1.Influence of Antithyroid Antibodies in Euthyroid Women on IVF-ET Outcome.
Korean Journal of Fertility and Sterility 1997;24(1):143-151
The present study was designed to investigate if antithyroid antibodies (ATA) could affect the pregnancy outcome in euthyroid women undergoing in vitro fertilization and embryo transfer (IVF-ET). From October 1995 to September. 1996, 28 euthyroid women with ATA who underwent IVF-ET were studied. Fifty-one euthyroid women without ATA who underwent IVF-ET served as control. Thyroid peroxidase antibody (TPOA) and thyroglobulin antibody (TGA) were assayed using radio ligand assay kits as ATA. All patients included in study and control groups had only tubal factor in infertility. Long protocol of gonadotropin-releasing hormone agonist (GnRH-a) was used to. controlled ovarian hyperstimulation (COH) in all patients. There were no significant differences between study and control groups in patient characteristics such as age, infertility duration and hormonal profile. There were also no significant differences between two groups with respect to the clinical response to COH and IVF results such as number of retrieved oocytes, fertilization rate, number of embryos frozen and number of embryos transfered. There were no correlations between ATA (TPOA and TGA) titers and fertilization rate. The clinical pregnancy rate per cycle seemed to be lower in the study group than in the control group (26.3% vs 39.3%), but the difference was not statistically significant. The biochemical pregnancy rate per cycle and miscarriage rate were significantly higher in the study group at 18.4% (7/38) and 40.0% (4/10) compared with 5.6% (5/89) and 11.4% (4/35) in the control group. In the study group, both TPOA and TGA titers were significantly higher in the biochemical pregnancy group than in the clinical pregnancy group or non-pregnancy group. In 10 women with ATA who achieved pregnancy following IVF-ET, both TPOA and TGA titers were significantly higher in the miscarriage group than in the ongoing or delivery group. In conclusion, euthyroid women with ATA appear to represent a less favorable subset within other tubal factor patients when treated with IVF-ET.
Abortion, Spontaneous
;
Antibodies*
;
Embryo Transfer
;
Embryonic Structures
;
Female
;
Fertilization
;
Fertilization in Vitro
;
Gonadotropin-Releasing Hormone
;
Humans
;
Infertility
;
Iodide Peroxidase
;
Oocytes
;
Pregnancy
;
Pregnancy Outcome
;
Pregnancy Rate
;
Thyroglobulin
2.Treatment of Diabetic Nephropathy.
Korean Journal of Medicine 2005;68(5):594-597
No abstract available.
Diabetic Nephropathies*
3.Thyroid-specific Genes Transcription Factors.
Journal of Korean Society of Endocrinology 2002;17(3):312-324
No abstract available.
Transcription Factors*
4.Radioactive Iodine Therapy in Differentiated Tyroid Carcinoma.
Journal of Korean Society of Endocrinology 1999;14(4):627-635
No abstract available.
Iodine*
5.A Study on Apoptosis of HGPRT- Mouse Myeloma Cell Induced by Aminopterin, a de novo Pathway Blocking Agent.
Korean Journal of Immunology 1999;21(1):25-34
Programmed cell death (PCD), or apoptosis, plays an important role in embryonic development, metamorphsis, hormone-dependent atrophy and tumor growth, as a physiological event regulating the cell number or eliminating damaged cells. Currently hybridoma cell production, resulting from the fusion of myeloma cells with antibody producing spleen cells, is widely used in various fields of life science. This technique requires a hypoxanthine guanine phosphoribosyl transferase (HGPRT) deficient mutant myeloma cell line as a fusion partner. When these rnutant cells are treated with aminopterin plus hypoxanthine-thymidine (HAT) after the cell fusion they are selectively and efficiently eliminated so that one could get only fused hybridoma cells. But there hasn't been any report regarding this selective elimination mechanism of HGPRT mutant myeloma cell. By using HGPRT myeloma V653 as a model system this study demonstrated that PCD was induced by aminopterin treatment of this V653 cell. And this PCD was further characterized by cotreatement of cycloheximide, actinomycin-D, and calcium ionophore A23187 together with aminopterin. The apoptotic endonuclease involved in this PCD process was also detected and characterized. When V653 cells were incubated for the various periods of time in the presence of 0.4 uM aminopterin, the viability was continued to decrease until 48 hours of aminopterin treatment and there was no viable cell affer 36 hours of incubation. DNA fragmentation was detectable 3 hours of incubation and peaked between 12 and 18 hours of aminopterin treatment. The induction of cell death and DNA fragmentation of V653 cells by aminopterin were inhibited by protein synthesis inhibitor, cycloheximide, and RNA synthesis inhibitor, actinomycin-D and maximal inhibitory effects on cell death were seen at concentrations of 2 ug/ml and 0.5 uM, respectively. Ca2+ ionophore A23187 promoted aminopterin-induced cell death of V653. When the cells were coincubated with A23187 in the presence of aminopterin, cell viability was remarkably decreased at concentrations of more than 2 uM and DNA fragmentation was increased at concentrations of more than 0.2 uM. A23187 also induced cell death when the cells were treated with A23187 alone. When endogenous endonuclease activities of nuclei isolated from intact healthy cells and aminopterin-treated cells were compared for four different conditions, there were notable increases in the Ca2+/Mg2+ -independent and the Mg2+ -dependent endonuclease activity after incubation with aminopterin for 12 hours. In northern blot analysis, induction of c-myc gene was observed in aminopterin-treated V653 cell reached peak at 2 hours and thern decreased drastically.
Aminopterin*
;
Animals
;
Apoptosis*
;
Atrophy
;
Biological Science Disciplines
;
Blotting, Northern
;
Calcimycin
;
Calcium
;
Cell Count
;
Cell Death
;
Cell Fusion
;
Cell Line
;
Cell Survival
;
Cycloheximide
;
DNA Fragmentation
;
Embryonic Development
;
Female
;
Genes, myc
;
Guanine
;
Hybridomas
;
Hypoxanthine
;
Hypoxanthine Phosphoribosyltransferase
;
Mice*
;
Pregnancy
;
RNA
;
Spleen
;
Transferases
7.Clinical results of anterior repositioning splint
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons 1993;15(2):113-122
No abstract available.
Splints
8.Total knee arthroplasty in osteoarthritis.
Jung Man KIM ; Doo Hoon SUN ; Chang Hoon CHUNG
Journal of the Korean Knee Society 1993;5(1):22-28
No abstract available.
Arthroplasty*
;
Knee*
;
Osteoarthritis*
9.Clinical experiences in nasal tip plasty:elevation of tip.
Chung hoon LEE ; Keuk Shun SHIN
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1993;20(4):830-837
No abstract available.
10.Clinical Application of the Argon Laser in Dermatology.
Korean Journal of Dermatology 1987;25(3):373-378
The argon laser has been used in the treatment of a variety of cutaneous vascular and pigmented lesions. In 1983, authors reported on the therapeutic effect from argon laser treatment of nevus flammeus. This study was undertaken to evaluate the therapeutic effect and complication of the argon laser on many cutaneous lesions except nevus flammeus. The data of the 67 patients who were treated between November, 1984 and March, 1986 and could be followed up over 3 months at the Department of Dermatology, Seoul National University Hospital were analyzed. Patients were treated with Coherent Radiation Model No. 920 Laser with a spot size of 1 mm in diatemer. The pawer ranges were between 1.6 and 2.6 W using pulsed wave or continuous wave according to the size and the shape of the lesions. The argon laser is an effective modality in the treatment of superficial vascular lesions and especially when telangiectasia is prominent. In pigmented lesions, argon laser is effective for pigmented nevi excluding intradermal nevi and has been found effective in small sized nevus spilus and lentigines.
Argon*
;
Dermatology*
;
Humans
;
Lentigo
;
Nevus
;
Nevus, Intradermal
;
Nevus, Pigmented
;
Port-Wine Stain
;
Seoul
;
Telangiectasis