Association between long-term use of calcium channel blockers (CCB) and the risk of breast cancer: a retrospective longitudinal observational study protocol

被引:0
作者
Ho, Chau [1 ]
Ha, Ninh Thi [1 ]
Youens, David [1 ,2 ]
Abhayaratna, Walter P. [3 ,4 ]
Bulsara, Max K. [5 ]
Hughes, Jeffery David [6 ,7 ]
Mishra, Gita [8 ]
Pearson, Sallie-Anne [9 ,10 ]
Preen, David B. [10 ,11 ]
Reid, Christopher M. [1 ]
Ruiter, Rikje [12 ,13 ]
Saunders, Christobel M. [14 ,15 ,16 ]
Stricker, Bruno H. [12 ]
van Rooij, Frank J. A. [12 ]
Wright, Cameron [1 ,14 ,17 ,18 ]
Moorin, Rachael [1 ,11 ]
机构
[1] Curtin Univ, Fac Hlth Sci, Sch Populat Hlth, Perth, WA, Australia
[2] Univ Western Australia, Cardiovasc Epidemiol Res Ctr, Sch Populat & Global Hlth, Perth, WA, Australia
[3] Canberra Hlth Serv, Canberra, ACT, Australia
[4] Australian Natl Univ, Sch Med & Psychol, Canberra, ACT, Australia
[5] Univ Notre Dame Australia, Inst Hlth Res, Fremantle, WA, Australia
[6] Curtin Univ, Curtin Med Sch, Perth, WA, Australia
[7] EnergyLab, Sydney, NSW, Australia
[8] Univ Queensland, Sch Publ Hlth, St Lucia, Qld, Australia
[9] Univ New South Wales, Sch Populat Hlth, Sydney, NSW, Australia
[10] NHMRC Med Intelligence Ctr Res Excellence, Sydney, NSW, Australia
[11] Univ Western Australia, Sch Populat & Global Hlth, Perth, WA, Australia
[12] Erasmus MC Univ Med Ctr, Dept Epidemiol, Rotterdam, Zuid holland, Netherlands
[13] Maasstad Hosp, Dept Internal Med, Rotterdam, Zuid holland, Netherlands
[14] Univ Western Australia, Med Sch, Perth, WA, Australia
[15] Univ Melbourne, Melbourne Med Sch, Melbourne, Vic, Australia
[16] Royal Melbourne Hosp, Melbourne, Vic, Australia
[17] Fiona Stanley Hosp, Perth, WA, Australia
[18] Univ Tasmania, Sch Med, Hobart, Tas, Australia
来源
BMJ OPEN | 2024年 / 14卷 / 03期
关键词
Breast tumours; Hypertension; EPIDEMIOLOGY; CLINICAL-PRACTICE; APOPTOSIS; DISEASE; POPULATION; GUIDELINES; MODELS;
D O I
10.1136/bmjopen-2023-080982
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Calcium channel blockers (CCB), a commonly prescribed antihypertensive (AHT) medicine, may be associated with increased risk of breast cancer. The proposed study aims to examine whether long-term CCB use is associated with the development of breast cancer and to characterise the dose-response nature of any identified association, to inform future hypertension management.Methods and analysis The study will use data from 2 of Australia's largest cohort studies; the Australian Longitudinal Study on Women's Health, and the 45 and Up Study, combined with the Rotterdam Study. Eligible women will be those with diagnosed hypertension, no history of breast cancer and no prior CCB use at start of follow-up (2004-2009). Cumulative dose-duration exposure to CCB and other AHT medicines will be captured at the earliest date of: the outcome (a diagnosis of invasive breast cancer); a competing risk event (eg, bilateral mastectomy without a diagnosis of breast cancer, death prior to any diagnosis of breast cancer) or end of follow-up (censoring event). Fine and Gray competing risks regression will be used to assess the association between CCB use and development of breast cancer using a generalised propensity score to adjust for baseline covariates. Time-varying covariates related to interaction with health services will also be included in the model. Data will be harmonised across cohorts to achieve identical protocols and a two-step random effects individual patient-level meta-analysis will be used.Ethics and dissemination Ethical approval was obtained from the following Human research Ethics Committees: Curtin University (ref No. HRE2022-0335), NSW Population and Health Services Research Ethics Committee (2022/ETH01392/2022.31), ACT Research Ethics and Governance Office approval under National Mutual Acceptance for multijurisdictional data linkage research (2022.STE.00208). Results of the proposed study will be published in high-impact journals and presented at key scientific meetings.Trial registration number NCT05972785.
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页数:14
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共 65 条
  • [1] Nifedipine Treatment Reduces Resting Calcium Concentration, Oxidative and Apoptotic Gene Expression, and Improves Muscle Function in Dystrophic mdx Mice
    Altamirano, Francisco
    Valladares, Denisse
    Henriquez-Olguin, Carlos
    Casas, Mariana
    Lopez, Jose R.
    Allen, Paul D.
    Jaimovich, Enrique
    [J]. PLOS ONE, 2013, 8 (12):
  • [2] [Anonymous], 2016, Guideline for the diagnosis and management of hypertension in adults 2016
  • [3] [Anonymous], 2012, GUIDELINES MANAGEMEN
  • [4] Operationalization and validation of a novel method to calculate adherence to polypharmacy with refill data from the Australian pharmaceutical benefits scheme (PBS) database
    Arnet, Isabelle
    Greenland, Melanie
    Knuiman, Matthew W.
    Rankin, Jamie M.
    Hung, Joe
    Nedkoff, Lee
    Briffa, Tom G.
    Sanfilippo, Frank M.
    [J]. CLINICAL EPIDEMIOLOGY, 2018, 10 : 181 - 194
  • [5] Current and future burden of breast cancer: Global statistics for 2020 and 2040
    Arnold, Melina
    Morgan, Eileen
    Rumgay, Harriet
    Mafra, Allini
    Singh, Deependra
    Laversanne, Mathieu
    Vignat, Jerome
    Gralow, Julie R.
    Cardoso, Fatima
    Siesling, Sabine
    Soerjomataram, Isabelle
    [J]. BREAST, 2022, 66 : 15 - 23
  • [6] Long-term use of antihypertensive drugs and risk of cancer
    Assimes, Themistocles L.
    Elstein, Eleanor
    Langleben, Adrian
    Suissa, Samy
    [J]. PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2008, 17 (11) : 1039 - 1049
  • [7] Atkinson JAM, 2015, PUBLIC HEALTH RES PR, V25, DOI 10.17061/phrp2531531
  • [8] Australian Longitudinal Study on Women's Health, 2023, Current HREC approvals for ALSWH data linkage
  • [9] In defense of pharmacoepidemiology - Embracing the yin and yan of drug research
    Avorn, Jerry
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (22) : 2219 - 2221
  • [10] Methods for evidence synthesis in the case of very few studies
    Bender, Ralf
    Friede, Tim
    Koch, Armin
    Kuss, Oliver
    Schlattmann, Peter
    Schwarzer, Guido
    Skipka, Guido
    [J]. RESEARCH SYNTHESIS METHODS, 2018, 9 (03) : 382 - 392