Physical activity does not alter prolactin levels in post-menopausal women: results from a dose-response randomized controlled trial
© The Author(s) 2017
Received: 28 December 2016
Accepted: 4 July 2017
Published: 13 July 2017
Increased circulating levels of prolactin have been associated with increased risk of both in situ and invasive breast cancer. We investigated whether or not physical activity had a dose–response effect in lowering plasma levels of prolactin in postmenopausal women.
Four hundred previously inactive but healthy postmenopausal women aged 50–74 years of age were randomized to 150 or 300 min per week of aerobic physical activity in a year-long intervention. Prolactin was measured from fasting samples with a custom-plex multiplex assay.
A high compared to moderate volume of physical activity did not reduce plasma prolactin levels in intention-to-treat (Treatment Effect Ratio (TER) 1.00, 95% Confidence Interval (CI) 0.95 – 1.06) or per-protocol analyses (TER 1.02, 95% CI 0.93 – 1.13).
It is unlikely that changes in prolactin levels mediate the reduced risk of breast cancer development in post-menopausal women associated with increased levels of physical activity.
clinicaltrials.gov identifier: NCT01435005.
KeywordsPhysical Activity Randomized Controlled Trial Breast Cancer Prolactin
The primary hypothesized mechanisms underlying the associations between physical activity and reduced breast cancer include reductions in adiposity, sex hormone levels, insulin resistance and chronic inflammation . These pathways only explain some portion of the association and additional mechanisms require identification and further investigation.
Prolactin is a luteotropic peptide hormone involved in regular lactation which is produced by the anterior pituitary gland. Increased circulating levels of prolactin have been associated with increased risk of both in situ and invasive breast cancer . Two previous exercise intervention trials in post-menopausal women did not observe changes in prolactin levels in response to moderate physical activity [3, 4] compared to controls. As part of the Breast cancer and Exercise Trial in Alberta (BETA) we investigated: 1) the effects of increased levels of moderate to vigorous physical activity (MVPA) on levels of prolactin and 2) whether a higher level of activity led to larger changes in prolactin levels.
Materials and methods
The design of the BETA study has been previously described in detail . Briefly, 400 previously inactive but otherwise healthy postmenopausal women of age were randomized to 150 (MODERATE) or 300 (HIGH) minutes per week of aerobic physical activity for a year-long intervention. Women were eligible for randomization if they were between 50–74 years of age, with no previous diagnosis of invasive cancer, no major comorbidities, obtained physical approval for participation, had a body mass index of 22–40, were moderately sedentary, not a current smoker or excessive drinker, not currently on a weight loss program, English speaking and not planning to be out of the study site areas for more than 4 consecutive weeks during the subsequent 18 months. Both intervention arms were prescribed the same frequency (five days/week) and intensity (moderate-to-vigorous) of aerobic exercise. The training targets were 60 minutes/session (300 total minutes/week) for the HIGH group, and 30 minutes/session (150 total minutes/week) for the MODERATE group. Wrist-worn heart rate were given to each participant and used to ensure a 65–75% maximum heart rate reserve (HRR) was being achieved during each exercise session. A ramp-up period was included where the intensity, frequency and duration of exercise were gradually increased during the first three months of the intervention until the target exercise prescriptions were attained. Fasting blood samples were collected from all participants at baseline, 6 and 12 months following a 24 h abstinence from alcohol intake and exercise and at least 10 h after their last meal. Prolactin levels in plasma were measured with a custom-plex multiplex assay (Eve Technologies, Calgary, AB, Canada), using the Bio-Plex™ 200 system (Bio-Rad Laboratories, Inc., Hercules, CA, USA). The assay sensitivity for prolactin was 30.2 pg/ml and the inter-assay coefficient of variation was 5.5%. Samples for each participant at different time points were all analyzed in the same batch and each batch included an equal number of MODERATE and HIGH blood samples.
Predicted VO2 max was estimated from a modified Balke treadmill test  using the multistage model and the American College of Sports Medicine metabolic equations for estimating maximum oxygen consumption . Body composition was estimated from full body dual energy X-ray absorptiometry (DXA) scans to assess overall percent body fat and total fat mass. Computed tomography (CT) scans were taken at the level of the umbilicus to measure subcutaneous and intra-abdominal adiposity.
We considered the comparison of means of 12-month outcomes (log transformed, with no adjustment for baseline values) for the prolactin outcomes. Standard deviation was estimated from previous reports . A sample size of 200 participants per group provided 90% power to detect anticipated changes of 4% between the treatment groups at α = 0.05. Prolactin changes in the two arms were compared in both intention-to-treat and per-protocol analysis using linear mixed models as previously described, adjusting for baseline prolactin levels . A per-protocol analysis was conducted on participants achieving ≥60% of prescribed exercise duration in their target heart rate zone. To investigate whether the effects of exercise were restricted to particular subgroups, stratified analyses were conducted on a priori variables including baseline body mass index (BMI (weight (kg)/height (m2)), estimated physical fitness (VO2max), and total percent body fat.
The study protocol was approved by the Alberta Cancer Research Ethics Committee and the Conjoint Health Research Ethics Board of the University of Calgary and the Health Research Ethics Board of the University of Alberta. All participants provided written informed consent.
The distribution of the study participants’ baseline characteristics was similar in the two trial arms with no meaningful differences between arms . Baseline prolactin levels were 10565 (SD = 6963) pg/ml in MODERATE group and 10478 (SD = 5150) pg/ml in HIGH group (p = 0.89). Overall, we did not observe statistically significant effects for increasing quartiles of physical activity and change in level of prolactin in the n = 384 women included in the analyses (non-randomized analysis – results not shown).
Intention-to-treat and per-protocol analyses of prolactin concentrations between high and moderate volume exercise groups in BETA, (n = 386)
Ratio of High/Moderateb
8720 – 10064
8467 – 9641
0.95 – 1.06
8713 – 9992
8457 – 9613
8002 – 9591
7904 – 9576
0.93 – 1.13
8284 – 11248
8275 – 10600
Stratified analyses of changes in prolactin between high volume and moderate volume exercise groups in BETA, 2010–2013 (n = 386)
Prescribed exercise duration
6 months percent change from baseline
12 months percent change from baseline
Ratio of HIGH:MOD
Time at high intensityc
0.93 – 1.21
0.88 – 1.17
< 27.2 ml/kg min
≥ 27.2 ml/kg min
Total body fatf
< 29.7 kg
≥ 29.7 kg
Overall, a higher volume of exercise compared to a standard volume did not reduce prolactin levels in BETA. Moreover, the effects did not vary according to exercise adherence or baseline fitness levels, BMI, and total body fat.
This exercise intervention trial is the first study to examine the effects of a high versus moderate volume of MVPA aerobic exercise on prolactin levels in postmenopausal women. Previous studies comparing 12 months of moderate-intensity aerobic exercise to no exercise have reported null effects on prolactin levels [3, 4]. Similarly, the results from these previous trials remained unchanged when exercise adherence, measured as minutes of exercise per day, was considered [3, 4]. In the study by Reding et al. , baseline BMI did not alter the treatment effect. In the study by Tworoger et al. , change in percent body fat did not mediate the intervention effect however, women in the exercise group who increased their VO2 max by >5% had a statistically significant reduction in prolactin levels.
Our analyses were motivated by the strong animal and in vitro data supporting an important role of prolactin in breast carcinogenesis  and epidemiologic data suggesting an association of increased levels with breast cancer risk . While our study did not observe significant impacts of exercise on levels of prolactin, it is worth noting that there are complex relationships between exercise and prolactin levels which may explain our null findings. For example, threshold effects of exercise intensity have been observed in the literature , which suggests that the intensity of exercise in the BETA trial may not have been high enough despite a target >65% HRR. Furthermore, effects may differ by age as there are several studies among young athletic populations where increased levels of prolactin are reported post-acute bouts of exercise [12–14], while effects among older sedentary populations are less well characterized.
In conclusion, the results from the BETA study suggest that 300 min per week of moderate-intensity aerobic exercise does not reduce prolactin levels more than 150 min per week in a year-long intervention in postmenopausal women. It is unlikely that changes in prolactin levels mediate the reduced risk of breast cancer development in post-menopausal women associated with increased physical activity at any level.
Calgary Study Coordinators were: Krista Carlson, Sana Fakih, Megan Farris, Quinn Harris, Sarah MacLaughlin, Erica Roberts, and Kristen Simone. Edmonton Study Coordinators were: Natalie Ilkiw, Ciara Kallal, and Dr. Amy Speed Andrews. Assistance with information sessions was provided in Calgary by Drs. Brigid Lynch and Fabiola Aparicio-Ting. Calgary Exercise Trainers were: Carrie Anderson, Alia Bharwani, Shannon Brown, Ashley Cuthbert, Sue Daniel, Julie Gowans, Margo Graham, Erin Korsbrek, Kathleen Kranenburg, Jessica Morrison, Jason Ng, Nicole Slot, Tania White, and Kaila Wright. Edmonton Exercise Trainers were: Arne Anderson, Lisa Belanger, Jennifer Crawford, Cindy Forbes, Alyssa Hindle, Corey Kuzik, Erin McGowan, Mary Norris, Janel Park, Julianne Symons, Linda Trinh, Stephanie Voaklander and Lynne Wong. Study recruiters were: Jennie Duke, Jasdeep Hayer, Trisha Kelly, Jasmine Lee, and Lilly Mah. Data entry was done by: Sinead Boyle, Barbara Mercer, Carla Quesnel and Trisha Kelly. Data management, including database creation, questionnaire design, data integrity and quality control, was done by: Dr. Steven Szarka, Farit Vakhetov, and Wendy Walroth. Qinggang Wang was responsible for the randomization procedures, sample size calculations and some data verification. The late Dr. Robert C. Millikan was a co-investigator on this trial and contributed to the study design and methods.
This work was supported by a Career Development Award in Prevention (#703917) from the Canadian Cancer Society Research Institute held by Dr. Brenner. Dr. Friedenreich holds a Health Senior Scholar Award from Alberta Innovates-Health Solutions and is the Alberta Cancer Foundation Weekend to End Women’s Cancers Breast Cancer Chair. Dr. Courneya holds a Canada Research Chair in Physical Activity and Cancer.
Availability of data and materials
The datasets generated during and/or analyzed during the current study are not publicly available but are available from the corresponding author on reasonable request.
DB assisted in data collection, interpretation and wrote the manuscript. YR completed the data analysis and assisted in interpretation and writing of the manuscript. AM assisted in interpretation and writing of the manuscript. CF and KC were responsible for the design and conduct of the study, data collection as well as writing and critical review of the manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
This study was approved by the Health Research Ethics Board of Alberta and all participants consented to participate.
Consent for publication
The authors declare that they have no competing interests.
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