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1.
Zhonghua Yi Xue Za Zhi (Taipei) ; 64(4): 203-8, 2001 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11458757

RESUMO

BACKGROUND: Bone age (BA) estimation is one of the important applications of hand radiography in the area of pediatrics, especially for the diagnosis of endocrinological problems and growth disorders. BA estimation (BAE) is tedious, time-consuming and highly dependent upon the expert experience. Nowadays, most BAE standards are based on American standards, but there is no BAE standard for Taiwanese people. We attempt to construct a computerized BAE system to automate BAE and in the long run to build a BAE standard for Taiwanese. METHODS: Our BAE system is based on the carpal bone information. We propose a new 2-stage edge detection method for carpal bone feature extraction and a new method for locating the carpal bone region of interest. RESULTS: After the image is manually equalized, our BAE system can estimate the bone age automatically. The extracted carpal bone features were applied to three classifiers for age estimation: the weighted minimum distance, Bayes, and neural network classifiers. The Bayes and neural network classifiers had better results. In the 0.5-year tolerance case, they both had over 90% correct rate for both male and female training data. In the 1-year tolerance case, they could classify correctly for the male and female testing data. CONCLUSIONS: A computerized BAE system has been developed and some experiments have been conducted. It is found that the classifying results for 0.5-year tolerance are good and satisfactory.


Assuntos
Determinação da Idade pelo Esqueleto , Ossos do Carpo/diagnóstico por imagem , Feminino , Humanos , Masculino
2.
Contraception ; 47(6): 527-37, 1993 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-8334889

RESUMO

The ovarian effects of different doses of norethisterone (NET) were compared in 45 normally menstruating women in order to find the lowest effective dose of the Chinese NET "visiting pill". Subjects were randomly divided into 3 groups. Each subject in each group was taking 0.5, 1.5 or 3.0 mg per day from days 5 to day 18 of the cycle. Blood samples were taken on days 5, 8, 11, 14, 17, 20, 23, 26 and 29 of the cycle. Serum oestradiol (E2), progesterone (P), sex hormone binding globulin (SHBG), high density-lipoprotein cholesterol (HDL-C), and NET concentrations were measured. Ovulation, delayed ovulation, ovulation inhibition and follicular activity were classified by the analysis of the peripheral serum levels of sex hormones. Ovulation occurred in 7 women in the 0.5 mg group, in 2 women in the 1.5 mg group and in none of the 3.0 mg group. Mean serum SHBG levels were reduced progressively by 6.6% (Group 0.5), 15.5% (Group 1.5) and 23.4% (Group 3.0). There were no significant changes in HDL-C levels in any group. There was a significant correlation of mean serum NET concentrations with dose. The lack of complete inhibition of ovulation in most women in the 1.5 mg and 0.5 mg groups might suggest that the dose of NET required when used as a visiting pill could not be reduced below 3.0 mg.


PIP: In Shanghai, China, 45 25-35 year old women took a daily norethisterone (NET) "visiting pill" (vacation pills) on menstrual cycle days 5-18 as part of a clinical study comparing various doses of NET on ovarian function, sex hormone binding globulin (SHBG), and high density lipoprotein-cholesterol (HDL-C). The aim of the study was to determine the lowest effective dose of the NET visiting pill. Even though some ovarian activity occurred at all 3 doses (0.5, 1.5, and 3 mg), no woman experienced ovulation at 3 mg NET/day during days 5-18 of the cycle. It suppressed ovulation in 11 (73.3%) of the 15 women. Follicular activity occurred in the remaining 4 women. Ovulation occurred in 33% of women taking the 1.5 mg dose and in 66% of those taking the 0.5 mg dose. The higher the NET dose, the greater was the fall in mean serum SHBG levels from control levels (3 mg, 23.4%; 1.5 mg, 15.5%; and 0.5 mg, 6.6%). Both the regression equation and log dose regression equation showed a significant correlation between mean serum NET levels and dose (p .001). HDL-C levels remained basically the same as control levels. Since, at the 1.5 mg dose, ovulation occurred in 5 women and only 5 women experienced complete inhibition, a dose no lower than 3 mg should be used for the NET visiting pill.


Assuntos
HDL-Colesterol/sangue , Noretindrona/administração & dosagem , Ovário/fisiologia , Globulina de Ligação a Hormônio Sexual/metabolismo , Adulto , Estradiol/sangue , Feminino , Humanos , Noretindrona/sangue , Noretindrona/farmacologia , Ovário/efeitos dos fármacos , Ovulação/efeitos dos fármacos , Progesterona/sangue
3.
Contraception ; 45(6): 523-32, 1992 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-1535580

RESUMO

A randomised cross-over trial was performed to compare the pharmacodynamic actions of three low-dose oral contraceptives (OCs): Marvelon (150 micrograms desogestrel (DSG)+ 30 micrograms ethinyloestradiol (EE)), Mercilon (150 micrograms DSG + 20 micrograms EE) and Microgynon (150 micrograms levonorgestrel (LNG) + 30 micrograms EE). None of the OCs produced any significant changes in serum cholesterol, LDL-C and apoprotein B. Triglycerides were increased by the desogestrel OCs but not by Microgynon. The latter however increased the glucose and insulin responses to a glucose tolerance test whereas Marvelon and Mercilon had no effect. HDL-C increased with Marvelon, was unchanged with Mercilon and was decreased with Microgynon. Apoprotein AII was increased by all three OCs but only the DSG OCs increased apoprotein AI. All OCs produced similar increases in caeruloplasmin but the increase in SHBG was much greater with Marvelon and Mercilon than with Microgynon. Testosterone was reduced more with Microgynon than with the DSG OCs. Many of the changes reflect the strong anti-oestrogenic action of LNG on metabolic parameters compared to DSG. Except for the effect on HDL-C, there was little difference between Marvelon and Mercilon on metabolic parameters and this complements the findings from large-scale clinical trials of the two OCs. Mercilon, therefore provides a very satisfactory alternative to Marvelon.


PIP: 12 healthy volunteers attending the family planning clinic at Shanghai, First Maternity and Infant China, Hospital, enrolled in the study, Oral contraceptives (OCs) were prescribed: Marvelon (150 mcg of desogestrel--DSG), Mercilon (150 mcg of DSG), and Microgynon (150 mcg of levonorgestrel--LNG). The patients were divided into 6 groups of 2 persons each in a randomized cross-over study. OCs were taken on day 6 of the cycle up to day 21, then stopping for 7 days. Each OC was used for 3 months. During the pretreatment cycle between days 6 and 9 of the follicular phase and 21 and 22 of the luteal phase a blood sample was taken after fasting for determination of lipids, sex hormone binding globulin (SHGB), ceruloplasmin, and testosterone. After glucose loading, significant increases of glucose and insulin occurred at 1, 2, and 3 hours during treatment with Microgynon only. The ratio for total areas of insulin to glucose did not change significantly nor did glycosilated hemoglobin A1 levels. Serum triglyceride concentrations increased significantly for both Marvelon (27%-43%) and Mercilon (29-40%). Serum high density lipoprotein (HDL) cholesterol concentrations were significantly elevated with Marvelon but less so with Mercilon, while HDL-C decreased significantly with Microgynon. The serum low density lipoprotein (LDL) cholesterol changes were not significant, but LDL-C concentrations declined with DSG formulations and increased with Microgynon. Apoprotein A1 and A2 increased significantly for both Marvelon and Mercilon. Apoprotein A2 increased with Microgynon. Serum SHBG increased markedly with Marvelon (335-380%). Serum testosterone concentrations decreased significantly (33.2-40.4% with Microgynon) and so did ceruloplasmin values. The antiestrogenic effect of strong LNG in Microgynon produced significant metabolic changes. The effect of 30 mcg EE in Marvelon and 20 mcg EE of Mercilon was equal.


Assuntos
Glicemia/metabolismo , Anticoncepcionais Orais Combinados , Etinilestradiol , Insulina/sangue , Levanogestrel , Lipídeos/sangue , Norgestrel , Norpregnenos , Pancurônio/análogos & derivados , Congêneres da Progesterona , Adulto , Apolipoproteínas/sangue , Ceruloplasmina/análise , Colesterol/sangue , Desogestrel , Combinação Etinil Estradiol e Norgestrel , Feminino , Teste de Tolerância a Glucose , Humanos , Globulina de Ligação a Hormônio Sexual/análise , Testosterona/sangue , Triglicerídeos/sangue
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