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1.
N Engl J Med ; 365(14): 1304-14, 2011 Oct 06.
Article in English | MEDLINE | ID: mdl-21991952

ABSTRACT

BACKGROUND: Before 1971, several million women were exposed in utero to diethylstilbestrol (DES) given to their mothers to prevent pregnancy complications. Several adverse outcomes have been linked to such exposure, but their cumulative effects are not well understood. METHODS: We combined data from three studies initiated in the 1970s with continued long-term follow-up of 4653 women exposed in utero to DES and 1927 unexposed controls. We assessed the risks of 12 adverse outcomes linked to DES exposure, including cumulative risks to 45 years of age for reproductive outcomes and to 55 years of age for other outcomes, and their relationships to the baseline presence or absence of vaginal epithelial changes, which are correlated with a higher dose of, and earlier exposure to, DES in utero. RESULTS: Cumulative risks in women exposed to DES, as compared with those not exposed, were as follows: for infertility, 33.3% vs. 15.5% (hazard ratio, 2.37; 95% confidence interval [CI], 2.05 to 2.75); spontaneous abortion, 50.3% vs. 38.6% (hazard ratio, 1.64; 95% CI, 1.42 to 1.88); preterm delivery, 53.3% vs. 17.8% (hazard ratio, 4.68; 95% CI, 3.74 to 5.86); loss of second-trimester pregnancy, 16.4% vs. 1.7% (hazard ratio, 3.77; 95% CI, 2.56 to 5.54); ectopic pregnancy, 14.6% vs. 2.9% (hazard ratio, 3.72; 95% CI, 2.58 to 5.38); preeclampsia, 26.4% vs. 13.7% (hazard ratio 1.42; 95% CI, 1.07 to 1.89); stillbirth, 8.9% vs. 2.6% (hazard ratio, 2.45; 95% CI, 1.33 to 4.54); early menopause, 5.1% vs. 1.7% (hazard ratio, 2.35; 95% CI, 1.67 to 3.31); grade 2 or higher cervical intraepithelial neoplasia, 6.9% vs. 3.4% (hazard ratio, 2.28; 95% CI, 1.59 to 3.27); and breast cancer at 40 years of age or older, 3.9% vs. 2.2% (hazard ratio, 1.82; 95% CI, 1.04 to 3.18). For most outcomes, the risks among exposed women were higher for those with vaginal epithelial changes than for those without such changes. CONCLUSIONS: In utero exposure of women to DES is associated with a high lifetime risk of a broad spectrum of adverse health outcomes. (Funded by the National Cancer Institute.).


Subject(s)
Breast Neoplasms/chemically induced , Diethylstilbestrol/adverse effects , Estrogens, Non-Steroidal/adverse effects , Genital Neoplasms, Female/chemically induced , Pregnancy Complications/chemically induced , Prenatal Exposure Delayed Effects , Adenocarcinoma, Clear Cell/chemically induced , Female , Follow-Up Studies , Humans , Menopause, Premature , Pregnancy , Stillbirth , Uterine Cervical Dysplasia/chemically induced
2.
J Rheumatol ; 37(10): 2167-73, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20634240

ABSTRACT

OBJECTIVE: Animal studies have suggested that prenatal diethylstilbestrol (DES) exposure may alter immune system development and function including antigen self-recognition. A cohort study was conducted to investigate whether prenatal DES exposure might influence the incidence of at least some specific autoimmune diseases in women. METHODS: A group of women who were and were not prenatally exposed to DES have been followed for more than 25 years for numerous health outcomes including autoimmune disease. To verify diagnoses, medical records or physician abstracts were requested for all women who reported a diagnosis of rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), optic neuritis (ON), and idiopathic thrombocytopenic purpura (ITP). Incidence rates of these autoimmune diseases were compared between women who were and who were not prenatally DES-exposed. RESULTS: Overall, there was no increase in verified autoimmune disease among DES-exposed women relative to those who were not exposed (RR 1.2; 95% CI 0.7, 2.1). There was, however, a positive association between prenatal DES exposure and RA among women younger than 45 years (RR 4.9; 95% CI 1.1, 21.6) and an inverse association among women who were 45 years and older (RR 0.1; 95% CI 0.01, 0.7). CONCLUSION: Overall, these data provide little support for an association between prenatal DES exposure and development of autoimmune disease. The implication that such exposure may be related to RA in an unusual age-related manner is based on small numbers of cases and warrants further study.


Subject(s)
Autoimmune Diseases/etiology , Diethylstilbestrol/adverse effects , Estrogens, Non-Steroidal/adverse effects , Prenatal Exposure Delayed Effects , Adult , Animals , Arthritis, Rheumatoid/etiology , Cohort Studies , Female , Humans , Middle Aged , Pregnancy , Risk Factors , Surveys and Questionnaires , Young Adult
3.
Environ Health ; 8: 37, 2009 Aug 18.
Article in English | MEDLINE | ID: mdl-19689815

ABSTRACT

BACKGROUND: Diethylstilbestrol (DES), a synthetic estrogen widely prescribed to pregnant women during the 1940s70s, has been shown to cause reproductive problems in the daughters. Studies of prenatally-exposed males have yielded conflicting results. METHODS: In data from a collaborative follow-up of three U.S. cohorts of DES-exposed sons, we examined the relation of prenatal DES exposure to occurrence of male urogenital abnormalities. Exposure status was determined through review of prenatal records. Mailed questionnaires (1994, 1997, 2001) asked about specified abnormalities of the urogenital tract. Risk ratios (RR) were estimated by Cox regression with constant time at risk and control for year of birth. RESULTS: Prenatal DES exposure was not associated with varicocele, structural abnormalities of the penis, urethral stenosis, benign prostatic hypertrophy, or inflammation/infection of the prostate, urethra, or epididymus. However, RRs were 1.9 (95% confidence interval 1.13.4) for cryptorchidism, 2.5 (1.54.3) for epididymal cyst, and 2.4 (1.54.4) for testicular inflammation/infection. Stronger associations were observed for DES exposure that began before the 11th week of pregnancy: RRs were 2.9 (1.65.2) for cryptorchidism, 3.5 (2.06.0) for epididymal cyst, and 3.0 (1.75.4) for inflammation/infection of testes. CONCLUSION: These results indicate that prenatal exposure to DES increases risk of male urogenital abnormalities and that the association is strongest for exposure that occurs early in gestation. The findings support the hypothesis that endocrine disrupting chemicals may be a cause of the increased prevalence of cryptorchidism that has been seen in recent years.


Subject(s)
Diethylstilbestrol/adverse effects , Estrogens, Non-Steroidal/adverse effects , Maternal Exposure/adverse effects , Prenatal Exposure Delayed Effects/chemically induced , Urogenital Abnormalities/chemically induced , Abnormalities, Drug-Induced/epidemiology , Adult , Cohort Studies , Cryptorchidism/chemically induced , Cryptorchidism/epidemiology , Female , Follow-Up Studies , Gestational Age , Humans , Male , Middle Aged , Nuclear Family , Odds Ratio , Pregnancy , Prenatal Exposure Delayed Effects/epidemiology , Proportional Hazards Models , Risk , Surveys and Questionnaires , United States/epidemiology , Urogenital Abnormalities/epidemiology , Young Adult
4.
J Womens Health (Larchmt) ; 18(4): 547-52, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19361323

ABSTRACT

PURPOSE: To determine if women exposed in utero to diethylstilbestrol (DES) are more likely than unexposed women to receive recommended or additional breast cancer screening examinations. METHODS: 1994 Diethylstilbestrol-Adenosis (DESAD) cohort data are used to assess the degree of recommended compliance of breast cancer screenings found in 3140 DES-exposed and 826 unexposed women. Participants were enrolled at four sites: Houston, Boston, Rochester, and Los Angeles. Logistic regression modeling was used to analyze mailed questionnaire data that included reported frequency over the preceding 5 years (1990-1994) of breast-self examinations (BSEs), clinical breast examinations (CBEs), and mammograms. RESULTS: DES-exposed women exceeded annual recommendations for CBEs (aOR 2.20, 95% CI, 1.04-4.67) among women without a history of benign breast disease (BBD) compared with unexposed women. There were no other statistically significant differences between exposed and unexposed women who reported performing BSEs, CBEs (<40 years of age), and mammographies, regardless of BBD history. CONCLUSIONS: The majority of DES-exposed women receive breast cancer screenings at least at recommended intervals, but over two thirds do not perform monthly BSEs. Future efforts should be focused on further educating this and other at-risk populations through mailed reminders and during patient consultations on the benefits of screening examinations.


Subject(s)
Breast Neoplasms/diagnosis , Diethylstilbestrol/adverse effects , Estrogens, Non-Steroidal/adverse effects , Mass Screening/statistics & numerical data , Prenatal Exposure Delayed Effects , Adult , Cohort Studies , Female , Guideline Adherence , Humans , Middle Aged , Pregnancy , United States
5.
J Low Genit Tract Dis ; 12(2): 111-7, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18369304

ABSTRACT

OBJECTIVE: To estimate whether women exposed in utero to diethylstilbestrol (DES) report receiving more cervical and general physical examinations compared to unexposed women. MATERIALS AND METHODS: 1994 Diethylstilbestrol Adenosis cohort data are used to assess the degree of recommended compliance of cervical screenings found in 3,140 DES-exposed and 826 unexposed women. Participants were enrolled at 4 sites: Houston, Boston, Rochester, and Los Angeles. Logistic regression modeling was used to analyze mailed questionnaire data, which included reported frequency over the preceding 5 years (1990-1994) of Papanicolaou smears and general physical examinations. RESULTS: Diethylstilbestrol-exposed women exceeded the recommended frequency of Papanicolaou smear screenings [adjusted odds ratio (aOR) = 2.15, 95% CI (confidence interval) = 1.60-2.88] compared to the unexposed. This association held among those without a history of cervical intraepithelial neoplasia (aOR = 1.88, 95% CI = 1.35-2.62). Diethylstilbestrol-exposed women exceeded annual recommendations for physical examinations (aOR = 2.27, 95% CI = 1.16-4.43) among women without a history of chronic disease when compared to unexposed women. CONCLUSIONS: Most DES-exposed women are receiving cervical cancer screening at least at recommended intervals, but one third of the women are not receiving annual Papanicolaou smear examinations.


Subject(s)
Adenocarcinoma/diagnosis , Behavior , Diethylstilbestrol/adverse effects , Papanicolaou Test , Physical Examination/psychology , Uterine Cervical Neoplasms/diagnosis , Vaginal Neoplasms/diagnosis , Vaginal Smears/psychology , Adenocarcinoma/etiology , Administration, Intravaginal , Adult , Diethylstilbestrol/administration & dosage , Estrogens, Non-Steroidal/administration & dosage , Estrogens, Non-Steroidal/adverse effects , Female , Follow-Up Studies , Humans , Middle Aged , Patient Compliance , Physical Examination/methods , Physician-Patient Relations/ethics , Retrospective Studies , Risk Factors , Surveys and Questionnaires , Uterine Cervical Neoplasms/chemically induced , Vaginal Neoplasms/etiology , Vaginal Smears/methods
6.
Am J Epidemiol ; 167(6): 727-33, 2008 Mar 15.
Article in English | MEDLINE | ID: mdl-18192675

ABSTRACT

Menopause onset, on average, occurs earlier among women who smoke cigarettes than among women who do not smoke. Prenatal smoke exposure may also influence age at menopause through possible effects on follicle production in utero. Smoking information was obtained from the mothers of 4,025 participants in the National Cooperative Diethylstilbestrol Adenosis (DESAD) Project, a US study begun in 1975 to examine the health effects of prenatal diethylstilbestrol exposure. Between 1994 and 2001, participants provided information on menopausal status. Cox proportional hazards modeling compared the probability of menopause among participants who were and were not prenatally exposed to maternal cigarette smoke. Participants prenatally exposed to maternal cigarette smoke were more likely than those unexposed to be postmenopause (hazard ratio = 1.21, 95% confidence interval: 1.02, 1.43). The association was present among only those participants who themselves had never smoked cigarettes (hazard ratio = 1.38, 95% confidence interval: 1.10, 1.74) and was absent among active smokers (hazard ratio = 1.03, 95% confidence interval: 0.81, 1.31). In this cohort of participants predominantly exposed to diethylstilbestrol, results suggest that prenatal exposure to maternal cigarette smoke may play a role in programming age at menopause. The possibility that active cigarette smoking modifies this effect is also suggested.


Subject(s)
Attitude to Health , Diethylstilbestrol/toxicity , Environmental Exposure/adverse effects , Maternal Exposure , Maternal Welfare , Menopause , Smoking/adverse effects , Tobacco Smoke Pollution/adverse effects , Adolescent , Adult , Age Factors , Female , Humans , Middle Aged , Pregnancy , Prenatal Exposure Delayed Effects , Risk Assessment , Risk-Taking
7.
Environ Health Perspect ; 115(9): 1314-9, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17805421

ABSTRACT

BACKGROUND: Diethylstilbestrol (DES), a synthetic estrogen widely prescribed to pregnant women during the mid-1900s, is a potent endocrine disruptor. Previous studies have suggested an association between endocrine-disrupting compounds and secondary sex ratio. METHODS: Data were provided by women participating in the National Cancer Institute (NCI) DES Combined Cohort Study. We used generalized estimating equations to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for the relation of in utero DES exposure to sex ratio (proportion of male births). Models were adjusted for maternal age, child's birth year, parity, and cohort, and accounted for clustering among women with multiple pregnancies. RESULTS: The OR for having a male birth comparing DES-exposed to unexposed women was 1.05 (95% CI, 0.95-1.17). For exposed women with complete data on cumulative DES dose and timing (33%), those first exposed to DES earlier in gestation and to higher doses had the highest odds of having a male birth. The ORs were 0.91 (95% C, 0.65-1.27) for first exposure at > or = 13 weeks gestation to < 5 g DES; 0.95 (95% CI, 0.71-1.27) for first exposure at > or = 13 weeks to > or = 5 g; 1.16 (95% CI, 0.96-1.41) for first exposure at < 13 weeks to < 5 g; and 1.24 (95% CI, 1.04-1.48) for first exposure at < 13 weeks to > or = 5 g compared with no exposure. Results did not vary appreciably by maternal age, parity, cohort, or infertility history. CONCLUSIONS: Overall, no association was observed between in utero DES exposure and secondary sex ratio, but a significant increase in the proportion of male births was found among women first exposed to DES earlier in gestation and to a higher cumulative dose.


Subject(s)
Diethylstilbestrol/toxicity , Endocrine Disruptors/toxicity , Estrogens, Non-Steroidal/toxicity , Sex Ratio , Adult , Female , Humans , Infant, Newborn , Male , Maternal-Fetal Exchange , Pregnancy
9.
Breast Cancer Res ; 9(3): R29, 2007.
Article in English | MEDLINE | ID: mdl-17501995

ABSTRACT

INTRODUCTION: Prenatal levels of mitogens may influence the lifetime breast cancer risk by driving stem cell proliferation and increasing the number of target cells, and thereby increasing the chance of mutation events that initiate oncogenesis. We examined in umbilical cord blood the correlation of potential breast epithelial mitogens, including hormones and growth factors, with hematopoietic stem cell concentrations serving as surrogates of overall stem cell potential. METHODS: We analyzed cord blood samples from 289 deliveries. Levels of hormones and growth factors were correlated with concentrations of stem cell and progenitor populations (CD34+ cells, CD34+CD38- cells, CD34+c-kit+ cells, and granulocyte-macrophage colony-forming units). Changes in stem cell concentration associated with each standard deviation change in mitogens and the associated 95% confidence intervals were calculated from multiple regression analysis. RESULTS: Cord blood plasma levels of insulin-like growth factor-1 (IGF-1) were strongly correlated with all the hematopoietic stem and progenitor concentrations examined (one standard-deviation increase in IGF-1 being associated with a 15-19% increase in stem/progenitor concentrations, all P < 0.02). Estriol and insulin-like growth factor binding protein-3 levels were positively and significantly correlated with some of these cell populations. Sex hormone-binding globulin levels were negatively correlated with these stem/progenitor pools. These relationships were stronger in Caucasians and Hispanics and were weaker or not present in Asian-Americans and African-Americans. CONCLUSION: Our data support the concept that in utero mitogens may drive the expansion of stem cell populations. The correlations with IGF-1 and estrogen are noteworthy, as both are crucial for mammary gland development.


Subject(s)
Breast Neoplasms/embryology , Fetal Blood/chemistry , Growth Substances/blood , Hematopoietic Stem Cells/cytology , Hormones/blood , Antigens, CD/analysis , Breast Neoplasms/epidemiology , Cell Division , Erythroid Precursor Cells/cytology , Erythroid Precursor Cells/physiology , Female , Fetal Blood/cytology , Hematopoietic Stem Cells/immunology , Humans , Infant, Newborn , Insulin-Like Growth Factor I/analysis , Pregnancy
10.
CA Cancer J Clin ; 57(1): 7-28, 2007.
Article in English | MEDLINE | ID: mdl-17237032

ABSTRACT

The American Cancer Society (ACS) has developed guidelines for the use of the prophylactic human papillomavirus (HPV) vaccine for the prevention of cervical intraepithelial neoplasia and cervical cancer. These recommendations are based on a formal review of the available evidence. They address the use of prophylactic HPV vaccines, including who should be vaccinated and at what age, as well as a summary of policy and implementation issues. Implications for screening are also discussed.


Subject(s)
Immunization Programs/standards , Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/therapeutic use , Practice Guidelines as Topic , Precancerous Conditions/prevention & control , Preventive Medicine/standards , Uterine Cervical Neoplasms/prevention & control , American Cancer Society , Female , Humans , Male , Papillomavirus Infections/pathology , Precancerous Conditions/pathology , Precancerous Conditions/virology , United States , Uterine Cervical Neoplasms/virology
11.
Am J Epidemiol ; 164(7): 682-8, 2006 Oct 01.
Article in English | MEDLINE | ID: mdl-16887893

ABSTRACT

Age at natural menopause is related to several health outcomes, including cardiovascular disease and overall mortality. Age at menopause may be influenced by the number of follicles formed during gestation, suggesting that prenatal factors could influence menopausal age. Diethylstilbestrol (DES), a nonsteroidal estrogen widely prescribed during the 1950s and 1960s, is related to reproductive tract abnormalities, infertility, and vaginal cancer in prenatally exposed daughters but has not been studied in relation to age at menopause. The authors used survival analyses to estimate the risk of natural menopause in 4,210 DES-exposed versus 1,829 unexposed US women based on responses to questionnaires mailed in 1994, 1997, and 2001. DES-exposed women were 50% more likely to experience natural menopause at any given age (hazard ratio = 1.49, 95% confidence interval: 1.28, 1.74). Among women for whom dose information was complete, there were dose-response effects, with a greater than twofold risk for those exposed to >10,000 mg. The causal mechanism for earlier menopause may be related to a smaller follicle pool, more rapid follicle depletion, or changes in hormone synthesis and metabolism in DES-exposed daughters. Age at menopause has been related, albeit inconsistently, to several exposures, but, to the authors' knowledge, this is the first study to suggest that a prenatal exposure may influence reproductive lifespan.


Subject(s)
Diethylstilbestrol/adverse effects , Estrogens, Non-Steroidal/adverse effects , Menopause/drug effects , Prenatal Exposure Delayed Effects , Age Factors , Female , Humans , Longitudinal Studies , Middle Aged , Pregnancy , Prospective Studies , Surveys and Questionnaires , United States
12.
Cancer Epidemiol Biomarkers Prev ; 15(8): 1509-14, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16896041

ABSTRACT

It has been hypothesized that breast cancer risk is influenced by prenatal hormone levels. Diethylstilbestrol (DES), a synthetic estrogen, was widely used by pregnant women in the 1950s and 1960s. Women who took the drug have an increased risk of breast cancer, but whether risk is also increased in the daughters who were exposed in utero is less clear. We assessed the relation of prenatal DES exposure to risk of breast cancer in a cohort of DES-exposed and unexposed women followed since the 1970s by mailed questionnaires. Eighty percent of both exposed and unexposed women completed the most recent questionnaire. Self-reports of breast cancer were confirmed by pathology reports. Cox proportional hazards regression was used to compute incidence rate ratios (IRR) for prenatal DES exposure relative to no exposure. During follow-up, 102 incident cases of invasive breast cancer occurred, with 76 among DES-exposed women (98,591 person-years) and 26 among unexposed women (35,046 person-years). The overall age-adjusted IRR was 1.40 [95% confidence interval (95% CI), 0.89-2.22]. For breast cancer occurring at ages >or=40 years, the IRR was 1.91 (95% CI, 1.09-3.33) and for cancers occurring at ages >or=50 years, it was 3.00 (95% CI, 1.01-8.98). Control for calendar year, parity, age at first birth, and other factors did not alter the results. These results, from the first prospective study on the subject, suggest that women with prenatal exposure to DES have an increased risk of breast cancer after age 40 years. The findings support the hypothesis that prenatal hormone levels influence breast cancer risk.


Subject(s)
Breast Neoplasms/chemically induced , Carcinogens , Diethylstilbestrol/adverse effects , Prenatal Exposure Delayed Effects , Adult , Cohort Studies , Female , Follow-Up Studies , Humans , Incidence , Middle Aged , Pregnancy , Risk Factors , Surveys and Questionnaires
15.
Epidemiology ; 16(4): 583-6, 2005 Jul.
Article in English | MEDLINE | ID: mdl-15951681

ABSTRACT

BACKGROUND: Diethylstilbestrol (DES) is a synthetic estrogen that was widely prescribed to pregnant women before 1971. DES increases the risk of breast cancer in women who took the drug and the risk of reproductive tract abnormalities in their offspring. Dutch investigators have reported a 20-fold increase in risk of hypospadias among sons of women who were exposed to DES in utero. We assessed this relation in data from an ongoing study of DES-exposed persons. METHODS: Several U.S. cohorts of women with documented exposure in utero to DES have been followed by mailed questionnaires since the 1970s. Comparison subjects are unexposed women of the same ages. In 1997, participants were asked about congenital abnormalities in their children. We calculated prevalence odds ratios for the risk of hypospadias in sons of exposed mothers relative to sons of unexposed mothers using generalized estimating equations to adjust for multiple sons per mother and controlling for maternal age at the son's birth. RESULTS: We obtained data from 3916 exposed and 1746 unexposed women. These women reported a total of 13 liveborn sons with hypospadias (10 exposed, 3 unexposed). The prevalence odds ratio for risk of hypospadias among the exposed was 1.7 (95% confidence interval = 0.4-6.8). CONCLUSIONS: Our findings do not support a greatly increased risk of hypospadias among the sons of women exposed to DES in utero, as has been previously reported.


Subject(s)
Diethylstilbestrol/toxicity , Estrogens, Non-Steroidal/toxicity , Hypospadias/chemically induced , Maternal Exposure/adverse effects , Prenatal Exposure Delayed Effects/chemically induced , Female , Follow-Up Studies , Humans , Hypospadias/epidemiology , Male , Nuclear Family , Odds Ratio , Pregnancy , Prenatal Exposure Delayed Effects/epidemiology , Surveys and Questionnaires , United States/epidemiology
16.
Epidemiology ; 16(3): 342-5, 2005 May.
Article in English | MEDLINE | ID: mdl-15824550

ABSTRACT

BACKGROUND: Clinical studies show that maternal cigarette smoking reduces pregnancy estrogen levels. Women prenatally exposed to maternal cigarette smoke may, therefore, have a lower breast cancer risk because the fetal mammary gland's exposure to maternal estrogen is decreased. Associations between prenatal maternal cigarette smoke exposure and breast cancer, however, have not been observed in previous case-control studies that relied on exposure assessment after the onset of cancer. At the start of this study, cigarette smoking history was obtained directly from the mother. METHODS: The National Cooperative DES Adenosis project was a follow-up study of health outcomes in women prenatally exposed to diethylstilbestrol (DES). At the start of the study, women's mothers provided information about cigarette smoking habits during the time they were pregnant with the study participant. In the current study, the breast cancer rates are compared among 4031 women who were or were not prenatally exposed to maternal cigarette smoke. The resultant relative rate (RR) is adjusted for potential confounding by other breast cancer risk factors using Poisson regression modeling. RESULTS: Fetal exposure to maternal cigarette smoke appeared to be inversely associated with breast cancer incidence (RR = 0.49; 95% confidence interval [CI] = 0.24-1.03). The inverse association was more apparent among women whose mothers smoked 15 cigarettes or fewer per day than among daughters of heavier smokers. There were, however, too few cases to precisely estimate a possible dose-response relationship. CONCLUSION: These results support the hypothesis that in utero exposure to maternal cigarette smoke reduces breast cancer incidence.


Subject(s)
Breast Neoplasms/prevention & control , Maternal-Fetal Exchange , Smoking , Adult , Breast Neoplasms/epidemiology , Female , Humans , Incidence , Pregnancy , United States/epidemiology
17.
Obstet Gynecol ; 105(1): 167-73, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15625159

ABSTRACT

OBJECTIVE: To investigate the association between prenatal diethylstilbestrol (DES) exposure and risk of benign gynecologic tumors. METHODS: We conducted a collaborative follow-up study of women with and without documented intrauterine exposure to DES. We compared the incidence of self-reported ovarian cysts, paraovarian cysts, and uterine leiomyomata confirmed by medical record in DES-exposed and unexposed women. RESULTS: A total of 85 cases of uterine leiomyomata and 168 cases of ovarian or paraovarian cysts were confirmed histologically. After adjustment for age, no association was found between prenatal DES exposure and ovarian cysts or uterine leiomyomata. Prenatal DES exposure was positively associated with paraovarian cysts. CONCLUSION: The present results do not support the hypothesis that prenatal DES exposure increases risk of uterine leiomyomata or ovarian cysts. Prenatal DES exposure was associated with an increased risk of paraovarian cysts, but detection bias cannot be ruled out as an explanation of this finding.


Subject(s)
Diethylstilbestrol/adverse effects , Estrogens, Non-Steroidal/adverse effects , Ovarian Neoplasms/chemically induced , Prenatal Exposure Delayed Effects , Uterine Neoplasms/chemically induced , Adolescent , Adult , Child , Female , Follow-Up Studies , Humans , Leiomyoma/chemically induced , Middle Aged , Ovarian Cysts/chemically induced , Pregnancy , Risk Factors
19.
Obstet Gynecol ; 103(2): 304-9, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14754700

ABSTRACT

Human papillomavirus (HPV) DNA testing was recently approved by the Food and Drug Administration for use as an adjunct to cytology for cervical cancer screening. To help provide guidance to clinicians and patients when using HPV DNA testing as an adjunct to cervical cytology for screening, a workshop was cosponsored by the National Institutes of Health-National Cancer Institute, American Society of Colposcopy and Cervical Pathology (ASCCP), and American Cancer Society. Consensus was reached based on a literature review, expert opinion, and unpublished results from large ongoing screening studies. The conclusions of the workshop were that HPV DNA testing may be added to cervical cytology for screening in women aged 30 years or more. Women whose results are negative by both HPV DNA testing and cytology should not be rescreened before 3 years. Women whose results are negative by cytology, but are high-risk HPV DNA positive, are at a relatively low risk of having high-grade cervical neoplasia, and colposcopy should not be performed routinely in this setting. Instead, HPV DNA testing along with cervical cytology should be repeated in these women at 6 to 12 months. If test results of either are abnormal, colposcopy should then be performed. This guidance should assist clinicians in utilizing HPV DNA testing in an effective manner, while minimizing unnecessary evaluations and treatments.


Subject(s)
DNA Probes, HPV , Mass Screening/methods , Papillomaviridae/isolation & purification , Papillomavirus Infections/diagnosis , Uterine Cervical Dysplasia/pathology , Adult , Aged , Biopsy, Needle , Colposcopy , Cytodiagnosis/methods , DNA, Viral/analysis , Female , Humans , Middle Aged , Sensitivity and Specificity , United States , Vaginal Smears
20.
Obstet Gynecol ; 102(2): 259-65, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12907097

ABSTRACT

OBJECTIVE: To estimate the current cervical cytology screening practices of American College of Obstetricians and Gynecologists (ACOG) Fellows, to establish a baseline for tracking future changes in practice. METHODS: Questionnaires were mailed to a random sample of ACOG Fellows (n = 599) and to a group of Fellows who have regularly participated in past ACOG surveys (n = 409). The questionnaires asked about current cytology screening and evaluation practices and presented clinical practice vignettes with additional questions. Descriptive statistical methods were used to evaluate the responses. RESULTS: Questionnaires were returned by 651 physicians (64.6%); 624 were complete. More than 94% of the respondents start cytology testing at age 18 years. Almost three fourths (74.2%) continue screening indefinitely. More than 80% use a liquid-based method of collection. Almost two thirds (65.1%) order human papillomavirus testing occasionally, usually (81.9%) for reports of atypical squamous cells of undetermined significance (ASCUS). Most Fellows in the sample perform colposcopy for an ASCUS result. Reports of atypical glandular cells resulted in variable approaches to further evaluation. Patient age and history were important variables for all test reports. Legal concerns were mentioned as important determinants of practice patterns. CONCLUSION: In this sample of ACOG Fellows, most perform cervical cytology and evaluate abnormal results in accord with guidelines in place before the recommended changes in screening and evaluation were published in 2003.


Subject(s)
Practice Patterns, Physicians' , Vaginal Smears/statistics & numerical data , Adult , Colposcopy , Female , Gynecology , Humans , Male , Obstetrics , Practice Guidelines as Topic , Vaginal Smears/standards
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