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Galactose consumption, metabolism, and follicle-stimulating hormone concentrations in women of late reproductive age
To test the hypothesis that high galactose consumption and low activity of galactose-1-phosphate uridyl transferase (transferase) is associated with early ovarian senescence among nongalactosemic women. Cross-sectional study. Data collection consisted of a self-administered questionnaire with sectio...
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Published in: | Fertility and sterility 1994-12, Vol.62 (6), p.1168-1175 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Request full text |
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Summary: | To test the hypothesis that high galactose consumption and low activity of galactose-1-phosphate uridyl transferase (transferase) is associated with early ovarian senescence among nongalactosemic women.
Cross-sectional study. Data collection consisted of a self-administered questionnaire with sections on diet (food frequency data to measure galactose consumption), reproductive, and medical histories. One blood sample was collected to measure FSH and transferase activity; FSH was used as a measure of ovarian senescence. Among women who were having menstrual periods at least every 8weeks, the blood sample was drawn in the early follicular phase (days 2 to 4) of a menstrual cycle.
Two hundred ninety-five women volunteers ages 38 to 49years who had not had a hysterectomy or oophorectomy were recruited through posters and advertisements.
Serum FSH concentrations.
Controlling for age, smoking, and body mass, transferase activity and FSH were unrelated. However, FSH levels were 29% higher (95% confidence intervals, 9% to 52%) among women who reported consuming ≥6g galactose/d.
These data do not support the hypothesis that low transferase activity represents a genetic predisposition for early ovarian senescence, as measured by FSH levels in women ages 38 to 49years. However, the hypothesized positive association between galactose consumption and FSH was supported. |
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ISSN: | 0015-0282 1556-5653 |
DOI: | 10.1016/S0015-0282(16)57180-5 |