Blood-based omic profiling supports female susceptibility to tobacco smoke-induced cardiovascular diseases

Aristotelis Chatziioannou; Panagiotis Georgiadis; Dennie G. Hebels; Irene Liampa; Ioannis Valavanis; Ingvar A. Bergdahl; Anders Johansson; Domenico Palli; Marc Chadeau-Hyam; Alexandros P. Siskos; Hector Keun; Maria Botsivali; Theo M.C.M. De Kok; Almudena Espín Pérez; Jos C.S. Kleinjans; Paolo Vineis; Soterios A. Kyrtopoulos; Ralph Gottschalk; Danitsja Van Leeuwen; Leen Timmermans; Benedetta Bendinelli; Rachel Kelly; Roel Vermeulen; Lutzen Portengen; Fatemeh Saberi-Hosnijeh; Beatrice Melin; Goran Hallmans; Per Lenner; Toby J. Athersuch; Manolis Kogevinas; Euripides G. Stephanou; Antonis Myridakis; Lucia Fazzo; Marco De Santis; Pietro Comba; Hannu Kiviranta; Panu Rantakokko; Riikka Airaksinen; Paivi Ruokojarvi; Mark Gilthorpe; Sarah Fleming; Thomas Fleming; Yu Kang Tu; Bo Jonsson; Thomas Lundh; Wei J. Chen; Wen Chung Lee; Chuhsing Kate Hsiao; Kuo Liong Chien; Po Hsiu Kuo; Hung Hung; Shu Fen Liao

doi:10.1038/srep42870

Blood-based omic profiling supports female susceptibility to tobacco smoke-induced cardiovascular diseases

Aristotelis Chatziioannou, Panagiotis Georgiadis, Dennie G. Hebels, Irene Liampa, Ioannis Valavanis, Ingvar A. Bergdahl, Anders Johansson, Domenico Palli, Marc Chadeau-Hyam, Alexandros P. Siskos, Hector Keun, Maria Botsivali, Theo M.C.M. De Kok, Almudena Espín Pérez, Jos C.S. Kleinjans, Paolo Vineis, Soterios A. Kyrtopoulos, Ralph Gottschalk, Danitsja Van Leeuwen, Leen TimmermansBenedetta Bendinelli, Rachel Kelly, Roel Vermeulen, Lutzen Portengen, Fatemeh Saberi-Hosnijeh, Beatrice Melin, Goran Hallmans, Per Lenner, Toby J. Athersuch, Manolis Kogevinas, Euripides G. Stephanou, Antonis Myridakis, Lucia Fazzo, Marco De Santis, Pietro Comba, Hannu Kiviranta, Panu Rantakokko, Riikka Airaksinen, Paivi Ruokojarvi, Mark Gilthorpe, Sarah Fleming, Thomas Fleming, Yu Kang Tu, Bo Jonsson, Thomas Lundh, Wei J. Chen, Wen Chung Lee, Chuhsing Kate Hsiao, Kuo Liong Chien, Po Hsiu Kuo, Hung Hung, Shu Fen Liao

Research output: Contribution to journal › Article › peer-review

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Abstract

We recently reported that differential gene expression and DNA methylation profiles in blood leukocytes of apparently healthy smokers predicts with remarkable efficiency diseases and conditions known to be causally associated with smoking, suggesting that blood-based omic profiling of human populations may be useful for linking environmental exposures to potential health effects. Here we report on the sex-specific effects of tobacco smoking on transcriptomic and epigenetic features derived from genome-wide profiling in white blood cells, identifying 26 expression probes and 92 CpG sites, almost all of which are affected only in female smokers. Strikingly, these features relate to numerous genes with a key role in the pathogenesis of cardiovascular disease, especially thrombin signaling, including the thrombin receptors on platelets F2R (coagulation factor II (thrombin) receptor; PAR1) and GP5 (glycoprotein 5), as well as HMOX1 (haem oxygenase 1) and BCL2L1 (BCL2-like 1) which are involved in protection against oxidative stress and apoptosis, respectively. These results are in concordance with epidemiological evidence of higher female susceptibility to tobacco-induced cardiovascular disease and underline the potential of blood-based omic profiling in hazard and risk assessment.

Original language	English
Article number	42870
Journal	Scientific Reports
Volume	7
DOIs	https://doi.org/10.1038/srep42870
Publication status	Published - Feb 2017
Externally published	Yes

ASJC Scopus subject areas

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This output contributes to the following UN Sustainable Development Goals (SDGs)

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Chatziioannou, A., Georgiadis, P., Hebels, D. G., Liampa, I., Valavanis, I., Bergdahl, I. A., Johansson, A., Palli, D., Chadeau-Hyam, M., Siskos, A. P., Keun, H., Botsivali, M., De Kok, T. M. C. M., Pérez, A. E., Kleinjans, J. C. S., Vineis, P., Kyrtopoulos, S. A., Gottschalk, R., Van Leeuwen, D., ... Liao, S. F. (2017). Blood-based omic profiling supports female susceptibility to tobacco smoke-induced cardiovascular diseases. Scientific Reports, 7, Article 42870. https://doi.org/10.1038/srep42870

Chatziioannou, A, Georgiadis, P, Hebels, DG, Liampa, I, Valavanis, I, Bergdahl, IA, Johansson, A, Palli, D, Chadeau-Hyam, M, Siskos, AP, Keun, H, Botsivali, M, De Kok, TMCM, Pérez, AE, Kleinjans, JCS, Vineis, P, Kyrtopoulos, SA, Gottschalk, R, Van Leeuwen, D, Timmermans, L, Bendinelli, B, Kelly, R, Vermeulen, R, Portengen, L, Saberi-Hosnijeh, F, Melin, B, Hallmans, G, Lenner, P, Athersuch, TJ, Kogevinas, M, Stephanou, EG, Myridakis, A, Fazzo, L, De Santis, M, Comba, P, Kiviranta, H, Rantakokko, P, Airaksinen, R, Ruokojarvi, P, Gilthorpe, M, Fleming, S, Fleming, T, Tu, YK, Jonsson, B, Lundh, T, Chen, WJ, Lee, WC, Hsiao, CK, Chien, KL, Kuo, PH, Hung, H & Liao, SF 2017, 'Blood-based omic profiling supports female susceptibility to tobacco smoke-induced cardiovascular diseases', Scientific Reports, vol. 7, 42870. https://doi.org/10.1038/srep42870

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title = "Blood-based omic profiling supports female susceptibility to tobacco smoke-induced cardiovascular diseases",

abstract = "We recently reported that differential gene expression and DNA methylation profiles in blood leukocytes of apparently healthy smokers predicts with remarkable efficiency diseases and conditions known to be causally associated with smoking, suggesting that blood-based omic profiling of human populations may be useful for linking environmental exposures to potential health effects. Here we report on the sex-specific effects of tobacco smoking on transcriptomic and epigenetic features derived from genome-wide profiling in white blood cells, identifying 26 expression probes and 92 CpG sites, almost all of which are affected only in female smokers. Strikingly, these features relate to numerous genes with a key role in the pathogenesis of cardiovascular disease, especially thrombin signaling, including the thrombin receptors on platelets F2R (coagulation factor II (thrombin) receptor; PAR1) and GP5 (glycoprotein 5), as well as HMOX1 (haem oxygenase 1) and BCL2L1 (BCL2-like 1) which are involved in protection against oxidative stress and apoptosis, respectively. These results are in concordance with epidemiological evidence of higher female susceptibility to tobacco-induced cardiovascular disease and underline the potential of blood-based omic profiling in hazard and risk assessment.",

author = "Aristotelis Chatziioannou and Panagiotis Georgiadis and Hebels, {Dennie G.} and Irene Liampa and Ioannis Valavanis and Bergdahl, {Ingvar A.} and Anders Johansson and Domenico Palli and Marc Chadeau-Hyam and Siskos, {Alexandros P.} and Hector Keun and Maria Botsivali and {De Kok}, {Theo M.C.M.} and P{\'e}rez, {Almudena Esp{\'i}n} and Kleinjans, {Jos C.S.} and Paolo Vineis and Kyrtopoulos, {Soterios A.} and Ralph Gottschalk and {Van Leeuwen}, Danitsja and Leen Timmermans and Benedetta Bendinelli and Rachel Kelly and Roel Vermeulen and Lutzen Portengen and Fatemeh Saberi-Hosnijeh and Beatrice Melin and Goran Hallmans and Per Lenner and Athersuch, {Toby J.} and Manolis Kogevinas and Stephanou, {Euripides G.} and Antonis Myridakis and Lucia Fazzo and {De Santis}, Marco and Pietro Comba and Hannu Kiviranta and Panu Rantakokko and Riikka Airaksinen and Paivi Ruokojarvi and Mark Gilthorpe and Sarah Fleming and Thomas Fleming and Tu, {Yu Kang} and Bo Jonsson and Thomas Lundh and Chen, {Wei J.} and Lee, {Wen Chung} and Hsiao, {Chuhsing Kate} and Chien, {Kuo Liong} and Kuo, {Po Hsiu} and Hung Hung and Liao, {Shu Fen}",

note = "Publisher Copyright: {\textcopyright} The Author(s) 2017.",

year = "2017",

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doi = "10.1038/srep42870",

language = "English",

volume = "7",

journal = "Scientific Reports",

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AU - Chatziioannou, Aristotelis

AU - Georgiadis, Panagiotis

AU - Hebels, Dennie G.

AU - Liampa, Irene

AU - Valavanis, Ioannis

AU - Bergdahl, Ingvar A.

AU - Johansson, Anders

AU - Palli, Domenico

AU - Chadeau-Hyam, Marc

AU - Siskos, Alexandros P.

AU - Keun, Hector

AU - Botsivali, Maria

AU - De Kok, Theo M.C.M.

AU - Pérez, Almudena Espín

AU - Kleinjans, Jos C.S.

AU - Vineis, Paolo

AU - Kyrtopoulos, Soterios A.

AU - Gottschalk, Ralph

AU - Van Leeuwen, Danitsja

AU - Timmermans, Leen

AU - Bendinelli, Benedetta

AU - Kelly, Rachel

AU - Vermeulen, Roel

AU - Portengen, Lutzen

AU - Saberi-Hosnijeh, Fatemeh

AU - Melin, Beatrice

AU - Hallmans, Goran

AU - Lenner, Per

AU - Athersuch, Toby J.

AU - Kogevinas, Manolis

AU - Stephanou, Euripides G.

AU - Myridakis, Antonis

AU - Fazzo, Lucia

AU - De Santis, Marco

AU - Comba, Pietro

AU - Kiviranta, Hannu

AU - Rantakokko, Panu

AU - Airaksinen, Riikka

AU - Ruokojarvi, Paivi

AU - Gilthorpe, Mark

AU - Fleming, Sarah

AU - Fleming, Thomas

AU - Tu, Yu Kang

AU - Jonsson, Bo

AU - Lundh, Thomas

AU - Chen, Wei J.

AU - Lee, Wen Chung

AU - Hsiao, Chuhsing Kate

AU - Chien, Kuo Liong

AU - Kuo, Po Hsiu

AU - Hung, Hung

AU - Liao, Shu Fen

PY - 2017/2

Y1 - 2017/2

N2 - We recently reported that differential gene expression and DNA methylation profiles in blood leukocytes of apparently healthy smokers predicts with remarkable efficiency diseases and conditions known to be causally associated with smoking, suggesting that blood-based omic profiling of human populations may be useful for linking environmental exposures to potential health effects. Here we report on the sex-specific effects of tobacco smoking on transcriptomic and epigenetic features derived from genome-wide profiling in white blood cells, identifying 26 expression probes and 92 CpG sites, almost all of which are affected only in female smokers. Strikingly, these features relate to numerous genes with a key role in the pathogenesis of cardiovascular disease, especially thrombin signaling, including the thrombin receptors on platelets F2R (coagulation factor II (thrombin) receptor; PAR1) and GP5 (glycoprotein 5), as well as HMOX1 (haem oxygenase 1) and BCL2L1 (BCL2-like 1) which are involved in protection against oxidative stress and apoptosis, respectively. These results are in concordance with epidemiological evidence of higher female susceptibility to tobacco-induced cardiovascular disease and underline the potential of blood-based omic profiling in hazard and risk assessment.

AB - We recently reported that differential gene expression and DNA methylation profiles in blood leukocytes of apparently healthy smokers predicts with remarkable efficiency diseases and conditions known to be causally associated with smoking, suggesting that blood-based omic profiling of human populations may be useful for linking environmental exposures to potential health effects. Here we report on the sex-specific effects of tobacco smoking on transcriptomic and epigenetic features derived from genome-wide profiling in white blood cells, identifying 26 expression probes and 92 CpG sites, almost all of which are affected only in female smokers. Strikingly, these features relate to numerous genes with a key role in the pathogenesis of cardiovascular disease, especially thrombin signaling, including the thrombin receptors on platelets F2R (coagulation factor II (thrombin) receptor; PAR1) and GP5 (glycoprotein 5), as well as HMOX1 (haem oxygenase 1) and BCL2L1 (BCL2-like 1) which are involved in protection against oxidative stress and apoptosis, respectively. These results are in concordance with epidemiological evidence of higher female susceptibility to tobacco-induced cardiovascular disease and underline the potential of blood-based omic profiling in hazard and risk assessment.

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Blood-based omic profiling supports female susceptibility to tobacco smoke-induced cardiovascular diseases

Abstract

ASJC Scopus subject areas

UN SDGs

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