Open Access Study protocol

California Men's Health Study (CMHS): a multiethnic cohort in a managed care setting

Shelley M Enger1, Stephen K Van Den Eeden2*, Barbara Sternfeld2, Ronald K Loo3, Charles P Quesenberry2, Sarah Rowell2, Marianne C Sadler2, Donna M Schaffer24, Laurel A Habel2 and Bette J Caan2

Author Affiliations

1 Department of Research & Evaluation, Kaiser Permanente Medical Care Program, Pasadena, CA 91188, USA

2 Division of Research, Kaiser Permanente Medical Care Program, Oakland, CA 94612, USA

3 Department of Urology, Kaiser Permanente Medical Care Program, Bellflower Medical Center, Bellflower, CA 90706, USA

4 Current at Kaiser Permanente Care Management Institute, Oakland, CA 94612, USA

For all author emails, please log on.

BMC Public Health 2006, 6:172  doi:10.1186/1471-2458-6-172

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2458/6/172


Received:26 January 2006
Accepted:30 June 2006
Published:30 June 2006

© 2006 Enger et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

We established a male, multiethnic cohort primarily to study prostate cancer etiology and secondarily to study the etiologies of other cancer and non-cancer conditions.

Methods/Design

Eligible participants were 45-to-69 year old males who were members of a large, prepaid health plan in California. Participants completed two surveys on-line or on paper in 2002 – 2003. Survey content included demographics; family, medical, and cancer screening history; sexuality and sexual development; lifestyle (diet, physical activity, and smoking); prescription and non-prescription drugs; and herbal supplements. We linked study data with clinical data, including laboratory, hospitalization, and cancer data, from electronic health plan files.

We recruited 84,170 participants, approximately 40% from minority populations and over 5,000 who identified themselves as other than heterosexual. We observed a wide range of education (53% completed less than college) and income. PSA testing rates (75% overall) were highest among black participants. Body mass index (BMI) (median 27.2) was highest for blacks and Latinos and lowest for Asians, and showed 80.6% agreement with BMI from clinical data sources. The sensitivity and specificity can be assessed by comparing self-reported data, such as PSA testing, diabetes, and history of cancer, to health plan data. We anticipate that nearly 1,500 prostate cancer diagnoses will occur within five years of cohort inception.

Discussion

A wide variety of epidemiologic, health services, and outcomes research utilizing a rich array of electronic, biological, and clinical resources is possible within this multiethnic cohort. The California Men's Health Study and other cohorts nested within comprehensive health delivery systems can make important contributions in the area of men's health.

Background

In 2002 – 2003, we established the California Men's Health Study (CMHS), a multiethnic cohort of 84 170 men ages 45 to 69 years who are members of the northern and southern California regions of Kaiser Permanente, the largest managed care organization in California. The major goal of the study is to improve understanding of the development of prostate cancer due to the huge impact it exerts on morbidity and mortality of American males, especially African-American males [1]. By establishing the cohort within an integrated managed care organization, we have access to rich electronic data sources to supplement clinical data collected by survey and to permit the identification and investigation of other health outcomes including other cancers and other non-cancerous conditions.

We obtained baseline data from the men using a two-stage mailed survey, and we employed unique recruitment techniques to enrich the cohort with non-white men. With this cohort, we plan to build on previous work and investigate novel hypotheses in the broad area of men's health. This paper is to describe the baseline demographic characteristics, health status, and lifestyle behaviors of the cohort, to estimate expected cases of cancer, to evaluate the validity of the self-reported data, and to examine how representative the cohort was to the larger population.

Methods/design

Participant eligibility criteria and identification

Eligible participants included all male California Kaiser Permanente (KP) Health Plan members, aged 45 to 69 years in January 2000, who had been members of the health plan for at least one year at recruitment. We identified potential participants from electronic KP membership files containing each member's birthdate, current address, and membership history. At recruitment, nearly 850,000 health plan members met the eligibility criteria.

The study protocol was reviewed and approved for the protection of human subjects by the Institutional Review Boards of Kaiser Permanente Northern California and Kaiser Permanente Southern California.

Participant recruitment and data collection

We recruited participants beginning in January 2002 and concluding at the end of December 2003 using a two-step process in three mailing waves. In the first step of each mailing wave, we mailed a recruitment letter and a short questionnaire in English/Cantonese to potentially eligible health plan members with Chinese surnames [2,3] or in English/Spanish to all other potentially eligible members. The short questionnaire requested information on the men's race/ethnicity, information not routinely collected by the health plan. In the second step of each mailing wave, we mailed a cover letter and a longer, comprehensive questionnaire to participants who had completed and returned the short questionnaire. The cover letter and questionnaire were in the language in which the participant completed the short questionnaire, and the cover letters accompanying the questionnaires were tailored to the participant's specific race/ethnic group and were signed by a well known athletic (black/African-American) or political (Latino) figure or by one of the study investigators (all others). Members were also offered the option to complete the questionnaires electronically in English on a secure website (NCS Pearson, Inc.).

Recruitment mailings were done in three waves using mailing strategies to enhance recruitment of minority male members. In mailing wave one, we mailed to members residing near KP medical centers serving the highest estimated proportion of African-American men and to members we identified with Chinese [2,3] Spanish surnames [4]. In mailing wave two, we mailed to men either who were listed as minority based on hospitalization information or who resided near additional KP facilities with high minority populations. In mailing wave three, due to limited study funds, remaining potentially eligible members were mailed a recruitment letter inviting them to complete both questionnaires on the website, and they had the option of requesting a paper questionnaire. Mailing waves included 200,000 to 350,000 members.

Questionnaires

The short (2-page) questionnaire included questions on race/ethnicity, anthropometrics, prostate specific antigen (PSA) testing history and personal history of prostate cancer or benign prostatic hyperplasia (BPH).

The longer (24-page) questionnaire solicited information on demographics, family history of cancer, health and lifestyle, prostate-related symptoms and conditions, other existing health conditions, medication/drug use, physical activity, tobacco use, diet/supplement use, country of origin, duration of U.S. residency, income, and sexual development, orientation, and health. Lower urinary tract symptoms were assessed using the American Urology Association Symptom Index (AUASI) [5], while erectile dysfunction was assessed by a four-level single question adapted form the Massachusetts Male Aging Study [6]. We assessed diet with a detailed semi-quantitative food-frequency questionnaire adapted from a questionnaire developed for the Women's Health Initiative and other studies [7-9], modified to men's studies of prostate health [10]. We assessed physical activity with questions adapted from the CARDIA Physical Activity History [11-13] that queried the men about the frequency and duration of their participation in specific types of moderate and vigorous recreational, household, and work-related activities. The CARDIA questionnaire has indirect validity against aerobic capacity and percent body fat [11,12] and a strong inverse relation with most cardiovascular disease risk factors [14,15].

We manually reviewed paper questionnaires for stray marks, completeness, and multiple responses. We optically scanned the questionnaires into study computers using ScanTools® II Software (Pearson NCS, Inc, Bloomington, MN). We uploaded the data into SAS data management databases (SAS Statistical Software Version 8.2, SAS Statistical Institute, Cary, NC) for cleaning and storage. We used computerized edits to assess the data for logic errors, out-of-range values, missing data, and multiple responses.

Analytical/statistical methods

We constructed the variables reported in the tables from both self-reported and health plan data. We linked study databases with electronic health plan databases using the member's health record number, a unique subject identifier. The health plan data provided information about the participants' KP membership history, hospitalization history, laboratory results, and other health conditions including cancer and diabetes. We used health plan data to validate specific survey data items when comparable health plan data existed.

We created new variables and categorical variables from the raw questionnaire data. Body mass index (BMI), a measure of obesity, was calculated as weight (kilograms) divided by the square of height (meters2). Participants who did not complete all pages of the food frequency questionnaire (at least five items per page) or who had total calculated energy intake below (less than 800 kcal) or above (greater than 5,000 kcal) what we considered reasonable were excluded from the nutrient analyses. Recreational physical activity summary scores were derived by multiplying assigned MET values13 by duration and frequency and summing across activities. We defined vigorous activities as participating in a minimum of 1,260 MET-hours per week, on average, equivalent to at least 3.5 hours of activity with a minimum MET level of 6. We defined moderate and vigorous activities combined as participating in a minimum of 630 MET-hours of activity per week, on average, equivalent to at least 3.5 hours of activity with a minimum MET level of 3.

We determined the expected number of cases of prostate, colorectal, lung, and bladder cancer and melanoma based on the expected baseline age distribution of the cohort of 84,170 men, and the age and race/ethnic specific annual (average 1992–1996) cancer incidence rates for the State of California. We account for an assumed 4% annual rate of loss to follow-up, due to mortality and loss to follow-up, based on our experience with other cohort studies.

We calculated percent agreement between BMI derived from self-reported weight and height and BMI from clinical databases. We cross tabulated the data grouped according to BMI categories of normal weight (<25), overweight (25–29), and obese (30 or higher), and then calculated the percent agreement as the total number of participants for whom BMI was classified in the same category by both sources divided by the total number of participants with clinical BMI data available.

Cohort characteristics

Response rates varied across mailing strategies (Table 1). Short questionnaire responses were substantially higher when we mailed questionnaires (waves one and two) than when we invited the men to complete the questionnaire on-line (wave three). Conversely, among those who completed the short questionnaire, the responses to the long questionnaire were 50% higher among men recruited in wave three compared to men recruited in waves one and two. Overall, the participants completed nearly one-quarter of the short questionnaires and nearly one-third of the long questionnaires on the secure website.

Table 1. Recruitment figures: CMHS Cohort, California.

A total of 84170 men joined the cohort, and nearly 40% were minority (Table 2). Participants were distributed fairly evenly across age groups, although Latino, Asian, and 'other/mixed race/ethnicity' men tended to be somewhat younger, a reflection of the general KP membership age distribution. Educational attainment varied by race/ethnicity, with over half of whites and Asians having earned at least a college degree compared to one-third of black participants and over one-fifth of Latinos. Income distributions also varied by race/ethnicity, with white participants reporting the highest and Latinos reporting the lowest incomes.

Table 2. Distribution of participants by age, educational attainment, and current household income, by race/ethnicity: CMHS Cohort, California.

One in five participants had a history of BPH, a benign but frequently symptomatic prostate enlargement (Table 3). Rates among white men were the highest and were more than 50% higher than those of Asian men who experienced the lowest rates. A history of prostatitis, a painful inflammation of the prostate usually due to infection, was also most common among white participants and more than twice as common as among Asians. Nearly half (48.6%) of the cohort reported moderate or severe LUTS, while 29.9% of the men reporting sometimes or never being able to get or keep an erection (e.g., erectile dysfunction).

Table 3. Distribution of specific prostate conditions and laboratory tests, by race/ethnicity: CMHS Cohort, California.

Most participants reported having received PSA testing sometime in the past (Table 3). Black participants were most likely and Latino participants were least likely to have reported receiving a test. We observed only slight race/ethnic variation in the percentage of participants who received fasting glucose, HDL cholesterol, cholesterol panel, or triglyceride laboratory tests within the five years before cohort enrollment. In general, however, Asian participants were most likely and Latino participants were least likely to have received the tests.

We observed that energy and nutrient intakes varied somewhat by race/ethnicity (Table 4). Asian participants reported the lowest consumption of calories and percent calories from fat, fiber, protein and alcohol. Conversely, white participants reported the highest consumption of calories, fiber, and alcohol. Fruit consumption (servings) was similar across race/ethnic groups.

Table 4. Mean daily energy and nutrient intakes, median body size, percentage of participation in moderate and vigorous physical activities, current smoking status, and sexual orientation, by race/ethnicity, based on self-reported survey data: CMHS Cohort, California.

The median BMI for the cohort was high with more than 50% of participants considered overweight (Table 4). Blacks and Latinos had the highest and Asians had the lowest median BMI. Nearly two-thirds of participants reported regular moderate or vigorous recreational activities and over 40% reported regular vigorous recreational activities, with the highest rates among white participants. Although smoking rates were low overall, rates among black participants, the highest, were more than double the rates of Asian participants, the lowest.

Over 5,000 participants identified themselves as other than heterosexual, with the highest proportion among white and the lowest proportion among Asian participants (Table 4).

We anticipate that nearly 1,500 prostate cancer diagnoses will occur among participants during the 5 years after cohort inception (Table 5). We also anticipate sufficient diagnoses of lung and colorectal cancers, and other diseases of similar incidence, within 5 years to conduct well powered analyses of etiological factors. There may also be sufficient bladder cancer and melanoma diagnoses to conduct basic etiological analyses.

Table 5. Expected number of cancer diagnoses by December 31, 2006: CMHS Cohort, California.

In addition to cancer outcomes, a significant number of newly diagnosed cases of cardiovascular diseases and neurodegenerative diseases are expected. Based on estimates in the literature, estimates of the expected number of new cases in the CMHS participants after five years of follow-up (and adjusting for loss of follow-up and mortality) include: 5,000 new cases of myocardial infarction, 5,100 cases of congestive heart failure, 180 cases of Parkinson's disease, 7,000 cases of dementia, and 370 cases of Alzheimer's disease.

We compared CMHS participants with male participants in the California Health Interview Survey (CHIS), a population-based telephone survey of 55,000 California residents in 2001 [16] (Table 6). Distributions of participants were similar for the demographic factors examined as well as for BMI. Substantially more CMHS participants had reported at least one PSA test than CHIS participants, probably due to complete insurance coverage among CMHS participants.

Table 6. Self-reported demographic, body mass index, and prostate cancer screening data in the CMHS Cohort compared to California Health Interview Survey* (CHIS), males aged 50 to 64 years.

We also performed a small comparison of CMHS participants to non-participants of the same age range. A total of 84.4% CMHS participants were KP members for at least five years compared to 75.3% of non-participants. The percentage hospitalized during the 5 years before recruitment were similar for the two groups (17.0% of participants versus 15.6% of non-participants), and the prevalence of diabetes mellitus was nearly identical (13.5% for participants versus 13.6% for non-participants).

We validated BMI calculated from self-reported weight and height in relation to BMI reported in health plan clinical databases (Table 7). Overall, the percentage of participants who were classified into the same BMI categories by both sources was over 80%, and the percent of participants who were classified into the same or adjacent categories was 99.4%.

Table 7. Percent agreement between BMI calculated from self-reported weight and height and from electronic clinical databases: CMHS Cohort1, California.

Discussion

We assembled a large, multiethnic male cohort from the membership of the largest managed care organization in California to study prostate cancer etiology and the etiologies of other cancer and non-cancerous conditions. CMHS participants are diverse in socioeconomic status as well as race/ethnicity, where both ends of the income and education spectrum are well represented in the cohort. The managed care setting is ideal to study disease risk factors and health services delivery where health care access issues are minimized and supplemental data sources are maximized and can be used to verify and extend the questionnaire data.

The availability of supplemental electronic data is a unique and important strength of this cohort. For example, we can conduct electronic data linkages between cohort and electronic health plan files to obtain current and historical data, obtain information on outcomes other than cancer, and conduct validation studies of self-reported data. Electronic data sources can be used to follow the participants for updated contact information from membership files, cancer diagnoses through cancer registry databases, and deaths of through linkage with health plan mortality databases derived from state death certificate files.

Another advantage of these data within this setting is the ability to assess the sensitivity and specificity of the self-reported data on health conditions and PSA testing by comparing these data to clinical databases of the health plan. The BMI from self-report was in high agreement with clinical BMI data, suggesting that data collection by self-report was reliable. However, a limitation of these analyses is the inability to identify diagnoses that pre-dated the participant's health plan membership or the inception date of the electronic database.

Another unique strength of this cohort is the potential to conduct efficient biospecimen-based research studies. The health plan maintains tissue banks of tumor and non-tumor tissue blocks, some from as early at the 1950s, and the health plan manages a system of clinical laboratories that can be used for the efficient collection of blood specimens. The availability of these resources greatly facilitates research of genetic markers and other molecular studies.

Prospective cohort studies are considered the gold standard of epidemiologic research because many biases that can hamper interpretation of case-control studies are, by design, minimized in prospective cohort studies [17,18]. Cohort studies also facilitate the study of multiple outcomes, unlike other observational study designs. A drawback to cohort studies is the long follow-up time often required to obtain sufficient power to conduct statistical analyses, typically low recruitment rates, and loss to follow-up that can harm internal validity. However, we anticipate having sufficient statistical power within five years of cohort inception to conduct prostate cancer analyses. Our cost-saving strategies of not re-contacting men who did not respond initially and of mailing the long questionnaire only to men who completed the 2-page questionnaire enhanced the likelihood of obtaining favorable follow-up rates and therefore high internal study validity, because the final cohort included only the men who were willing to complete two questionnaires separated in time.

The relatively low recruitment rates raise the issue of generalizability of the study findings to the broader community, although this aspect of this study is within the range that is found in other general cohort recruitment efforts. Prospective cohorts are considered valuable partly because well conducted and followed cohorts allow internally valid comparisons to be made [18-21], similar to clinical trials which are considered to be internally valid despite inclusion of typically highly selected participants [22]. No cohort is strictly generalizable to the population as a whole. Rather, research from some of the most widely cited cohorts is derived from study populations that are overwhelmingly from one race/ethnic group [23-30], occupational group or class group [23,24,26,27], or observational studies following clinical trials [31, 32, 33]. Nonetheless, the CMHS cohort was similar to the population of health plan members on important characteristics and appeared similar to men who responded a general health survey in California on a variety of important demographic and clinical characteristics. Thus, a cohort such as this one should be able to address biologically relevant questions related to disease onset and progression.

A wide variety of epidemiologic, health services, and outcomes research is possible within this multiethnic cohort. The cohort is available for study by non-Kaiser Permanente investigators and students conditional upon approval by the CMHS Proposal Review Committee. A rich array of electronic, biological, and clinical resources is available to supplement and enhance the survey data and to facilitate the study of outcomes other than cancer while controlling for major health risk factors. The large prospective cohorts in the United States have made enormous contributions to our knowledge of the causes of cancer and other diseases, and we believe the CMHS is poised to make important contributions in the area of men's health.

Competing interests

The author(s) declare that they have no competing interests.

Authors' contributions

SME was the principal author of the manuscript. SME, BS, SKV, RKL, CPQ, SR, DMS, and BJC made substantial contributions to the conception and design of the study, and to the acquisition of funding. SME, BS, SKV, RKL, CPQ, MCS, LAH and BJC contributed to the analysis of the data. All authors contributed to the interpretation of the data, the drafting of manuscript, and have read and given approval to the final version of the manuscript.

Acknowledgements

This study was supported in part by funds from the California Cancer Research Program, grant number 99-86883, and from The Community Benefit Program, Kaiser Permanente Northern California.

The authors wish to thank the participants of the CMHS for their involvement, and to acknowledge the many contributions to the study by study staff and especially Sharon Wi, Amy Liu, and Adrienne Castillo. The authors also wish to thank the Chiefs of Urology in southern and northern California KP for their support of the study.

References

  1. Society AC: Cancer Facts & Figures, 2004. Atlanta (Publication number 5008-04), American Cancer Society; 2004. OpenURL

  2. Choi BC, Hanley AJ, Holowaty EJ, Dale D: Use of surnames to identify individuals of Chinese ancestry.

    Am J Epidemiol 1993, 138:723-734. PubMed Abstract OpenURL

  3. Hage BH, Oliver RG, Powles JW, Wahlqvist ML: Telephone directory listings of presumptive Chinese surnames: an appropriate sampling frame for a dispersed population with characteristic surnames.

    Epidemiology 1990, 1:405-408. PubMed Abstract OpenURL

  4. Word DL, Perkins RC: Building a Spanish surname list for the 1990's: a new approach to an old problem. Volume Technical Working Paper No. 13. Washington, DC, Population Division, US Bureau of the Census; 1996.

  5. Barry MJ, Fowler FJJ, O'Leary MP, Bruskewitz RC, Holtgrewe HL, Mebust WK, Cockett AT: The American Urological Association symptom index for benign prostatic hyperplasia. The Measurement Committee of the American Urological Association.

    J Urol 1992, 148:1549-1557. PubMed Abstract OpenURL

  6. Derby CA, Araujo AB, Johannes CB, Feldman HA, McKinlay JB: Measurement of erectile dysfunction in population-based studies: the use of a single question self-assessment in the Massachusetts Male Aging Study.

    Int J Impot Res 2000, 12:197-204. PubMed Abstract | Publisher Full Text OpenURL

  7. Kristal AR, Patterson RE, Neuhouser ML, Thornquist M, Neumark-Sztainer D, Rock CL, Berlin MC, Cheskin L, Schreiner PJ: Olestra Postmarketing Surveillance Study: design and baseline results from the sentinel site.

    J Am Diet Assoc 1998, 98:1290-1296. PubMed Abstract | Publisher Full Text OpenURL

  8. Kristal AR, Feng Z, Coates RJ, Oberman A, George V: Associations of race/ethnicity, education, and dietary intervention with the validity and reliability of a food frequency questionnaire: the Women's Health Trial Feasibility Study in Minority Populations.

    Am J Epidemiol 1997, 146:856-869. PubMed Abstract OpenURL

  9. Patterson RE, Kristal AR, Tinker LF, Carter RA, Bolton MP, Agurs-Collins T: Measurement characteristics of the Women's Health Initiative food frequency questionnaire.

    Ann Epidemiol 1999, 9:178-187. PubMed Abstract | Publisher Full Text OpenURL

  10. Kristal AR, Stanford JL, Cohen JH, Wicklund K, Patterson RE: Vitamin and mineral supplement use is associated with reduced risk of prostate cancer.

    Cancer Epidemiol Biomarkers Prev 1999, 8:887-892. PubMed Abstract | Publisher Full Text OpenURL

  11. Jacobs DRJ, Ainsworth BE, Hartman TJ, Leon AS: A simultaneous evaluation of 10 commonly used physical activity questionnaires.

    Med Sci Sports Exerc 1993, 25:81-91. PubMed Abstract OpenURL

  12. Jacobs DRJ, Hahn L, Haskell WL, Pirie P, Sidney S: Validity and reliability of short physical activity history: CARDIA and the Minnesota Heart Health Program.

    Journal of Cardiopulmonary Rehabilitation 1989, 9:448-459. OpenURL

  13. Sidney S, Jacobs DRJ, Haskell WL, Armstrong MA, Dimicco A, Oberman A, Savage PJ, Slattery ML, Sternfeld B, Van Horn L: Comparison of two methods of assessing physical activity in the Coronary Artery Risk Development in Young Adults (CARDIA) Study.

    Am J Epidemiol 1991, 133:1231-1245. PubMed Abstract OpenURL

  14. Schmitz KH, Jacobs DRJ, Leon AS, Schreiner PJ, Sternfeld B: Physical activity and body weight: associations over ten years in the CARDIA study. Coronary Artery Risk Development in Young Adults.

    Int J Obes Relat Metab Disord 2000, 24:1475-1487. PubMed Abstract | Publisher Full Text OpenURL

  15. Ponce NA, Lavarreda SA, Yen W, Brown ER, DiSogra C, Satter DE: The California Health Interview Survey 2001: translation of a major survey for California's multiethnic population.

    Public Health Rep 2004, 119:388-395. PubMed Abstract | Publisher Full Text OpenURL

  16. Breslow NE, Day NE: Statistical Methods in Cancer Research. Volume II - The Design and Analysis of Cohort Studies. Lyon, International Agency for Reseach on Cancer; 1987. OpenURL

  17. Samet JM, Munoz A: Evolution of the cohort study.

    Epidemiol Rev 1998, 20:1-14. PubMed Abstract OpenURL

  18. Greenland S: Response and follow-up bias in cohort studies.

    Am J Epidemiol 1977, 106:184-187. PubMed Abstract OpenURL

  19. Hunt JR, White E: Retaining and tracking cohort study members.

    Epidemiol Rev 1998, 20:57-70. PubMed Abstract OpenURL

  20. Rothman KJ, Greenland S: Precision and validity in epidemiologic studies. In Modern Epidemiology. Volume 8. 2nd edition. Boston, Little, Brown & Co.; 1998::115-134. OpenURL

  21. Meinert CL: Clincial Trials. Design, conduct, and analysis.. New York, NY, Oxford University Press; 1986. OpenURL

  22. Adami HO, Bergstrom R, Engholm G, Nyren O, Wolk A, Ekbom A, Englund A, Baron J: A prospective study of smoking and risk of prostate cancer.

    Int J Cancer 1996, 67:764-768. PubMed Abstract | Publisher Full Text OpenURL

  23. Colditz GA: The nurses' health study: a cohort of US women followed since 1976.

    J Am Med Womens Assoc 1995, 50:40-44. PubMed Abstract OpenURL

  24. Folsom AR, Kaye SA, Potter JD, Prineas RJ: Association of incident carcinoma of the endometrium with body weight and fat distribution in older women: early findings of the Iowa Women's Health Study.

    Cancer Res 1989, 49:6828-6831. PubMed Abstract OpenURL

  25. Giovannucci E, Leitzmann M, Spiegelman D, Rimm EB, Colditz GA, Stampfer MJ, Willett WC: A prospective study of physical activity and prostate cancer in male health professionals.

    Cancer Res 1998, 58:5117-5122. PubMed Abstract OpenURL

  26. Horn-Ross PL, Hoggatt KJ, West DW, Krone MR, Stewart SL, Anton H, Bernstei CL, Deapen D, Peel D, Pinder R, Reynolds P, Ross RK, Wright W, Ziogas A: Recent diet and breast cancer risk: the California Teachers Study (USA).

    Cancer Causes Control 2002, 13:407-415. PubMed Abstract | Publisher Full Text OpenURL

  27. White E, Patterson RE, Kristal AR, Thornquist M, King I, Shattuck AL, Evans I, Satia-Abouta J, Littman AJ, Potter JD: VITamins And Lifestyle cohort study: study design and characteristics of supplement users.

    Am J Epidemiol 2004, 159:83-93. PubMed Abstract | Publisher Full Text OpenURL

  28. Yuan JM, Ross RK, Wang XL, Gao YT, Henderson BE, Yu MC: Morbidity and mortality in relation to cigarette smoking in Shanghai, China. A prospective male cohort study [see comments].

    JAMA 1996, 275:1646-1650. PubMed Abstract | Publisher Full Text OpenURL

  29. Zheng W, Chow WH, Yang G, Jin F, Rothman N, Blair A, Li HL, Wen W, Ji BT, Li Q, Shu XO, Gao YT: The Shanghai Women's Health Study: rationale, study design, and baseline characteristics.

    Am J Epidemiol 2005, 162:1123-1131. PubMed Abstract | Publisher Full Text OpenURL

  30. Gann PH, Ma J, Giovannucci E, Willett W, Sacks FM, Hennekens CH, Stampfer MJ: Lower prostate cancer risk in men with elevated plasma lycopene levels: results of a prospective analysis.

    Cancer Res 1999, 59:1225-1230. PubMed Abstract | Publisher Full Text OpenURL

  31. Hak AE, Stampfer MJ, Campos H, Sesso HD, Gaziano JM, Willett W, Ma J: Plasma carotenoids and tocopherols and risk of myocardial infarction in a low-risk population of US male physicians.

    Circulation 2003, 108:802-807. PubMed Abstract | Publisher Full Text OpenURL

  32. Verhoef P, Hennekens CH, Malinow MR, Kok FJ, Willett WC, Stampfer MJ: A prospective study of plasma homocyst(e)ine and risk of ischemic stroke.

    Stroke 1994, 25:1924-1930. PubMed Abstract OpenURL

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2458/6/172/prepub