scholarly journals Sleep and circadian disruption and incident breast cancer risk: An evidence-based and theoretical review

2018 ◽  
Vol 84 ◽  
pp. 35-48 ◽  
Author(s):  
Laura B. Samuelsson ◽  
Dana H. Bovbjerg ◽  
Kathryn A. Roecklein ◽  
Martica H. Hall
2015 ◽  
Author(s):  
Vicki Hart ◽  
Susan Sturgeon ◽  
Nicholas Reich ◽  
Lynnette Leidy Sievert ◽  
Sybil Crawford ◽  
...  

2018 ◽  
Vol 36 (15_suppl) ◽  
pp. e24331-e24331
Author(s):  
Kang Liu ◽  
Dingli Song ◽  
Shuai Lin ◽  
Meng Wang ◽  
Tian Tian ◽  
...  

2020 ◽  
Vol 79 (5) ◽  
pp. 581-586 ◽  
Author(s):  
Hjalmar Wadström ◽  
Andreas Pettersson ◽  
Karin E Smedby ◽  
Johan Askling

ObjectivesTo examine the risk of incident breast cancer in women with rheumatoid arthritis (RA), and the risk of RA in women with a history of breast cancer, taking antihormonal treatment for breast cancer into account.MethodsUsing nationwide Swedish registers, women with new-onset RA diagnosed in 2006–2016 were identified and analysed using a cohort and a case–control design. Each patient with RA was matched on age, sex and place of residence to five randomly selected subjects from the general population. Through register linkages, we collected information on breast cancer, breast cancer risk factors (reproductive history and hormone replacement therapy) and socio-economy. The relative risk of breast cancer after RA was assessed using Cox regression, and the relative risk of RA in women with a history of breast cancer was assessed using conditional logistic regression.ResultsThe risk of incident breast cancer in women with RA was reduced and the association was not attenuated by adjustment for breast cancer risk factors (HR=0.80, 95% CI 0.68 to 0.93). The risk of RA in women with a history of breast cancer was similarly reduced (OR=0.87, 95% CI 0.79 to 0.95). Women with breast cancer treated with tamoxifen (OR=0.86, 95% CI 0.62 to 1.20) or aromatase inhibitors (OR=0.97, 95% CI 0.69 to 1.37) did not have an increased risk of RA compared with women with breast cancer treated differently.ConclusionsThe decreased occurrence of breast cancer in patients with RA is present already before RA diagnosis; these reduced risks are not readily explained by hormonal risk factors. Adjuvant antihormonal therapy for breast cancer does not seem to increase RA risk.


2018 ◽  
Vol Volume 10 ◽  
pp. 143-151 ◽  
Author(s):  
Kang Liu ◽  
Weining Zhang ◽  
Zhiming Dai ◽  
Meng Wang ◽  
Tian Tian ◽  
...  

2016 ◽  
Vol 27 (11) ◽  
pp. 1333-1340 ◽  
Author(s):  
Vicki Hart ◽  
Susan R. Sturgeon ◽  
Nicholas Reich ◽  
Lynnette Leidy Sievert ◽  
Sybil L. Crawford ◽  
...  

2009 ◽  
Vol 6 (3) ◽  
pp. 160-166 ◽  
Author(s):  
Allyson Delaune ◽  
Kandace Landreneau ◽  
Katie Hire ◽  
Brenda Dillard ◽  
Melissa Cox ◽  
...  

2017 ◽  
Vol 187 (4) ◽  
pp. 705-716 ◽  
Author(s):  
Deirdre K Tobias ◽  
Akintunde O Akinkuolie ◽  
Paulette D Chandler ◽  
Patrick R Lawler ◽  
JoAnn E Manson ◽  
...  

2015 ◽  
Vol 33 (24) ◽  
pp. 2632-2638 ◽  
Author(s):  
Olle Melander ◽  
Marju Orho-Melander ◽  
Jonas Manjer ◽  
Thomas Svensson ◽  
Peter Almgren ◽  
...  

Purpose In experimental studies, enkephalins (ENKs) and related opioids have been implicated as negative regulators of breast cancer development by enhancing immune-mediated tumoral defense as well as directly inhibiting cancer cells. We hypothesized that plasma levels of ENKs are predictive of the long-term breast cancer risk. Therefore, our objective was to measure pro-ENK A, a surrogate for mature ENK, and evaluate its predictive value for the development of breast cancer in a large population of middle-aged women and an independent study population. Patients and Methods We related pro-ENK in fasting plasma samples from 1,929 healthy women (mean age, 57.6 ± 5.9 years) of the Malmö Diet and Cancer study to breast cancer incidence (n = 123) during a median follow-up of 14.7 years. For replication, pro-ENK was related to risk of breast cancer (n = 130) in an older independent sample from the Malmö Preventive Project consisting of 1,569 women (mean age, 70.0 ± 4.4 years). Results In the Malmö Diet and Cancer study, pro-ENK was inversely related to the risk of incident breast cancer, with a hazard ratio per each standard deviation increment of logarithm-transformed pro-ENK of 0.72 (95% CI, 0.62 to 0.85; P < .001). The linear elevation of risk over pro-ENK quartiles 3, 2, and 1, with the fourth quartile as a reference, was 1.38 (95% CI, 0.73 to 2.64), 2.29 (95% CI, 1.26 to 4.15), and 3.16 (95% CI, 1.78 to 5.60; for the trend, P < .001), respectively. These results were replicated in the Malmö Preventive Project, where the continuous odds ratio for incident breast cancer was 0.63 (95% CI, 0.52 to 0.76; P < .001) and the risk over pro-ENK quartiles 3, 2, and 1, where the fourth quartile was the reference, was 2.48 (95% CI, 1.25 to 4.94), 2.94 (95% CI, 1.50 to 5.77), and 4.81 (95% CI, 2.52 to 9.18; for the trend, P < .001), respecitvely. Conclusion Low fasting plasma concentration of the opioid precursor peptide pro-ENK is associated with an increased risk of future breast cancer in middle-aged and postmenopausal women.


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