Causal relationships between breast cancer risk factors based on mammographic features
Background Mammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk differently and could reveal distinct information about breast cancer risk. We aimed to investigate causal relationships between these intercorrelated mammo...
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Published in: | Breast cancer research : BCR Vol. 25; no. 1; pp. 1 - 127 |
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Abstract | Background Mammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk differently and could reveal distinct information about breast cancer risk. We aimed to investigate causal relationships between these intercorrelated mammogram risk scores to determine their relevance to breast cancer aetiology. Methods We used digitised mammograms for 371 monozygotic twin pairs, aged 40-70 years without a prior diagnosis of breast cancer at the time of mammography, from the Australian Mammographic Density Twins and Sisters Study. We generated normalised, age-adjusted, and standardised risk scores based on textures using the Cirrus algorithm and on three spatially independent dense areas defined by increasing brightness threshold: light areas, bright areas, and brightest areas. Causal inference was made using the Inference about Causation from Examination of FAmilial CONfounding (ICE FALCON) method. Results The mammogram risk scores were correlated within twin pairs and with each other (r = 0.22-0.81; all P < 0.005). We estimated that 28-92% of the associations between the risk scores could be attributed to causal relationships between the scores, with the rest attributed to familial confounders shared by the scores. There was consistent evidence for positive causal effects: of Cirrus, light areas, and bright areas on the brightest areas (accounting for 34%, 55%, and 85% of the associations, respectively); and of light areas and bright areas on Cirrus (accounting for 37% and 28%, respectively). Conclusions In a mammogram, the lighter (less dense) areas have a causal effect on the brightest (highly dense) areas, including through a causal pathway via textural features. These causal relationships help us gain insight into the relative aetiological importance of different mammographic features in breast cancer. For example our findings are consistent with the brightest areas being more aetiologically important than lighter areas for screen-detected breast cancer; conversely, light areas being more aetiologically important for interval breast cancer. Additionally, specific textural features capture aetiologically independent breast cancer risk information from dense areas. These findings highlight the utility of ICE FALCON and family data in decomposing the associations between intercorrelated disease biomarkers into distinct biological pathways. Keywords: Breast cancer, Mammographic density, Textural feature, ICE FALCON, Causal inference |
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AbstractList | Mammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk differently and could reveal distinct information about breast cancer risk. We aimed to investigate causal relationships between these intercorrelated mammogram risk scores to determine their relevance to breast cancer aetiology. We used digitised mammograms for 371 monozygotic twin pairs, aged 40-70 years without a prior diagnosis of breast cancer at the time of mammography, from the Australian Mammographic Density Twins and Sisters Study. We generated normalised, age-adjusted, and standardised risk scores based on textures using the Cirrus algorithm and on three spatially independent dense areas defined by increasing brightness threshold: light areas, bright areas, and brightest areas. Causal inference was made using the Inference about Causation from Examination of FAmilial CONfounding (ICE FALCON) method. The mammogram risk scores were correlated within twin pairs and with each other (r = 0.22-0.81; all P < 0.005). We estimated that 28-92% of the associations between the risk scores could be attributed to causal relationships between the scores, with the rest attributed to familial confounders shared by the scores. There was consistent evidence for positive causal effects: of Cirrus, light areas, and bright areas on the brightest areas (accounting for 34%, 55%, and 85% of the associations, respectively); and of light areas and bright areas on Cirrus (accounting for 37% and 28%, respectively). In a mammogram, the lighter (less dense) areas have a causal effect on the brightest (highly dense) areas, including through a causal pathway via textural features. These causal relationships help us gain insight into the relative aetiological importance of different mammographic features in breast cancer. For example our findings are consistent with the brightest areas being more aetiologically important than lighter areas for screen-detected breast cancer; conversely, light areas being more aetiologically important for interval breast cancer. Additionally, specific textural features capture aetiologically independent breast cancer risk information from dense areas. These findings highlight the utility of ICE FALCON and family data in decomposing the associations between intercorrelated disease biomarkers into distinct biological pathways. BACKGROUNDMammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk differently and could reveal distinct information about breast cancer risk. We aimed to investigate causal relationships between these intercorrelated mammogram risk scores to determine their relevance to breast cancer aetiology.METHODSWe used digitised mammograms for 371 monozygotic twin pairs, aged 40-70 years without a prior diagnosis of breast cancer at the time of mammography, from the Australian Mammographic Density Twins and Sisters Study. We generated normalised, age-adjusted, and standardised risk scores based on textures using the Cirrus algorithm and on three spatially independent dense areas defined by increasing brightness threshold: light areas, bright areas, and brightest areas. Causal inference was made using the Inference about Causation from Examination of FAmilial CONfounding (ICE FALCON) method.RESULTSThe mammogram risk scores were correlated within twin pairs and with each other (r = 0.22-0.81; all P < 0.005). We estimated that 28-92% of the associations between the risk scores could be attributed to causal relationships between the scores, with the rest attributed to familial confounders shared by the scores. There was consistent evidence for positive causal effects: of Cirrus, light areas, and bright areas on the brightest areas (accounting for 34%, 55%, and 85% of the associations, respectively); and of light areas and bright areas on Cirrus (accounting for 37% and 28%, respectively).CONCLUSIONSIn a mammogram, the lighter (less dense) areas have a causal effect on the brightest (highly dense) areas, including through a causal pathway via textural features. These causal relationships help us gain insight into the relative aetiological importance of different mammographic features in breast cancer. For example our findings are consistent with the brightest areas being more aetiologically important than lighter areas for screen-detected breast cancer; conversely, light areas being more aetiologically important for interval breast cancer. Additionally, specific textural features capture aetiologically independent breast cancer risk information from dense areas. These findings highlight the utility of ICE FALCON and family data in decomposing the associations between intercorrelated disease biomarkers into distinct biological pathways. Abstract Background Mammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk differently and could reveal distinct information about breast cancer risk. We aimed to investigate causal relationships between these intercorrelated mammogram risk scores to determine their relevance to breast cancer aetiology. Methods We used digitised mammograms for 371 monozygotic twin pairs, aged 40–70 years without a prior diagnosis of breast cancer at the time of mammography, from the Australian Mammographic Density Twins and Sisters Study. We generated normalised, age-adjusted, and standardised risk scores based on textures using the Cirrus algorithm and on three spatially independent dense areas defined by increasing brightness threshold: light areas, bright areas, and brightest areas. Causal inference was made using the Inference about Causation from Examination of FAmilial CONfounding (ICE FALCON) method. Results The mammogram risk scores were correlated within twin pairs and with each other (r = 0.22–0.81; all P < 0.005). We estimated that 28–92% of the associations between the risk scores could be attributed to causal relationships between the scores, with the rest attributed to familial confounders shared by the scores. There was consistent evidence for positive causal effects: of Cirrus, light areas, and bright areas on the brightest areas (accounting for 34%, 55%, and 85% of the associations, respectively); and of light areas and bright areas on Cirrus (accounting for 37% and 28%, respectively). Conclusions In a mammogram, the lighter (less dense) areas have a causal effect on the brightest (highly dense) areas, including through a causal pathway via textural features. These causal relationships help us gain insight into the relative aetiological importance of different mammographic features in breast cancer. For example our findings are consistent with the brightest areas being more aetiologically important than lighter areas for screen-detected breast cancer; conversely, light areas being more aetiologically important for interval breast cancer. Additionally, specific textural features capture aetiologically independent breast cancer risk information from dense areas. These findings highlight the utility of ICE FALCON and family data in decomposing the associations between intercorrelated disease biomarkers into distinct biological pathways. Background Mammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk differently and could reveal distinct information about breast cancer risk. We aimed to investigate causal relationships between these intercorrelated mammogram risk scores to determine their relevance to breast cancer aetiology. Methods We used digitised mammograms for 371 monozygotic twin pairs, aged 40-70 years without a prior diagnosis of breast cancer at the time of mammography, from the Australian Mammographic Density Twins and Sisters Study. We generated normalised, age-adjusted, and standardised risk scores based on textures using the Cirrus algorithm and on three spatially independent dense areas defined by increasing brightness threshold: light areas, bright areas, and brightest areas. Causal inference was made using the Inference about Causation from Examination of FAmilial CONfounding (ICE FALCON) method. Results The mammogram risk scores were correlated within twin pairs and with each other (r = 0.22-0.81; all P < 0.005). We estimated that 28-92% of the associations between the risk scores could be attributed to causal relationships between the scores, with the rest attributed to familial confounders shared by the scores. There was consistent evidence for positive causal effects: of Cirrus, light areas, and bright areas on the brightest areas (accounting for 34%, 55%, and 85% of the associations, respectively); and of light areas and bright areas on Cirrus (accounting for 37% and 28%, respectively). Conclusions In a mammogram, the lighter (less dense) areas have a causal effect on the brightest (highly dense) areas, including through a causal pathway via textural features. These causal relationships help us gain insight into the relative aetiological importance of different mammographic features in breast cancer. For example our findings are consistent with the brightest areas being more aetiologically important than lighter areas for screen-detected breast cancer; conversely, light areas being more aetiologically important for interval breast cancer. Additionally, specific textural features capture aetiologically independent breast cancer risk information from dense areas. These findings highlight the utility of ICE FALCON and family data in decomposing the associations between intercorrelated disease biomarkers into distinct biological pathways. Keywords: Breast cancer, Mammographic density, Textural feature, ICE FALCON, Causal inference |
ArticleNumber | 127 |
Audience | Academic |
Author | Evans, Christopher F Tan, Maxine Hopper, John L Ye, Zhoufeng Schmidt, Daniel F Sung, Joohon Li, Shuai Giles, Graham G MacInnis, Robert J Esser, Vivienne F. C Dite, Gillian S Al-Qershi, Osamah M Dowty, James G Southey, Melissa C Makalic, Enes Jenkins, Mark A Bui, Minh Nguyen, Tuong L Trinh, Ho N |
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References | TL Nguyen (1733_CR3) 2015; 17 K Krishnan (1733_CR32) 2017; 26 CG Davey (1733_CR25) 2016; 46 A Gastounioti (1733_CR7) 2016; 18 M Bui (1733_CR26) 2013; 55 A Fischmann (1733_CR33) 2005; 78 MM Haby (1733_CR20) 2012; 27 S Li (1733_CR16) 2020; 49 S Li (1733_CR28) 2019; 43 CM Vachon (1733_CR34) 2007; 9 RR Winkel (1733_CR13) 2016; 16 TL Nguyen (1733_CR5) 2018; 20 1733_CR30 JL Hopper (1733_CR36) 1992; 136 S Li (1733_CR27) 2018; 10 TL Nguyen (1733_CR37) 2013; 22 TL Nguyen (1733_CR4) 2017; 46 TL Nguyen (1733_CR11) 2018; 286 A Pettersson (1733_CR35) 2014; 106 ET Warner (1733_CR12) 2021; 7 J Stone (1733_CR23) 2012; 21 GP Watt (1733_CR6) 2022; 151 TL Nguyen (1733_CR10) 2021; 148 S Li (1733_CR19) 2022; 14 JM Robins (1733_CR14) 1999; 121 MJ Yaffe (1733_CR1) 2008; 10 NF Boyd (1733_CR2) 2007; 356 DF Schmidt (1733_CR8) 2018; 2 N Holowko (1733_CR38) 2020; 80 NF Boyd (1733_CR18) 2002; 347 JL Hopper (1733_CR24) 2012; 130 JL Hopper (1733_CR9) 2020; 9 F Odefrey (1733_CR17) 2010; 70 S Wright (1733_CR29) 1934; 5 GEP Box (1733_CR21) 1964; 26 TL Nguyen (1733_CR15) 2022; 14 GS Dite (1733_CR22) 2008; 17 J Stone (1733_CR31) 2010; 12 |
References_xml | – volume: 10 start-page: 209 issue: 3 year: 2008 ident: 1733_CR1 publication-title: Breast Cancer Res doi: 10.1186/bcr2102 contributor: fullname: MJ Yaffe – volume: 12 start-page: 1 issue: 6 year: 2010 ident: 1733_CR31 publication-title: Breast Cancer Res doi: 10.1186/bcr2778 contributor: fullname: J Stone – volume: 2 start-page: pky057 issue: 4 year: 2018 ident: 1733_CR8 publication-title: JNCI Cancer Spectr. doi: 10.1093/jncics/pky057 contributor: fullname: DF Schmidt – volume: 49 start-page: 1259 issue: 4 year: 2020 ident: 1733_CR16 publication-title: Int J Epidemiol doi: 10.1093/ije/dyaa065 contributor: fullname: S Li – volume: 22 start-page: 2395 issue: 12 year: 2013 ident: 1733_CR37 publication-title: Cancer Epidemiol Biomarkers Prev doi: 10.1158/1055-9965.EPI-13-0481 contributor: fullname: TL Nguyen – volume: 78 start-page: 312 issue: 928 year: 2005 ident: 1733_CR33 publication-title: Br J Radiol doi: 10.1259/bjr/33317317 contributor: fullname: A Fischmann – volume: 9 start-page: 217 issue: 6 year: 2007 ident: 1733_CR34 publication-title: Breast Cancer Res doi: 10.1186/bcr1829 contributor: fullname: CM Vachon – volume: 70 start-page: 1449 issue: 4 year: 2010 ident: 1733_CR17 publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-09-3495 contributor: fullname: F Odefrey – volume: 46 start-page: 3213 issue: 15 year: 2016 ident: 1733_CR25 publication-title: Psychol Med doi: 10.1017/S0033291716001884 contributor: fullname: CG Davey – volume: 356 start-page: 227 issue: 3 year: 2007 ident: 1733_CR2 publication-title: N Engl J Med doi: 10.1056/NEJMoa062790 contributor: fullname: NF Boyd – volume: 18 start-page: 91 issue: 1 year: 2016 ident: 1733_CR7 publication-title: Breast Cancer Res doi: 10.1186/s13058-016-0755-8 contributor: fullname: A Gastounioti – volume: 27 start-page: 250 issue: 2 year: 2012 ident: 1733_CR20 publication-title: Health Promot Int doi: 10.1093/heapro/dar036 contributor: fullname: MM Haby – volume: 16 start-page: 1 issue: 1 year: 2016 ident: 1733_CR13 publication-title: BMC Cancer doi: 10.1186/s12885-016-2450-7 contributor: fullname: RR Winkel – volume: 347 start-page: 886 issue: 12 year: 2002 ident: 1733_CR18 publication-title: N Engl J Med doi: 10.1056/NEJMoa013390 contributor: fullname: NF Boyd – volume: 21 start-page: 1149 issue: 7 year: 2012 ident: 1733_CR23 publication-title: Cancer Epidemiol Biomarkers Prev doi: 10.1158/1055-9965.EPI-12-0051 contributor: fullname: J Stone – volume: 26 start-page: 211 issue: 2 year: 1964 ident: 1733_CR21 publication-title: J R Stat Soc Ser B (Methodol) doi: 10.1111/j.2517-6161.1964.tb00553.x contributor: fullname: GEP Box – volume: 151 start-page: 1304 issue: 8 year: 2022 ident: 1733_CR6 publication-title: Int J Cancer doi: 10.1002/ijc.34001 contributor: fullname: GP Watt – volume: 148 start-page: 2193 issue: 9 year: 2021 ident: 1733_CR10 publication-title: Int J Cancer doi: 10.1002/ijc.33396 contributor: fullname: TL Nguyen – volume: 17 start-page: 142 year: 2015 ident: 1733_CR3 publication-title: Breast Cancer Res doi: 10.1186/s13058-015-0654-4 contributor: fullname: TL Nguyen – volume: 46 start-page: 652 issue: 2 year: 2017 ident: 1733_CR4 publication-title: Int J Epidemiol contributor: fullname: TL Nguyen – volume: 10 start-page: 18 year: 2018 ident: 1733_CR27 publication-title: Clin Epigenetics doi: 10.1186/s13148-018-0452-9 contributor: fullname: S Li – volume: 26 start-page: 651 issue: 4 year: 2017 ident: 1733_CR32 publication-title: Cancer Epidemiol Biomarkers Prev doi: 10.1158/1055-9965.EPI-16-0499 contributor: fullname: K Krishnan – volume: 106 start-page: dju078 issue: 5 year: 2014 ident: 1733_CR35 publication-title: J Natl Cancer Inst doi: 10.1093/jnci/dju078 contributor: fullname: A Pettersson – volume: 43 start-page: 243 issue: 2 year: 2019 ident: 1733_CR28 publication-title: Int J Obes doi: 10.1038/s41366-018-0103-4 contributor: fullname: S Li – volume: 55 start-page: 353 issue: 2 year: 2013 ident: 1733_CR26 publication-title: Bone doi: 10.1016/j.bone.2013.04.020 contributor: fullname: M Bui – volume: 121 start-page: 151 issue: 1/2 year: 1999 ident: 1733_CR14 publication-title: Synthese doi: 10.1023/A:1005285815569 contributor: fullname: JM Robins – volume: 286 start-page: 433 issue: 2 year: 2018 ident: 1733_CR11 publication-title: Radiology doi: 10.1148/radiol.2017170306 contributor: fullname: TL Nguyen – volume: 17 start-page: 3474 issue: 12 year: 2008 ident: 1733_CR22 publication-title: Cancer Epidemiol Biomarkers Prev doi: 10.1158/1055-9965.EPI-07-2636 contributor: fullname: GS Dite – volume: 130 start-page: 1117 issue: 5 year: 2012 ident: 1733_CR24 publication-title: J Allergy Clin Immunol doi: 10.1016/j.jaci.2012.08.003 contributor: fullname: JL Hopper – volume: 136 start-page: 1138 issue: 9 year: 1992 ident: 1733_CR36 publication-title: Am J Epidemiol doi: 10.1093/oxfordjournals.aje.a116580 contributor: fullname: JL Hopper – volume: 9 start-page: 627 issue: 3 year: 2020 ident: 1733_CR9 publication-title: J Clin Med doi: 10.3390/jcm9030627 contributor: fullname: JL Hopper – volume: 14 start-page: 1483 issue: 6 year: 2022 ident: 1733_CR15 publication-title: Cancers (Basel). doi: 10.3390/cancers14061483 contributor: fullname: TL Nguyen – volume: 5 start-page: 161 issue: 3 year: 1934 ident: 1733_CR29 publication-title: Ann Math Stat doi: 10.1214/aoms/1177732676 contributor: fullname: S Wright – volume: 80 start-page: 1590 issue: 7 year: 2020 ident: 1733_CR38 publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-19-2455 contributor: fullname: N Holowko – volume: 7 start-page: 68 issue: 1 year: 2021 ident: 1733_CR12 publication-title: NPJ Breast Cancer doi: 10.1038/s41523-021-00272-2 contributor: fullname: ET Warner – volume: 20 start-page: 152 issue: 1 year: 2018 ident: 1733_CR5 publication-title: Breast Cancer Res doi: 10.1186/s13058-018-1081-0 contributor: fullname: TL Nguyen – volume: 14 start-page: 2767 issue: 11 year: 2022 ident: 1733_CR19 publication-title: Cancers (Basel). doi: 10.3390/cancers14112767 contributor: fullname: S Li – ident: 1733_CR30 |
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Snippet | Background Mammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk differently and... Mammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk differently and could... BackgroundMammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk differently and... BACKGROUNDMammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk differently and... Abstract Background Mammogram risk scores based on texture and density defined by different brightness thresholds are associated with breast cancer risk... |
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SubjectTerms | Age Algorithms Automation Body mass index Breast cancer Brightness Cancer Causal inference Epidemiology Family medical history Health aspects ICE FALCON Light Light effects Mammographic density Mammography Oncology, Experimental Questionnaires Risk factors Software Textural feature Twins |
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Title | Causal relationships between breast cancer risk factors based on mammographic features |
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