1.Age Changes and Sex Differences in Serum Dehydroepiandrosterone Sulfate (DHEAS) Concentrations & its related factors throughout Adulthood .
Chul Young BAE ; Seok Kie LEE ; Young Jin LEE ; Ho Taeg LEE ; Young Gon LEE
Journal of the Korean Geriatrics Society 1998;2(2):46-57
BACKGROUND : DHEAS, the major circulating adrenal hormone, has been suggested to have a role in many aging related diseases and perhaps in aging itself. But, there is no epidemiologic data of DHEAS in normal adults in Korea. We studied age changes and sex differences in serum DHEAS & its related factors throughout adulthood. METHODS : We administ structured questionnaires to the study subjects. We measured serum DHEAS levels and several biochemical markers (total cholesterol, triglyceride, HDL-cholesterol, glucose etc) in 1.710 healthy men(857) and women (853), aged 17-76 years. We also measured their height, weight, waist & hip circumference and body fat contents with bioimpedance method. We analyzed various variables relating to serum DHEAS levels by using SPSS. Reference data of serum DHEAS level in normal adults were also suggested. RESULTS : The DHEAS concentration peaked at age group blow age of 30 years in man(260.9 microgram/dL). Then mean values declined steadily in both sexes (r=-0.38, p<0.001 in men and r=-0.46, p<0.001 in women). At age group above 70 years, only 30.9% in men & 30.4% in women, when compared with age group below 30 years, was remained. DHEAS concentration were significantly higher in men than women at all age group except age group above 70 years. Average 1.5 times higher concentration in men than in women (at least 1.28 times at age<30 and max 2.00 times at age 60-64). In men, DHEAS had higher mean value in smokers (218.1 vs 199.1 microgram/dL, p<0.05), drinkers (>or=2 times/week, 219.1 vs 185.3 microgram/dL, p<0.01), android type fat distribution group (waist/hip>0.85, 227.1 vs 197.4 microgram/dL) after adjusting age. DHEAS was positively correlated with body mass index (r=0.12, p<0.01). But in women, drinkers (154.3 vs 131.7 microgram/dL, p<0.05) and regular exercise group (146.1 vs 131.6 microgram/dL, p=0.05) had higher mean DHEAS value. There were no significant association between DHEAS and lipid profile (total cholesterol, triglyceride, HDL-cholesterol, LDL-cholesterol) & fasting glucose level in both sex. CONCLUSION : Our data suggest that DHEAS levels may influenced by several sociodemographic factors (e.g. smoking, alcohol, exercise etc) and body mass index. DHEAS level was inversely correlated by age in both sex and men had 1.5 times higher DHEAS values than women. We could not find any association between DHEAS level and lipid profile & fasting blood sugar.
Adipose Tissue
;
Adult
;
Aging
;
Biomarkers
;
Blood Glucose
;
Body Mass Index
;
Cholesterol
;
Dehydroepiandrosterone Sulfate*
;
Dehydroepiandrosterone*
;
Fasting
;
Female
;
Glucose
;
Hip
;
Humans
;
Korea
;
Male
;
Surveys and Questionnaires
;
Sex Characteristics*
;
Smoke
;
Smoking
;
Triglycerides
;
Waist-Hip Ratio
2.Two Cases of Massive Ovarian Edema.
Young Gyu LEE ; Sam Bong KIM ; Heung Gon KIM ; Weon Cheol HAN ; Hyung Bae MOON
Korean Journal of Gynecologic Oncology and Colposcopy 1994;5(2):98-103
Massive ovarian deema is a tate conditian. It is a benign enlargement of the ovary caused by accumulation of fluid, which is thought to result from intermittent partial toraion of the ovarian pedicle. Histologically, the ovaries were characterized by diffuse edema of medulla and inner cortex. Two cases of massive ovanan edema are reported with brief review of the literatures.
Edema*
;
Female
;
Ovary
3.Hamartoma Arising in the Urinary Bladder: A case report.
Young Bae KIM ; Tae Sook HWANG ; Byung Gon PARK ; Jin Sook JEONG ; Sook Hee HONG
Korean Journal of Pathology 1993;27(3):283-286
Hamartoma of the bladder is quite a rare entity which is composed of a disorderly admixture of mature cellular elements normally present in the urinary bladder. There is a great controversy regarding the pathogenesis of this lesion. Whether it is a true hamartomatous lesion or metaplastic lesion developed secondary to the inflammatory process. Similar or identical lesions has often been given by other names such as florid examples of cystitis glandularis. We prefer to cell florid examples of cystitis glandularis rather than hamartoma when it was occurred in an old age higher then 50th decade. Here we report a case of hamartoma of the urinary bladder in 44 years old man. Cystoscopic examination revealed a papillary polypoid mass which was attached to the fundus of bladder by long stalk. The mass measured 1.5 cm in greatest diameter. It was composed of epithelial nests resembling von Brunn's nest, cystitis glandularis or cystitis cystica dispersed in a stroma rich in smooth muscle and fibrous tissue.
Hamartoma
4.Comparison of marginal microleakage between low and high flowable resins in class V cavity.
Sang Bae BAE ; Young Gon CHO ; Myeong Seon LEE
Journal of Korean Academy of Conservative Dentistry 2009;34(6):477-483
The purpose of this study was to compare the microleakage of low and high viscosity flowable resins in class V cavities applied with 1-step adhesives. Forty class V cavities were prepared on the cervices of buccal and lingual surfaces of extracted molar teeth and divided into four groups (n=8). Cavities were restored with AQ Bond Plus/Metafil Flo alpha, G-Bond/UniFil LoFlo Plus (Low flow groups), AQ Bond Plus/Metafil Flo and G-Bond/UniFil Flow (High flow group), respectively. Specimens were immersed in a 2% methylene blue solution for 24 hours, and bisected longitudinally. They were observed microleakages at the enamel and dentinal margins. In conclusion, the low viscosity flowable resins showed lower marginal microleakage than do the high viscosity flowable resins in class V cavities.
Dental Enamel
;
Dentin
;
Dentin-Bonding Agents
;
Methylene Blue
;
Molar
;
Tooth
;
Viscosity
5.Low-frequency Mosaicism of Trisomy 14, Missed by Array CGH.
Cha Gon LEE ; Jun No YUN ; Sang Jin PARK ; Young Bae SOHN
Journal of Genetic Medicine 2013;10(1):52-56
Mosaic trisomy 14 syndrome is a well-known but unusual chromosomal abnormality with a distinct and recognizable phenotype. Array comparative genomic hybridization (CGH) analysis has recently become a widely used method for detecting DNA copy number changes, in place of traditional karyotype analysis. However, the array CGH shows a limitation for detecting the low-level mosaicism. Here, we report the detailed clinical and cytogenetic findings of patient with low-frequency mosaic trisomy 14, initially considered normal based on usual cut-off levels of array CGH, but confirmed by G-banding karyotyping. Our patient had global developmental delay, short stature, congenital heart disease, craniofacial dysmorphic features, and dark skin patches over her whole body. Estimated mosaicism proportion was 23.3% by G-banding karyotyping and 18.0% by array CGH.
Chromosome Aberrations
;
Chromosomes, Human, Pair 14
;
Comparative Genomic Hybridization
;
Cytogenetics
;
DNA Copy Number Variations
;
Heart Diseases
;
Humans
;
Hypogonadism
;
Intellectual Disability
;
Karyotype
;
Karyotyping
;
Mitochondrial Diseases
;
Mosaicism
;
Ophthalmoplegia
;
Phenotype
;
Skin
;
Trisomy
6.Clinicopathologic Findings of Early Gastic Cancer.
Young Bae KO ; Won Gon KIM ; Joon Mee KIM
Journal of the Korean Cancer Association 1999;31(1):62-71
PURPOSE: The prognosis forearly gastric cancer (EGC) is generally excellent after curative gastrectomy alone. However, the EGC of young patients was generally more invasive and metastasizing, and the prognosis of them was poorer than those of the elderly. We performed a retrospective study to evaluate clinica1 and pathological factors influencing the prognosis of EGC. MATERIALS AND METHODS: The authors investigated 66 cases of EGC resected at Inha Hospital in Song-Nam, from January 1987 to December 1996. We analyzed 9 clinicopathologic factors: age, sex, macroscopic type, tumor size, depth of invasion, location, lymph node metastasis, Williss classification and Laurens classification. RESULTS: Out of 66 cases (42 males, 24 females) of EGC, the sex ratio (M: F) was 1.75: 1, and the mean age was 55.5 years in male and 54.3 in female. The age incidence revealed a greater prevalence on 6th decade (33.3%). The most common macroscopic type of EGC was IIb and its combined type (43 cases, 65.2%). In tumor size, 16 cases (24.2%) were between 2.0 and 2.9 cm, and 13 cases (19.6%) between 1.0 and 1.9 cm, 10 cases (15%) between 3.0 and 3.9 cm. The tumors smaller than 2.0 cm were 33.2% but greater than 5.0 cm were 18.8%. In male, mucosal lesions were more common (66.6%) than submucosal lesions (33.4%); but in female, the incidence of both types of lesions were the same. The submucosal lesion in female was the most frequent at 4th decade. The major location of EGC was antrum (51.5%). Lymph node metastases were found in 3 females and 1 male. By Williss classification, poorly differentiated adenocarcinoma and signet ring cell carcinoma were more common in female (29.2%, 25%) than in male (11.9%, 14.3%). By Laurens classification, the diffuse type was more common in female (50%) than in male (33.3%). This type was the most frequent in 4th decade female patients. However, none of the above data reached statistical significance. CONCLUSION: We found the generalized tendency, though not statistically confinned, that the young female patients of EGC frequently had larger and poorly differentiated, diffuse adenocarcinomas with more frequent lymph node metastasis than male. The authors emphasizes that a further study would be needed in young female patients of EGC on hormonal factors influencing its clinicopathologic findings.
Adenocarcinoma
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Aged
;
Carcinoma, Signet Ring Cell
;
Classification
;
Female
;
Gastrectomy
;
Humans
;
Incidence
;
Lymph Nodes
;
Male
;
Neoplasm Metastasis
;
Prevalence
;
Prognosis
;
Retrospective Studies
;
Sex Ratio
;
Stomach Neoplasms
7.Risk factors of delirium in elderly inpatients.
Seong Wook HWANG ; Seong Wook KANG ; Young Gon KANG ; Seung Gon CHOI ; Jin LEE ; Moon Jong KIM ; Young Jin LEE ; Chul Young BAE
Journal of the Korean Academy of Family Medicine 2002;23(1):112-121
BACKGROUND: This study was done to investigate the clinical risk factors of delirium in general hospital's elderly inpatients. METHODS: A case-control study design was used. Forty cases and age -sex matched 120 contols were identified using hospital discharge data from June 1995 to May 2001. The controls were selected during the same period. The clinical records of each subject were reviewed using discharged disease code to select cases. Subsequent7, the data were recorded from clinical records. RESULTS: The subjects admitted with delirium tended to have increased age (P=0.007), hypoxia(P=0.018), low hemoglobin(P =0.011),sleep disturbance (P=0.001), more ADL total dependence ( P=0.018), diagnoses with infections (P=0.006), diabetes (P=0.046), and hypertension (P=0.041). Above risk factors seemed to be clinically associated with delirium. CONSLUSION: These findings indicate that rapid infection control, maintenance of good sleep hygiene, well-controlled diabetes and hypertension, and correction of hypoxia may help to prevent delirium in general hospital's elderly inpatients.
Activities of Daily Living
;
Aged*
;
Anoxia
;
Case-Control Studies
;
Delirium*
;
Diagnosis
;
Humans
;
Hygiene
;
Hypertension
;
Infection Control
;
Inpatients*
;
Risk Factors*
8.Reciprocal Deletion and Duplication of 17p11.2-11.2: Korean Patients with Smith-Magenis Syndrome and Potocki-Lupski Syndrome.
Cha Gon LEE ; Sang Jin PARK ; Jun No YUN ; Shin Young YIM ; Young Bae SOHN
Journal of Korean Medical Science 2012;27(12):1586-1590
Deletion and duplication of the -3.7-Mb region in 17p11.2 result in two reciprocal syndrome, Smith-Magenis syndrome and Potocki-Lupski syndrome. Smith-Magenis syndrome is a well-known developmental disorder. Potocki-Lupski syndrome has recently been recognized as a microduplication syndrome that is a reciprocal disease of Smith-Magenis syndrome. In this paper, we report on the clinical and cytogenetic features of two Korean patients with Smith-Magenis syndrome and Potocki-Lupski syndrome. Patient 1 (Smith-Magenis syndrome) was a 2.9-yr-old boy who showed mild dysmorphic features, aggressive behavioral problems, and developmental delay. Patient 2 (Potocki-Lupski syndrome), a 17-yr-old boy, had only intellectual disabilities and language developmental delay. We used array comparative genomic hybridization (array CGH) and found a 2.6 Mb-sized deletion and a reciprocal 2.1 Mb-sized duplication involving the 17p11.2. These regions overlapped in a 2.1 Mb size containing 11 common genes, including RAI1 and SREBF.
Adolescent
;
Asian Continental Ancestry Group/*genetics
;
Child, Preschool
;
*Chromosomes, Human, Pair 17
;
Comparative Genomic Hybridization
;
Developmental Disabilities/etiology/genetics
;
Gene Deletion
;
Gene Duplication
;
Humans
;
Intellectual Disability/etiology/genetics
;
Karyotyping
;
Male
;
Smith-Magenis Syndrome/diagnosis/*genetics
;
Sterol Regulatory Element Binding Protein 1/genetics
;
Transcription Factors/genetics
9.Array-Based Comparative Genomic Hybridization in 190 Korean Patients with Developmental Delay and/or Intellectual Disability: A Single Tertiary Care University Center Study.
Cha Gon LEE ; Sang Jin PARK ; Jun No YUN ; Jung Min KO ; Hyon Ju KIM ; Shin Young YIM ; Young Bae SOHN
Yonsei Medical Journal 2013;54(6):1463-1470
PURPOSE: This study analyzed and evaluated the demographic, clinical, and cytogenetic data [G-banded karyotyping and array-based comparative genomic hybridization (array CGH)] of patients with unexplained developmental delay or intellectual disability at a single Korean institution. MATERIALS AND METHODS: We collected clinical and cytogenetic data based on retrospective charts at Ajou University Medical Center, Suwon, Korea from April 2008 to March 2012. RESULTS: A total of 190 patients were identified. Mean age was 5.1+/-1.87 years. Array CGH yielded abnormal results in 26 of 190 patients (13.7%). Copy number losses were about two-fold more frequent than gains. A total of 61.5% of all patients had copy number losses. The most common deletion disorders included 22q11.2 deletion syndrome, 15q11.2q12 deletion and 18q deletion syndrome. Copy number gains were identified in 34.6% of patients, and common diseases among these included Potocki-Lupski syndrome, 15q11-13 duplication syndrome and duplication 22q. Abnormal karyotype with normal array CGH results was exhibited in 2.6% of patients; theses included balanced translocation (n=2), inversion (n=2) and low-level mosaicism (n=1). Facial abnormalities (p<0.001) and failure to thrive were (p<0.001) also more frequent in the group of patients with abnormal CGH findings. CONCLUSION: Array CGH is a useful diagnostic tool in clinical settings in patients with developmental delay or intellectual disability combined with facial abnormalities or failure to thrive.
Adolescent
;
Adult
;
Child
;
Child, Preschool
;
Comparative Genomic Hybridization/*methods
;
Female
;
Gene Dosage/genetics
;
Humans
;
Infant
;
Intellectual Disability/*genetics
;
Karyotype
;
Male
;
Republic of Korea
;
Retrospective Studies
;
Tertiary Healthcare/statistics & numerical data
;
Young Adult
10.Removal of Dislodged Stent by Using 8 Fr Sheath and Forcep during Transradial Coronary Stenting.
Jin Gon PARK ; Moo Hyun KIM ; Young Jin BAE ; Soo Hoon LEE ; Kwang Soo CHA ; Chang Ho YANG ; Young Dae KIM ; Jong Seong KIM
Korean Circulation Journal 2000;30(10):1312-1315
Stent dislogement or migration is not a rare complication. Its incidence varies from 1.4% to 8% of the cases. When stent migration occurs, the usual treatment or management is to implant stent in the distal peripheral artery or proximal coronary artery. But, probably the best treatment is safe retrieval of the dislodged stent. During the transfemoral coronary intervention, undeployed stent can be more easily retrieved into the guiding catheter with relatively larger guiding catheter luminal space. Also, larger sheath can be changed more easily when the retrieval of stent is difficult. In the transradial coronary stenting, usual size of guiding catheter is 6 Fr, makes it difficult to retrieve relatively bulky stent when deployment of stent fails. We report 2 cases of stent dislodgment during transradial coronary stenting which can be successfully removed by using myocardial biopsy forcep through 8 Fr sheath. These combination could be one of the valuable methods, especially during transradial stenting.
Arteries
;
Biopsy
;
Catheters
;
Coronary Vessels
;
Incidence
;
Phenobarbital
;
Stents*
;
Surgical Instruments*