1.A Study on Thyroid Function among Male Workers Occupationally Exposed to Inorganic Lead.
Hyeong Su KIM ; Yun Cheol PARK ; Jae Wook CHOI ; Woo Whan RHO ; Dae Seong KIM ; Jong Tae PARK
Korean Journal of Occupational and Environmental Medicine 1999;11(2):153-160
This study was performed to evaluate the relationship between biological markers of lead exposure and thyroid functions among male workers occupationally exposed to inorganic lead. 30 male workers exposed to inorganic lead at smelting and battery factories were investigated, and 30 male control workers who were not exposed to inorganic lead occupationally were chosen for this study. The data were obtained using direct interview and assessment of biological markers of lead exposure and thyroid indices. As biological markers for lead exposure, blood ZPP. blood lead, urine lead and hemoglobin were measured. As thyroid indices. TSH and FT4were determined. The results of the study were summarized as follows 1. Levels of ZPP, blood lead, and urine lead were significantly higher in lead-exposed group than in nonexposed control group(p<0.01 all). Hemoglobin level was significantly lower in lead-exposed group than in nonexposed group(p<0.01). 2. Study subjects had normal values of TSH and FT4 But TSH level was insignificantly lower in lead-exposed group than in nonexposed control group(p=0.11) and FT4 level was significantly lower in lead-exposed group than in nonexposed group(p<0.01). 3. As the result of simple regression analysis in lead-exposed group. FT4 level was negatively correlated with the amount of smoke, blood ZPP, and blood lead(p < 0.05 all). 4. In lead-exposed group, FT4 was used as a independent variable and age, the amount of smoke, blood ZPP, and blood lead were entered as a dependent variables in the model. As the result of multiple regression analysis with stepwise selection method, the amount of smoke and blood ZPP were negative predictors of FT4(p=0. 04, p=0.09, respectively). In conclusion, levels of TSH and FT4were lower in lead-exposed group than in nonexposed control group. In lead-exposed group, FT4 level was negatively correlated with amount of smoke, blood ZPP, and blood lead in simple regression analysis. To clarify this relation, further research between lead exposure and thyroid function may be required for worker with long-term lead exposure or high lead exposure.
Biological Markers
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Humans
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Male*
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Occupations*
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Osmeriformes
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Reference Values
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Smoke
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Thyroid Gland*
2.Clinical features and prognostic factors in Korean patients hospitalized for coronary artery disease (Catholic Heart Care Network Study).
Jin Man CHO ; Chong Jin KIM ; Woo Seung SHIN ; Eun Ju CHO ; Chul Soo PARK ; Pum Joon KIM ; Jong Min LEE ; Sang Hyun IHM ; Hyou Young RHIM ; Kiyuk CHANG ; Keon Woong MOON ; Yong Ju KIM ; Hae Ok JUNG ; Hee Yeol KIM ; Ji Won PARK ; Seung Won JIN ; Hui Kyung JEON ; Yong Seog OH ; Ki Dong YOO ; Doo Soo JEON ; Sang Hong BAEK ; Gil Whan LEE ; Ho Joong YOUN ; Man Young LEE ; Wook Sung CHUNG ; Jun Chul PARK ; Ki Bae SEUNG ; Tai Ho RHO ; Chul Min KIM ; In Soo PARK ; Jang Seong CHAE ; Jae Hyung KIM ; Kyu Bo CHOI ; Soon Jo HONG
Korean Journal of Medicine 2007;73(2):142-150
BACKGROUND: Coronary artery disease (CAD) has recently become one of the major causes of mortality and morbidity in Korea. However, not much epidemiologic and demographic data has yet been reported. The purpose of this study was to investigate the clinical features as well as the prognostic factors of patients with CAD. METHODS: We prospectively enrolled 1,665 consecutive patients with CAD who had been admitted to the Catholic University Hospitals from December 1999 to April 2003. RESULTS: Acute myocardial infarction (AMI) was the most common cause of admission (n=715, 42.9%). Dyslipidemia, hypertension and smoking were the most common risk factors. More than 70% of the patients who underwent percutaneous coronary intervention (PCI) received stent implantation. A total of 965 (612 males) patients were followed at least for 6 months (the mean follow-up duration was 23.8+/-12.2 months). The incidence rates of major adverse cardiac events (MACE: cardiac death, acute myocardial infarction, target vessel revascularization) and cardiac death were 15.1% (n=146) and 2.2% (n=21), respectively. There was no difference in overall survival between the patients treated with medical therapy and those treated with PCI. By Cox regression analysis, the independent prognostic factors for MACE were PCI (95% CI: 1.75-4.85; p<0.01) and multivessel disease (95% CI: 1.03-2.04; p<0.05), and the independent prognostic factors for cardiac death were medical therapy (95% CI: 1.08-14.41; p<0.05) and old age (95% CI: 1.13-16.13; p<0.05). CONCLUSIONS: There was no difference in overall survival between the patients treated with medical therapy and those treated with PCI. However, PCI was superior to medical therapy for preventing death of the patients with acute coronary syndrome.
Acute Coronary Syndrome
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Coronary Artery Disease*
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Coronary Disease
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Coronary Vessels*
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Death
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Dyslipidemias
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Follow-Up Studies
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Heart*
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Hospitals, University
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Humans
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Hypertension
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Incidence
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Korea
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Mortality
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Myocardial Infarction
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Percutaneous Coronary Intervention
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Prognosis
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Prospective Studies
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Risk Factors
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Smoke
;
Smoking
;
Stents
3.Korean multicenter clinical trial of simvastatin ( KS-1 study ).
Hyun Ho SHIN ; Kwon Bae KIM ; Jung Chaee KANG ; Min Soo SON ; Jae Hyung KIM ; Jong Seong KIM ; Seung Yun CHO ; Yung Woo SHIN ; Hyo Soo KIM ; In Ho CHAE ; Young Bae PARK ; Sung Choon CHOE ; Jung Don SEO ; Jong Hwa BAE ; Young Moo RHO ; Won Ro LEE ; Shung Chull CHAE ; Kwon Sam KIM ; Jung Chun AHN ; Cheol Ho KIM ; Jeong Euy PARK ; Cheol Whan LEE ; Jin Won JEONG ; Kyung Hoon CHOE ; Gil Ja SHIN ; Kun Joo RHEE ; Jae Ki KO ; Son Pyo HONG ; Un Ho RYOO ; Eun Seok JEON ; Dong Woon KIM ; Chong Yun RIM
Korean Journal of Medicine 1999;57(5):906-915
The aim of this study was to investigate the efficacy of simvastatin to improved lipid profiles in hypercholesterolemic Korean patients. METHODS: From 25 hospitals in Korea, 478 hypercholesterolemic patients were enrolled from November 1996 to April 1998. The inclusion criteria was hypercholesterolemia over 240 mg/dl after diet therapy for 1 month or hypercholesterolemia over 220 mg/dl in patients with definite evidence of ischemic heart disease. Simvastatin 10mg was started and doubled up to 40mg if total cholesterol level remained higher than 200 mg/dl at monthly check. Of 478 subjects, 344 patients in whom study protocol was not violated were analyzed. RESULTS: Male to female ratio was 27:73 and 47% of the subjects were in 6th decade. Hypertension, coronary artery disease, and diabetes mellitus were present in 30, 10, and 4% of the subjects. Baseline lipid profile (mean of total cholesterol-LDL-HDL-triglyceride mg/dl) was 274-185-52-188. The dose of simvastatin for 3 months was 10/10/10mg in 61% of subjects, 10/20/20mg in 21%, 10/10/20mg in 7%, and 10/20/40mg in 12%. The change of total cholesterol level(before-4wk-8wk-12wk-withdrawal 4wk) was 274-209- 205-198-250, and the maximal reduction rate was 27%. The change of LDL-cholesterol was 185-123-116-110-159, with maximal reduction rate 39%. The change of HDL-cholesterol was 52-54-56-55-54, with maximal increase rate 9%. The change of tryglyceride was 188-161- 164-162-189, with maximal reduction rate 15%. The value before/after treatment of ApoA1, ApoB, and Lp(a) was 129/129, 138/83, and 9.3/10.7, respectively. The level of LDL-cholesterol at the end of treatment was below 100mg/dl in 36% of subjects, 100-130 in 45%, 130-160 in 16%, and over 160mg/dl in 4%. The reduction rate of LDL-cholesterol was different between subjects whose LDL decreased below 100 and those whose LDL did not decrease below 130mg/dl, which suggests the existence of the individual difference of responsiveness to simvastatin. There were only 3 subjects (0.9%) who showed increase of liver enzyme over 3 times as the upper normal limit. Conclusion: Simvastatin is effective in improving lipid profiles in hypercholesterolemic Korean patients without serious side effects.
Apolipoproteins B
;
Cholesterol
;
Coronary Artery Disease
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Diabetes Mellitus
;
Diet Therapy
;
Female
;
Humans
;
Hypercholesterolemia
;
Hypertension
;
Individuality
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Korea
;
Liver
;
Male
;
Myocardial Ischemia
;
Simvastatin*
4.Korean multicenter clinical trial of simvastatin ( KS-1 study ).
Hyun Ho SHIN ; Kwon Bae KIM ; Jung Chaee KANG ; Min Soo SON ; Jae Hyung KIM ; Jong Seong KIM ; Seung Yun CHO ; Yung Woo SHIN ; Hyo Soo KIM ; In Ho CHAE ; Young Bae PARK ; Sung Choon CHOE ; Jung Don SEO ; Jong Hwa BAE ; Young Moo RHO ; Won Ro LEE ; Shung Chull CHAE ; Kwon Sam KIM ; Jung Chun AHN ; Cheol Ho KIM ; Jeong Euy PARK ; Cheol Whan LEE ; Jin Won JEONG ; Kyung Hoon CHOE ; Gil Ja SHIN ; Kun Joo RHEE ; Jae Ki KO ; Son Pyo HONG ; Un Ho RYOO ; Eun Seok JEON ; Dong Woon KIM ; Chong Yun RIM
Korean Journal of Medicine 1999;57(5):906-915
The aim of this study was to investigate the efficacy of simvastatin to improved lipid profiles in hypercholesterolemic Korean patients. METHODS: From 25 hospitals in Korea, 478 hypercholesterolemic patients were enrolled from November 1996 to April 1998. The inclusion criteria was hypercholesterolemia over 240 mg/dl after diet therapy for 1 month or hypercholesterolemia over 220 mg/dl in patients with definite evidence of ischemic heart disease. Simvastatin 10mg was started and doubled up to 40mg if total cholesterol level remained higher than 200 mg/dl at monthly check. Of 478 subjects, 344 patients in whom study protocol was not violated were analyzed. RESULTS: Male to female ratio was 27:73 and 47% of the subjects were in 6th decade. Hypertension, coronary artery disease, and diabetes mellitus were present in 30, 10, and 4% of the subjects. Baseline lipid profile (mean of total cholesterol-LDL-HDL-triglyceride mg/dl) was 274-185-52-188. The dose of simvastatin for 3 months was 10/10/10mg in 61% of subjects, 10/20/20mg in 21%, 10/10/20mg in 7%, and 10/20/40mg in 12%. The change of total cholesterol level(before-4wk-8wk-12wk-withdrawal 4wk) was 274-209- 205-198-250, and the maximal reduction rate was 27%. The change of LDL-cholesterol was 185-123-116-110-159, with maximal reduction rate 39%. The change of HDL-cholesterol was 52-54-56-55-54, with maximal increase rate 9%. The change of tryglyceride was 188-161- 164-162-189, with maximal reduction rate 15%. The value before/after treatment of ApoA1, ApoB, and Lp(a) was 129/129, 138/83, and 9.3/10.7, respectively. The level of LDL-cholesterol at the end of treatment was below 100mg/dl in 36% of subjects, 100-130 in 45%, 130-160 in 16%, and over 160mg/dl in 4%. The reduction rate of LDL-cholesterol was different between subjects whose LDL decreased below 100 and those whose LDL did not decrease below 130mg/dl, which suggests the existence of the individual difference of responsiveness to simvastatin. There were only 3 subjects (0.9%) who showed increase of liver enzyme over 3 times as the upper normal limit. Conclusion: Simvastatin is effective in improving lipid profiles in hypercholesterolemic Korean patients without serious side effects.
Apolipoproteins B
;
Cholesterol
;
Coronary Artery Disease
;
Diabetes Mellitus
;
Diet Therapy
;
Female
;
Humans
;
Hypercholesterolemia
;
Hypertension
;
Individuality
;
Korea
;
Liver
;
Male
;
Myocardial Ischemia
;
Simvastatin*