1.Relationship of Body Fat Percent with Serum Lipid Level and Blood Pressure in Adults.
Seock Whan LEE ; Tae Yoon HWANG ; Chang Yoon KIM
Korean Journal of Preventive Medicine 1995;28(4):783-794
This study was conducted to clarify the relationship of body fat percent with serum lipid level and blood pressure in adults. The study subjects were 472 men and l89 women who visited Multiphasic Health screening center of Yeungnam university Hospital in Taegu from May 20 to September 30, 1994. The relationship of serum lipid and blood pressure with BMl, Katsura index, atherogenic index, which calculated from the health screening data and body fat percent measured by impedance fat meter(model SIF-819) were analyzed. Three groups were classified as Group I(men: body fat percent > or= 20, women: body fat percent > or= 25, Group II (men: 15 < or = body fat percent <20, women: 20 < or = body fat percent<25, Group III(men: body fat percent <15. women: body fat percent<20) In this study, Group I accounted for 3.2%in men, 3.7%in women. Weight was significantly different among three groups in both sexes(p<0.01) and height was not significantly different among three groups. In men, serum total cholesterol, triglyceride, high density lipoprotein, low density lipoprotein. atherogenic index were significantly different(p<0.01). In women, serum total cholesterol and low density lipoprotein were significantly different(p<0.05 but there was no differences in triglyceride and high density lipoprotein among three groups. BMl and Katsura index were significantly different among three groups in both sexes(p<0.01). In men, body fat percent was positively correlated with weight, BMl, Katsura index, total cholesterol, triglyceride, low density lipoprotein, atherogenic index and systolic and diastolic blood pressures, and negatively correlated with high density lipoprotein. In women, body fat percent was positively correlated with age, height, weight, BMl, Katsura index, total cholesterol, triglyceride, low density lipoprotein and atherogenic index, and negatively correlated with high density lipoprotein. But there was no significant correlation between body fat percent and blood pressure in women. In multiple regression analysis for total cholesterol, fat percent, age and BMl were significant independent variables in men(p<0.05, R2=0.1286), and body fat percent and age in women(p<0.05, R2=0.3399). In case of LDL/HDL ratio, only BMl was a significant independent variable in men(p<0.01, R2=0.0954), and body fat percent, age and BMl in women(p<0.05, R2=0.3164). In multiple regression analysis, age, low density lipoprotein and total cholesterol were significant independent variables on systolic blood pressure in men(p<0.05, R2=0.1297), age and total cholesterol in women(p<0.055, R2=0.1705). On diastolic blood pressure, only age was a significantly independent variable in men(p<0.01, R2=0.0972) and women(p<0.01, R2=0..1218). From the result of this study, it could concluded that body fat percent was significantly associated with other obesity indices and serum lipid, but had no significant association with blood pressure. To establish the relationship of body fat percent with blood pressure, further study which consider other variables that may have an effect on blood pressure should be performed.
Adipose Tissue*
;
Adult*
;
Blood Pressure*
;
Cholesterol
;
Daegu
;
Electric Impedance
;
Female
;
Humans
;
Lipoproteins
;
Male
;
Mass Screening
;
Obesity
;
Triglycerides
2.Cloning and Sequencing of the phoA Gene which is Regulated by the phoP-phoQ operon in Pathogenic Enteric Bacteria.
Yeungnam University Journal of Medicine 1995;12(2):237-245
The DNA fragment containing the phoA of Klebsiella pneumoniae was cloned into pACYC184. The size of the insert. was 4.0 kb and the restriction map showed it contained 3 Pstl sites and 4 PvuLI sites. The nucleotide sequence of the phoA region was determined, which showed strong (80%) sequence similarity with that of Escherichia coli. This suggested that these two species are phylogenetically very close to each other.
Base Sequence
;
Clone Cells*
;
Cloning, Organism*
;
DNA
;
Enterobacteriaceae*
;
Escherichia coli
;
Klebsiella pneumoniae
;
Operon*
3.DNA Diagnosis Using Polymerase Chain Reaction.
Yeungnam University Journal of Medicine 1991;8(2):13-23
No abstract available.
Diagnosis*
;
DNA*
;
Polymerase Chain Reaction*
4.Analysis of gene products induced by phosphate starvation in enteric bacteria.
In A DOH ; Tae Yoon LEE ; Sung Kwang KIM
Journal of the Korean Society for Microbiology 1992;27(6):517-524
No abstract available.
Enterobacteriaceae*
;
Starvation*
5.Subtotal nasal reconstruction by the scalping flap technique.
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1993;20(6):1273-1283
No abstract available.
Scalp*
6.Plastic operation method of traumatic finger tip and nail deformity.
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1991;18(2):349-355
No abstract available.
Congenital Abnormalities*
;
Fingers*
;
Plastics*
7.Neuropeptide Y(NPY)-immunoreactive neuronal changes in senile dementia of alzheimer type(SDAT).
Korean Journal of Physical Anthropology 1993;6(2):249-261
No abstract available.
Alzheimer Disease*
;
Neurons*
;
Neuropeptides*
8.Clinical study of transaxillary subpectoral augmentation mammoplasty.
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1992;19(4):656-664
No abstract available.
Female
;
Mammaplasty*
9.THE CONCEPT OF MULTIPLAN DISSECTION IN RECONSTRUCTIVE AND AESTHETIC BREAST IMPLANT SURGERY.
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1997;24(6):1501-1507
No abstract available.
Breast Implants*
;
Breast*
10.Genomic analysis of Mycobacterium foruitum by pulsed-filed gel electrophoresis.
Tae Yoon LEE ; In A DO ; Sung Kwang KIM
Yeungnam University Journal of Medicine 1995;12(2):366-385
Epidemiological studies are important in both the prevention and treatment of mycobacterial infections. This study was initiated to establish the pulsed-field gel electrophoresis (PFGE) method, which are not yet extensively studied. The most apprpriate restriction endonucleases included Dral, AsnI, and XbaI. The optimal PFGE condition was different according to the enzymes used. Two stage PFGE was performed, in case of DraI first stage was performed with 10 seconds of initial pulse and 15 seconds of findA pulse, while the second stage was performed with 60 seconds of initial pulse and 70 seconds of final pu',se. The electrophoresis time for DraI-PFGE was 14 hours for each stage. Electrophoresis was performed for 22 hours, in case of XbaI, with 3 seconds of initial pulse and 12 seconds of final pulse. Electrophoresis was performed for 22 hours, in case of AsnI, with 5 seconds of initial pulse and 25 seconds of final pulse. In all cases the voltage of the electrophoresis was maintained constantly at 200 voltage. Standard mycobacterial strains, which included Mycobacterium bovis BCG, M. tuberculosis, and M. fortuitum, could not be differentiated by PFGE analysis. PFGE analysis was performed to differentiate 9 clinically isolated M. fortuitum strains using AsnI. All M. fortuitum strains showed different genotypes except 2 strains. Cluster analysis divided M. fortuitum strains into 2 large groups. PFGE analysis was performed to further differentiate M. fortuitum isolates using XbaI. The undifferentiated 2 M. fortuitum strains showed different PFGE patterns with Xba I. Cluster analysis of the XbaI-PFGE patterns showed more complex grouping than AsnI-PFGE patterns, which showed that XbaI-PFGE analysis was better than AsnI-PFGE in M. fortuitum genotyping. The top dissimilarity values of AsnI-PFGE and XbaI-PFGE were 0.74 and 0.75, respectively. This value was higher than that of arbitrarily primed polymerase chain reaction (AP-PCR) analysis and lower than that of restriction fragment length polymorphism (RFLP) analysis. This suggested that PFGE can be used as a supportive or alternative genotyping method to RFLP analysis.
DNA Restriction Enzymes
;
Electrophoresis*
;
Electrophoresis, Gel, Pulsed-Field
;
Epidemiologic Studies
;
Genotype
;
Mycobacterium bovis
;
Mycobacterium*
;
Polymerase Chain Reaction
;
Polymorphism, Restriction Fragment Length
;
Tuberculosis