Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics

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Region Hovedstaden - en del af Københavns Universitetshospital

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Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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Ostrom, QT, Egan, KM, Nabors, LB, Gerke, T, Thompson, RC, Olson, JJ, LaRocca, R, Chowdhary, S, Eckel-Passow, JE, Armstrong, G, Wiencke, JK, Bernstein, JL, Claus, EB, Il'yasova, D, Johansen, C, Lachance, DH, Lai, RK, Merrell, RT, Olson, SH, Sadetzki, S, Schildkraut, JM, Shete, S, Houlston, RS, Jenkins, RB, Wrensch, MR, Melin, B, Amos, CI, Huse, JT, Barnholtz-Sloan, JS & Bondy, ML 2020, 'Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics', International Journal of Cancer, bind 146, nr. 3, s. 739-748. https://doi.org/10.1002/ijc.32318

APA

Ostrom, Q. T., Egan, K. M., Nabors, L. B., Gerke, T., Thompson, R. C., Olson, J. J., LaRocca, R., Chowdhary, S., Eckel-Passow, J. E., Armstrong, G., Wiencke, J. K., Bernstein, J. L., Claus, E. B., Il'yasova, D., Johansen, C., Lachance, D. H., Lai, R. K., Merrell, R. T., Olson, S. H., ... Bondy, M. L. (2020). Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics. International Journal of Cancer, 146(3), 739-748. https://doi.org/10.1002/ijc.32318

CBE

Ostrom QT, Egan KM, Nabors LB, Gerke T, Thompson RC, Olson JJ, LaRocca R, Chowdhary S, Eckel-Passow JE, Armstrong G, Wiencke JK, Bernstein JL, Claus EB, Il'yasova D, Johansen C, Lachance DH, Lai RK, Merrell RT, Olson SH, Sadetzki S, Schildkraut JM, Shete S, Houlston RS, Jenkins RB, Wrensch MR, Melin B, Amos CI, Huse JT, Barnholtz-Sloan JS, Bondy ML. 2020. Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics. International Journal of Cancer. 146(3):739-748. https://doi.org/10.1002/ijc.32318

MLA

Ostrom, Quinn T o.a.. "Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics". International Journal of Cancer. 2020, 146(3). 739-748. https://doi.org/10.1002/ijc.32318

Vancouver

Ostrom QT, Egan KM, Nabors LB, Gerke T, Thompson RC, Olson JJ o.a. Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics. International Journal of Cancer. 2020 feb 1;146(3):739-748. https://doi.org/10.1002/ijc.32318

Author

Ostrom, Quinn T ; Egan, Kathleen M ; Nabors, L Burt ; Gerke, Travis ; Thompson, Reid C ; Olson, Jeffrey J ; LaRocca, Renato ; Chowdhary, Sajeel ; Eckel-Passow, Jeanette E ; Armstrong, Georgina ; Wiencke, John K ; Bernstein, Jonine L ; Claus, Elizabeth B ; Il'yasova, Dora ; Johansen, Christoffer ; Lachance, Daniel H ; Lai, Rose K ; Merrell, Ryan T ; Olson, Sara H ; Sadetzki, Siegal ; Schildkraut, Joellen M ; Shete, Sanjay ; Houlston, Richard S ; Jenkins, Robert B ; Wrensch, Margaret R ; Melin, Beatrice ; Amos, Christopher I ; Huse, Jason T ; Barnholtz-Sloan, Jill S ; Bondy, Melissa L. / Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics. I: International Journal of Cancer. 2020 ; Bind 146, Nr. 3. s. 739-748.

Bibtex

@article{62e547a8ac3c473f99dbffff28918209,

title = "Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics",

abstract = "Glioma incidence is highest in non-Hispanic Whites, and to date, glioma genome-wide association studies (GWAS) to date have only included European ancestry (EA) populations. African Americans and Hispanics in the US have varying proportions of EA, African (AA) and Native American ancestries (NAA). It is unknown if identified GWAS loci or increased EA is associated with increased glioma risk. We assessed whether EA was associated with glioma in African Americans and Hispanics. Data were obtained for 832 cases and 675 controls from the Glioma International Case-Control Study and GliomaSE Case-Control Study previously estimated to have <80% EA, or self-identify as non-White. We estimated global and local ancestry using fastStructure and RFMix, respectively, using 1,000 genomes project reference populations. Within groups with ≥40% AA (AFR≥0.4 ), and ≥15% NAA (AMR≥0.15 ), genome-wide association between local EA and glioma was evaluated using logistic regression conditioned on global EA for all gliomas. We identified two regions (7q21.11, p = 6.36 × 10-4 ; 11p11.12, p = 7.0 × 10-4 ) associated with increased EA, and one associated with decreased EA (20p12.13, p = 0.0026) in AFR≥0.4 . In addition, we identified a peak at rs1620291 (p = 4.36 × 10-6 ) in 7q21.3. Among AMR≥0.15 , we found an association between increased EA in one region (12q24.21, p = 8.38 × 10-4 ), and decreased EA in two regions (8q24.21, p = 0. 0010; 20q13.33, p = 6.36 × 10-4 ). No other significant associations were identified. This analysis identified an association between glioma and two regions previously identified in EA populations (8q24.21, 20q13.33) and four novel regions (7q21.11, 11p11.12, 12q24.21 and 20p12.13). The identifications of novel association with EA suggest regions to target for future genetic association studies.",

keywords = "genetic ancestry, genetic epidemiology, genome-wide association study, glioma",

author = "Ostrom, {Quinn T} and Egan, {Kathleen M} and Nabors, {L Burt} and Travis Gerke and Thompson, {Reid C} and Olson, {Jeffrey J} and Renato LaRocca and Sajeel Chowdhary and Eckel-Passow, {Jeanette E} and Georgina Armstrong and Wiencke, {John K} and Bernstein, {Jonine L} and Claus, {Elizabeth B} and Dora Il'yasova and Christoffer Johansen and Lachance, {Daniel H} and Lai, {Rose K} and Merrell, {Ryan T} and Olson, {Sara H} and Siegal Sadetzki and Schildkraut, {Joellen M} and Sanjay Shete and Houlston, {Richard S} and Jenkins, {Robert B} and Wrensch, {Margaret R} and Beatrice Melin and Amos, {Christopher I} and Huse, {Jason T} and Barnholtz-Sloan, {Jill S} and Bondy, {Melissa L}",

note = "{\textcopyright} 2019 UICC.",

year = "2020",

month = feb,

day = "1",

doi = "10.1002/ijc.32318",

language = "English",

volume = "146",

pages = "739--748",

journal = "International Journal of Cancer",

issn = "0020-7136",

publisher = "JohnWiley & Sons, Inc",

number = "3",

}

RIS

TY - JOUR

T1 - Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics

AU - Ostrom, Quinn T

AU - Egan, Kathleen M

AU - Nabors, L Burt

AU - Gerke, Travis

AU - Thompson, Reid C

AU - Olson, Jeffrey J

AU - LaRocca, Renato

AU - Chowdhary, Sajeel

AU - Eckel-Passow, Jeanette E

AU - Armstrong, Georgina

AU - Wiencke, John K

AU - Bernstein, Jonine L

AU - Claus, Elizabeth B

AU - Il'yasova, Dora

AU - Johansen, Christoffer

AU - Lachance, Daniel H

AU - Lai, Rose K

AU - Merrell, Ryan T

AU - Olson, Sara H

AU - Sadetzki, Siegal

AU - Schildkraut, Joellen M

AU - Shete, Sanjay

AU - Houlston, Richard S

AU - Jenkins, Robert B

AU - Wrensch, Margaret R

AU - Melin, Beatrice

AU - Amos, Christopher I

AU - Huse, Jason T

AU - Barnholtz-Sloan, Jill S

AU - Bondy, Melissa L

PY - 2020/2/1

Y1 - 2020/2/1

N2 - Glioma incidence is highest in non-Hispanic Whites, and to date, glioma genome-wide association studies (GWAS) to date have only included European ancestry (EA) populations. African Americans and Hispanics in the US have varying proportions of EA, African (AA) and Native American ancestries (NAA). It is unknown if identified GWAS loci or increased EA is associated with increased glioma risk. We assessed whether EA was associated with glioma in African Americans and Hispanics. Data were obtained for 832 cases and 675 controls from the Glioma International Case-Control Study and GliomaSE Case-Control Study previously estimated to have <80% EA, or self-identify as non-White. We estimated global and local ancestry using fastStructure and RFMix, respectively, using 1,000 genomes project reference populations. Within groups with ≥40% AA (AFR≥0.4 ), and ≥15% NAA (AMR≥0.15 ), genome-wide association between local EA and glioma was evaluated using logistic regression conditioned on global EA for all gliomas. We identified two regions (7q21.11, p = 6.36 × 10-4 ; 11p11.12, p = 7.0 × 10-4 ) associated with increased EA, and one associated with decreased EA (20p12.13, p = 0.0026) in AFR≥0.4 . In addition, we identified a peak at rs1620291 (p = 4.36 × 10-6 ) in 7q21.3. Among AMR≥0.15 , we found an association between increased EA in one region (12q24.21, p = 8.38 × 10-4 ), and decreased EA in two regions (8q24.21, p = 0. 0010; 20q13.33, p = 6.36 × 10-4 ). No other significant associations were identified. This analysis identified an association between glioma and two regions previously identified in EA populations (8q24.21, 20q13.33) and four novel regions (7q21.11, 11p11.12, 12q24.21 and 20p12.13). The identifications of novel association with EA suggest regions to target for future genetic association studies.

AB - Glioma incidence is highest in non-Hispanic Whites, and to date, glioma genome-wide association studies (GWAS) to date have only included European ancestry (EA) populations. African Americans and Hispanics in the US have varying proportions of EA, African (AA) and Native American ancestries (NAA). It is unknown if identified GWAS loci or increased EA is associated with increased glioma risk. We assessed whether EA was associated with glioma in African Americans and Hispanics. Data were obtained for 832 cases and 675 controls from the Glioma International Case-Control Study and GliomaSE Case-Control Study previously estimated to have <80% EA, or self-identify as non-White. We estimated global and local ancestry using fastStructure and RFMix, respectively, using 1,000 genomes project reference populations. Within groups with ≥40% AA (AFR≥0.4 ), and ≥15% NAA (AMR≥0.15 ), genome-wide association between local EA and glioma was evaluated using logistic regression conditioned on global EA for all gliomas. We identified two regions (7q21.11, p = 6.36 × 10-4 ; 11p11.12, p = 7.0 × 10-4 ) associated with increased EA, and one associated with decreased EA (20p12.13, p = 0.0026) in AFR≥0.4 . In addition, we identified a peak at rs1620291 (p = 4.36 × 10-6 ) in 7q21.3. Among AMR≥0.15 , we found an association between increased EA in one region (12q24.21, p = 8.38 × 10-4 ), and decreased EA in two regions (8q24.21, p = 0. 0010; 20q13.33, p = 6.36 × 10-4 ). No other significant associations were identified. This analysis identified an association between glioma and two regions previously identified in EA populations (8q24.21, 20q13.33) and four novel regions (7q21.11, 11p11.12, 12q24.21 and 20p12.13). The identifications of novel association with EA suggest regions to target for future genetic association studies.

KW - genetic ancestry

KW - genetic epidemiology

KW - genome-wide association study

KW - glioma

UR - http://www.scopus.com/inward/record.url?scp=85064651435&partnerID=8YFLogxK

U2 - 10.1002/ijc.32318

DO - 10.1002/ijc.32318

M3 - Journal article

C2 - 30963577

VL - 146

SP - 739

EP - 748

JO - International Journal of Cancer

JF - International Journal of Cancer

SN - 0020-7136

IS - 3

ER -

ID: 57382655