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M D Krailo

Publications and source records attributed to M D Krailo.

59 records · Page 4Linked to original sources

Effects of reserpine on prolactin levels and incidence of breast cancer in postmenopausal women.

Epidemiological studies of reserpine use and breast cancer have generally found only small increases in breast cancer risk, even after long-term use. Prolactin levels in short-term reserpine users have been reported to be in the range of those of lactating women, levels which rodent experiments suggest should greatly increase breast cancer incidence. We measured prolactin levels in 15 women who had been taking reserpine-containing drugs for at least 5 years and compared them to levels in 15 women taking non-reserpine-containing antihypertensives and 15 women taking no antihypertensive medicines. Although reserpine users had significantly elevated levels of prolactin, their mean level was only approximately 50% greater than the mean level of the combined results from the two control groups. Based on a statistical model of breast cancer incidence, we calculate that such increases in prolactin in the postmenopausal period would be likely to cause only small increases in breast cancer risk, as have been observed in epidemiological studies.

Aged↗

Breast cancer in young women and use of oral contraceptives: possible modifying effect of formulation and age at use.

A case-control study of 314 breast cancer patients aged less than 37 at diagnosis and 314 individually matched controls was done to assess the influence of oral-contraceptive (OC) use on the risk of the disease. Long-term use before age 25 of combination-type OCs with a "high" content of the progestogen component was associated with increased risk of breast cancer: the relative risk was approximately 4 after 5 years of such use, and 9 cases and no controls had used such combination-type OCs for more than 6 years before age 25. Use of combination-type OCs with a "low" progestogen component appears to increase breast-cancer risk little or not at all.

Adult↗

'Hormonal' risk factors, 'breast tissue age' and the age-incidence of breast cancer.

For most cancer sites there is a linear log-log relationship between incidence and age. This relationship does not hold for breast cancer, and certain 'key' breast cancer risk factors suggest that breast tissue does not 'age' in step with calendar time. A quantitative description of 'breast tissue age' is suggested which brings the age-incidence curve of breast cancer into line with the common log-log cancers and explains quantitatively the known key risk factors. The model also explains the 'anomalous' finding that although early first birth is protective, late first birth carries a higher risk than nulliparity. US breast cancer rates are some four to six times the rates in Japan--the model suggests that the key risk factors, when considered jointly with weight, can explain about 85% of the difference.

Adolescent↗

Estimation of the distribution of age at natural menopause from prevalence data.

Nearly 30% of US women reach menopause (defined as cessation of menstrual periods) as a consequence of an operation. This biases the observable distribution of age at natural menopause. Another problem with estimating this distribution from a cross-sectional study is the clustering of reported age at natural menopause around ages ending in zero and five (Mac-Mahon B, Worcester J. Age at menopause, United States 1960-1962. Washington DC: National Center for Health Statistics, 1966. Vital and health statistics, Series 11: Data from the National Health Survey, no. 19. (DHEW publication no. (HSM) 66-1000)). This paper discusses the approach of Mac-Mahon and Worcester to this problem and compares it with a competing risks approach.

Adult↗