datasets. We would like to introduce a novel model that contains a feature selection approach that selects optimal characteristics from big multidimensional data sets to provide reliable predictions of chronic illnesses without sacrificing data uniqueness.[1] To ensure the success of our proposed model, we employed balanced classes by employing hybrid balanced class sampling methods on the original dataset, as well as methods for data pre-processing and data transformation, to provide credible data for the training model. We ran and assessed our model on datasets with binary and multivalued classifications. We have used multiple datasets (Parkinson, arrythmia, breast cancer, kidney, diabetes). Suitable features are selected by using the Hybrid feature model consists of Lassocv, decision tree, random forest, gradient boosting,Adaboost, stochastic gradient descent and done voting of attributes which are common output from these methods.Accuracy of original dataset before applying framework is recorded and evaluated against reduced data set of attributes accuracy. The results are shown separately to provide comparisons. Based on the result analysis, we can conclude that our proposed model produced the highest accuracy on multi valued class datasets than on binary class attributes.[1]

• Childhood Kidney Diseases
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• 제20권2호
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• pp.83-87
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• 2016

Congenital chloride diarrhea (CLD) is a rare autosomal recessive disease that is difficult to diagnose. CLD requires early treatment to correct electrolyte imbalance and alkalosis and to prevent severe dehydration. Renal injury is clearly associated with defective electrolyte balance induced by CLD, particularly during the first months or years of life. A 7-year-old boy was diagnosed with CLD following detection of a homozygous mutation (c.2063-1G>T) in SLC26A3 at 6 months of age. During treatment with electrolyte supplements, mild proteinuria was detected at 8 months of age, and is still present. Renal biopsy showed the presence of focal renal dysplasia, with metaplastic cartilage and mononuclear cell infiltration, calcification, and fibrosis in the interstitium. Up to two-thirds of the glomeruli exhibited global obsolescence, mostly aggregated in the dysplastic area. In nondysplastic areas, the glomeruli were markedly increased in size and severely hypercellular, with increased mesangial matrix, and displayed segmental sclerosis. The marked glomerular hypertrophy with focal segmental glomerulosclerosis suggested a compensatory reaction to the severe nephron loss or glomerular obsolescence associated with renal dysplasia, with superimposed by CLD aggravating the tubulointerstitial damage.