Skip to main content
Top
Gepubliceerd in: Quality of Life Research 7/2014

01-09-2014 | Review

Biological pathways, candidate genes, and molecular markers associated with quality-of-life domains: an update

Auteurs: Mirjam A. G. Sprangers, Melissa S. Y. Thong, Meike Bartels, Andrea Barsevick, Juan Ordoñana, Qiuling Shi, Xin Shelley Wang, Pål Klepstad, Eddy A. Wierenga, Jasvinder A. Singh, Jeff A. Sloan

Gepubliceerd in: Quality of Life Research | Uitgave 7/2014

Log in om toegang te krijgen
share
DELEN

Deel dit onderdeel of sectie (kopieer de link)

  • Optie A:
    Klik op de rechtermuisknop op de link en selecteer de optie “linkadres kopiëren”
  • Optie B:
    Deel de link per e-mail

Abstract

Background

There is compelling evidence of a genetic foundation of patient-reported quality of life (QOL). Given the rapid development of substantial scientific advances in this area of research, the current paper updates and extends reviews published in 2010.

Objectives

The objective was to provide an updated overview of the biological pathways, candidate genes, and molecular markers involved in fatigue, pain, negative (depressed mood) and positive (well-being/happiness) emotional functioning, social functioning, and overall QOL.

Methods

We followed a purposeful search algorithm of existing literature to capture empirical papers investigating the relationship between biological pathways and molecular markers and the identified QOL domains.

Results

Multiple major pathways are involved in each QOL domain. The inflammatory pathway has the strongest evidence as a controlling mechanism underlying fatigue. Inflammation and neurotransmission are key processes involved in pain perception, and the catechol-O-methyltransferase (COMT) gene is associated with multiple sorts of pain. The neurotransmitter and neuroplasticity theories have the strongest evidence for their relationship with depression. Oxytocin-related genes and genes involved in the serotonergic and dopaminergic pathways play a role in social functioning. Inflammatory pathways, via cytokines, also play an important role in overall QOL.

Conclusions

Whereas the current findings need future experiments and replication efforts, they will provide researchers supportive background information when embarking on studies relating candidate genes and/or molecular markers to QOL domains. The ultimate goal of this area of research is to enhance patients’ QOL.
Bijlagen
Alleen toegankelijk voor geautoriseerde gebruikers
Literatuur
1.
go back to reference Hampton, T. (2004). Patients’ genes may influence quality of life after cancer chemotherapy. JAMA, 292(6), 673–674.PubMed Hampton, T. (2004). Patients’ genes may influence quality of life after cancer chemotherapy. JAMA, 292(6), 673–674.PubMed
2.
go back to reference Sloan, J., & Zhao, X. (2006). Genetics and quality of life. Current Problems in Cancer, 30, 255–260.PubMed Sloan, J., & Zhao, X. (2006). Genetics and quality of life. Current Problems in Cancer, 30, 255–260.PubMed
3.
go back to reference Sprangers, M. A. G., Sloan, J. A., Veenhoven, R., Cleeland, C. S., Halyard, M. Y., Abertnethy, A. M., et al. (2009). The establishment of the GENEQOL Consortium to investigate the genetic disposition of patient-reported quality-of-life outcomes. Twin Research and Human Genetics, 12(3), 301–311.PubMedCentralPubMed Sprangers, M. A. G., Sloan, J. A., Veenhoven, R., Cleeland, C. S., Halyard, M. Y., Abertnethy, A. M., et al. (2009). The establishment of the GENEQOL Consortium to investigate the genetic disposition of patient-reported quality-of-life outcomes. Twin Research and Human Genetics, 12(3), 301–311.PubMedCentralPubMed
4.
go back to reference Sprangers, M. A. G., Sloan, J. A., Barsevick, A., Chauhan, C., Dueck, A. C., Raat, H., et al. (2010). Scientific imperatives, clinical implications, and theoretical underpinnings for the investigation of the relationship between genetic variables and patient-reported quality-of-life outcomes. Quality of Life Research, 19, 1395–1403.PubMedCentralPubMed Sprangers, M. A. G., Sloan, J. A., Barsevick, A., Chauhan, C., Dueck, A. C., Raat, H., et al. (2010). Scientific imperatives, clinical implications, and theoretical underpinnings for the investigation of the relationship between genetic variables and patient-reported quality-of-life outcomes. Quality of Life Research, 19, 1395–1403.PubMedCentralPubMed
5.
go back to reference Bartels, M., Saviouk, V., de Moor, M. H. M., Willemsen, A. H. M., van Beijsterveldt, C. E. M., Hottenga, J. J., et al. (2010). Heritability and genome-wide linkage scan for subjective happiness. Twin Research and Human Genetics, 13(2), 135–142.PubMed Bartels, M., Saviouk, V., de Moor, M. H. M., Willemsen, A. H. M., van Beijsterveldt, C. E. M., Hottenga, J. J., et al. (2010). Heritability and genome-wide linkage scan for subjective happiness. Twin Research and Human Genetics, 13(2), 135–142.PubMed
6.
go back to reference Rausch, S. M., Clark, M. M., Patten, C., Liu, H., Felten, S., Li, Y., et al. (2010). Relationship between cytokine gene single nucleotide polymorphisms and symptom burden and quality of life in lung cancer survivors. Cancer, 116, 4103–4113.PubMedCentralPubMed Rausch, S. M., Clark, M. M., Patten, C., Liu, H., Felten, S., Li, Y., et al. (2010). Relationship between cytokine gene single nucleotide polymorphisms and symptom burden and quality of life in lung cancer survivors. Cancer, 116, 4103–4113.PubMedCentralPubMed
7.
go back to reference Schoormans, D., Radonic, T., de Witte, P., Groenink, M., Azim, D., Lutter, R., et al. (2012). Mental quality of life is related to a cytokine genetic pathway. PLoS ONE, 7(9), e45126.PubMedCentralPubMed Schoormans, D., Radonic, T., de Witte, P., Groenink, M., Azim, D., Lutter, R., et al. (2012). Mental quality of life is related to a cytokine genetic pathway. PLoS ONE, 7(9), e45126.PubMedCentralPubMed
8.
go back to reference Zwinderman, A.H., Sprangers, M.A.G., Baas, F., Van Noorden, C.J., Radbruch, L., Davies, A., Swaab, D.F., et al. (2010). Genes selected for their relevance to pain are also associated with fatigue and dyspnea: Evidence of the European Pharmacogenetic Opioid Study. Annual Conference of the International Society for Quality of Life Research, London. Abstract: NO147. Zwinderman, A.H., Sprangers, M.A.G., Baas, F., Van Noorden, C.J., Radbruch, L., Davies, A., Swaab, D.F., et al. (2010). Genes selected for their relevance to pain are also associated with fatigue and dyspnea: Evidence of the European Pharmacogenetic Opioid Study. Annual Conference of the International Society for Quality of Life Research, London. Abstract: NO147.
9.
go back to reference Shi, Q., Cleeland, C. S., Klepstad, P., Miaskowski, C., & Pedersen, N. L. (2010). Biological pathways and genetic variables involved in pain. Quality of Life Research, 17, 1407–1417. Shi, Q., Cleeland, C. S., Klepstad, P., Miaskowski, C., & Pedersen, N. L. (2010). Biological pathways and genetic variables involved in pain. Quality of Life Research, 17, 1407–1417.
10.
go back to reference Barsevick, A., Frost, M., Zwinderman, A. H., Hall, P., & Halysard, M. (2010). I’m so tired: biological and genetic mechanisms of cancer-related fatigue. Quality of Life Research, 19(10), 1419–1427.PubMedCentralPubMed Barsevick, A., Frost, M., Zwinderman, A. H., Hall, P., & Halysard, M. (2010). I’m so tired: biological and genetic mechanisms of cancer-related fatigue. Quality of Life Research, 19(10), 1419–1427.PubMedCentralPubMed
11.
go back to reference Sprangers, M. A. G., Bartels, M., Veenhoven, R., Baas, F., Martin, N. G., Mosing, M., et al. (2010). Which patient will feel down, which will be happy? The need to study genetic disposition of emotional states. Quality of Life Research, 19, 1429–1437.PubMedCentralPubMed Sprangers, M. A. G., Bartels, M., Veenhoven, R., Baas, F., Martin, N. G., Mosing, M., et al. (2010). Which patient will feel down, which will be happy? The need to study genetic disposition of emotional states. Quality of Life Research, 19, 1429–1437.PubMedCentralPubMed
12.
go back to reference Ordoñana, J. R., Bartels, M., Boomsma, D. I., Cella, D., Mosing, M., Oliveira, J. R., et al. (2013). Biological pathways and genetic mechanisms involved in social functioning. Quality of Life Research, 22(6), 1189–1200.PubMed Ordoñana, J. R., Bartels, M., Boomsma, D. I., Cella, D., Mosing, M., Oliveira, J. R., et al. (2013). Biological pathways and genetic mechanisms involved in social functioning. Quality of Life Research, 22(6), 1189–1200.PubMed
13.
go back to reference Thornton, L. M., Andersen, B. L., & Blakely, W. P. (2010). The pain, depression, and fatigue symptom cluster in advanced breast cancer: Covariation with the hypothalamic-pituitary-adrenal axis and the sympathetic nervous system. Health Psychology, 29(3), 333–337.PubMedCentralPubMed Thornton, L. M., Andersen, B. L., & Blakely, W. P. (2010). The pain, depression, and fatigue symptom cluster in advanced breast cancer: Covariation with the hypothalamic-pituitary-adrenal axis and the sympathetic nervous system. Health Psychology, 29(3), 333–337.PubMedCentralPubMed
14.
go back to reference Saligan, L. N., & Kim, H. S. (2012). A systematic review of the association between immunogenomic markers and cancer-related fatigue. Brain, Behavior, and Immunity, 26(6), 830–848.PubMedCentralPubMed Saligan, L. N., & Kim, H. S. (2012). A systematic review of the association between immunogenomic markers and cancer-related fatigue. Brain, Behavior, and Immunity, 26(6), 830–848.PubMedCentralPubMed
15.
go back to reference Aouizerat, B. E., Dodd, M., Lee, K., West, C., Paul, S. M., Cooper, B. A., et al. (2009). Preliminary evidence of a genetic association between tumor necrosis factor alpha and the severity of sleep disturbance and morning fatigue. Biological Research for Nursing, 11(1), 27–41.PubMed Aouizerat, B. E., Dodd, M., Lee, K., West, C., Paul, S. M., Cooper, B. A., et al. (2009). Preliminary evidence of a genetic association between tumor necrosis factor alpha and the severity of sleep disturbance and morning fatigue. Biological Research for Nursing, 11(1), 27–41.PubMed
16.
go back to reference Collado-Hidalgo, A., Bower, J. E., Ganz, P. A., Irwin, M. R., & Cole, S. W. (2008). Cytokine gene polymorphisms and fatigue in breast cancer survivors: Early findings. Brain, Behavior, and Immunity, 22(8), 1197–1200.PubMedCentralPubMed Collado-Hidalgo, A., Bower, J. E., Ganz, P. A., Irwin, M. R., & Cole, S. W. (2008). Cytokine gene polymorphisms and fatigue in breast cancer survivors: Early findings. Brain, Behavior, and Immunity, 22(8), 1197–1200.PubMedCentralPubMed
17.
go back to reference Platten, M., Wick, W., & Van den Eynde, B. J. (2012). Tryptophan catabolism in cancer: beyond IDO and tryptophan depletion. Cancer Research, 72(21), 5435–5440.PubMed Platten, M., Wick, W., & Van den Eynde, B. J. (2012). Tryptophan catabolism in cancer: beyond IDO and tryptophan depletion. Cancer Research, 72(21), 5435–5440.PubMed
18.
go back to reference Schroecksnadel, K., Fiegl, M., Prassl, K., Winkler, C., Denz, H. A., & Fuchs, D. (2007). Diminished quality of life in patients with cancer correlates with tryptophan degradation. Journal of Cancer Research and Clinical Oncology, 133(7), 477–485.PubMed Schroecksnadel, K., Fiegl, M., Prassl, K., Winkler, C., Denz, H. A., & Fuchs, D. (2007). Diminished quality of life in patients with cancer correlates with tryptophan degradation. Journal of Cancer Research and Clinical Oncology, 133(7), 477–485.PubMed
19.
go back to reference Jun, S. E., Kohen, R., Cain, K. C., Jarrett, M. E., & Heitkemper, M. M. (2014). TPH Gene polymorphisms are associated with disease perception and quality of life in women with irritable bowel syndrome. Biological Research for Nursing, 16(1), 95–104.PubMed Jun, S. E., Kohen, R., Cain, K. C., Jarrett, M. E., & Heitkemper, M. M. (2014). TPH Gene polymorphisms are associated with disease perception and quality of life in women with irritable bowel syndrome. Biological Research for Nursing, 16(1), 95–104.PubMed
20.
go back to reference Fernandez-de-Las-Penas, C., Cantarero-Villanueva, I., Fernandez-Lao, C., Ambite-Quesada, S., Diaz-Rodriquez, L., Rivas-Martinez, I., et al. (2012). Influence of catechol-o-methyltransferase genotype (Val158Met) on endocrine, sympathetic nervous and mucosal immune systems in breast cancer survivors. Breast, 21(2), 199–203.PubMed Fernandez-de-Las-Penas, C., Cantarero-Villanueva, I., Fernandez-Lao, C., Ambite-Quesada, S., Diaz-Rodriquez, L., Rivas-Martinez, I., et al. (2012). Influence of catechol-o-methyltransferase genotype (Val158Met) on endocrine, sympathetic nervous and mucosal immune systems in breast cancer survivors. Breast, 21(2), 199–203.PubMed
21.
go back to reference Lim, J., Ebstein, R., Tse, C. Y., Monakhov, M., Lai, P. S., Dinges, D. F., et al. (2012). Dopaminergic polymorphisms associated with time-on-task declines and fatigue in the Psychomotor Vigilance Test. PLoS ONE, 7(3), e33767.PubMedCentralPubMed Lim, J., Ebstein, R., Tse, C. Y., Monakhov, M., Lai, P. S., Dinges, D. F., et al. (2012). Dopaminergic polymorphisms associated with time-on-task declines and fatigue in the Psychomotor Vigilance Test. PLoS ONE, 7(3), e33767.PubMedCentralPubMed
22.
go back to reference Sloan, J. A., de Andrade, M., Decker, P., Wampfler, J., Oswold, C., Clark, M., et al. (2012). Genetic variations and patient-reported quality of life among patients with lung cancer. Journal of Clinical Oncology, 30, 1–9. Sloan, J. A., de Andrade, M., Decker, P., Wampfler, J., Oswold, C., Clark, M., et al. (2012). Genetic variations and patient-reported quality of life among patients with lung cancer. Journal of Clinical Oncology, 30, 1–9.
23.
go back to reference Clement, K., & Langin, D. (2007). Regulation of inflammation-related genes in human adipose tissue. Journal of Internal Medicine, 262(4), 422–430.PubMed Clement, K., & Langin, D. (2007). Regulation of inflammation-related genes in human adipose tissue. Journal of Internal Medicine, 262(4), 422–430.PubMed
24.
go back to reference Peters, M. J., Broer, L., Willemen, H. L., Eiriksdottir, G., Hocking, L. J., Holliday, K. L., et al. (2013). Genome-wide association study meta-analysis of chronic widespread pain: Evidence for involvement of the 5p15.2 region. Annals of Rheumatic Diseases, 72, 427–436. Peters, M. J., Broer, L., Willemen, H. L., Eiriksdottir, G., Hocking, L. J., Holliday, K. L., et al. (2013). Genome-wide association study meta-analysis of chronic widespread pain: Evidence for involvement of the 5p15.2 region. Annals of Rheumatic Diseases, 72, 427–436.
25.
go back to reference Nishizawa, D., Fukuda, K., Kasai, S., Hasegawa, J., Aoki, Y., Nishi, A., et al. (2014). Genome-wide association study identifies a potent locus associated with human opioid sensitivity. Molecular Psychiatry, 19(1), 55–62.PubMedCentralPubMed Nishizawa, D., Fukuda, K., Kasai, S., Hasegawa, J., Aoki, Y., Nishi, A., et al. (2014). Genome-wide association study identifies a potent locus associated with human opioid sensitivity. Molecular Psychiatry, 19(1), 55–62.PubMedCentralPubMed
26.
go back to reference Ingle, J. N., Schaid, D. J., Goss, P. E., Liu, M., Mushiroda, T., Chapman, J. A., et al. (2010). Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors. Journal of Clinical Oncology, 28, 4674–4682.PubMedCentralPubMed Ingle, J. N., Schaid, D. J., Goss, P. E., Liu, M., Mushiroda, T., Chapman, J. A., et al. (2010). Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors. Journal of Clinical Oncology, 28, 4674–4682.PubMedCentralPubMed
27.
go back to reference Galvan, A., Skorpen, F., Klepstad, P., Knudsen, A. K., Fladvad, T., Falvella, F. S., et al. (2011). Multiple loci modulate opioid therapy response for cancer pain. Clinical Cancer Research, 17, 4581–4587.PubMed Galvan, A., Skorpen, F., Klepstad, P., Knudsen, A. K., Fladvad, T., Falvella, F. S., et al. (2011). Multiple loci modulate opioid therapy response for cancer pain. Clinical Cancer Research, 17, 4581–4587.PubMed
28.
go back to reference van Meurs, J. B., Uitterlinden, A. G., Stolk, L., Kerkhof, H. J., Hofman, A., Pols, H. A., et al. (2009). A functional polymorphism in the catechol-O-methyltransferase gene is associated with osteoarthritis-related pain. Arthritis and Rheumatism, 60, 628–629.PubMed van Meurs, J. B., Uitterlinden, A. G., Stolk, L., Kerkhof, H. J., Hofman, A., Pols, H. A., et al. (2009). A functional polymorphism in the catechol-O-methyltransferase gene is associated with osteoarthritis-related pain. Arthritis and Rheumatism, 60, 628–629.PubMed
29.
go back to reference Fernandez-de-Las-Penas, C., Fernandez-Lao, C., Cantarero-Villanueva, I., Ambite-Quesada, S., Rivas-Martinez, I., Del Moral-Avila, R., et al. (2012). Catechol-O-methyltransferase genotype (Val158met) modulates cancer-related fatigue and pain sensitivity in breast cancer survivors. Breast Cancer Research and Treatment, 133, 405–412.PubMed Fernandez-de-Las-Penas, C., Fernandez-Lao, C., Cantarero-Villanueva, I., Ambite-Quesada, S., Rivas-Martinez, I., Del Moral-Avila, R., et al. (2012). Catechol-O-methyltransferase genotype (Val158met) modulates cancer-related fatigue and pain sensitivity in breast cancer survivors. Breast Cancer Research and Treatment, 133, 405–412.PubMed
30.
go back to reference Fijal, B., Perlis, R. H., Heinloth, A. N., & Houston, J. P. (2010). The association of single nucleotide polymorphisms in the catechol-O-methyltransferase gene and pain scores in female patients with major depressive disorder. Journal of Pain, 11(910–5), 915. Fijal, B., Perlis, R. H., Heinloth, A. N., & Houston, J. P. (2010). The association of single nucleotide polymorphisms in the catechol-O-methyltransferase gene and pain scores in female patients with major depressive disorder. Journal of Pain, 11(910–5), 915.
31.
go back to reference Finan, P. H., Zautra, A. J., Davis, M. C., Lemery-Chalfant, K., Covault, J., & Tennen, H. (2010). Genetic influences on the dynamics of pain and affect in fibromyalgia. Health Psychology, 29, 134–142.PubMedCentralPubMed Finan, P. H., Zautra, A. J., Davis, M. C., Lemery-Chalfant, K., Covault, J., & Tennen, H. (2010). Genetic influences on the dynamics of pain and affect in fibromyalgia. Health Psychology, 29, 134–142.PubMedCentralPubMed
32.
go back to reference Lindstedt, F., Karshikoff, B., Schalling, M., Olgart, H. C., Ingvar, M., Lekander, M., et al. (2012). Serotonin-1A receptor polymorphism (rs6295) associated with thermal pain perception. PLoS ONE, 7, e43221.PubMedCentralPubMed Lindstedt, F., Karshikoff, B., Schalling, M., Olgart, H. C., Ingvar, M., Lekander, M., et al. (2012). Serotonin-1A receptor polymorphism (rs6295) associated with thermal pain perception. PLoS ONE, 7, e43221.PubMedCentralPubMed
33.
go back to reference Lindstedt, F., Lonsdorf, T. B., Schalling, M., Kosek, E., & Ingvar, M. (2011). Perception of thermal pain and the thermal grill illusion is associated with polymorphisms in the serotonin transporter gene. PLoS ONE, 6, e17752.PubMedCentralPubMed Lindstedt, F., Lonsdorf, T. B., Schalling, M., Kosek, E., & Ingvar, M. (2011). Perception of thermal pain and the thermal grill illusion is associated with polymorphisms in the serotonin transporter gene. PLoS ONE, 6, e17752.PubMedCentralPubMed
34.
go back to reference Ortega-Hernandez, O. D., Cuccia, M., Bozzini, S., Bassi, N., Moscavitch, S., Diaz-Gallo, L. M., et al. (2009). Autoantibodies, polymorphisms in the serotonin pathway, and human leukocyte antigen class II alleles in chronic fatigue syndrome: Are they associated with age at onset and specific symptoms? Annals of New York Academy of Science, 1173, 589–599. Ortega-Hernandez, O. D., Cuccia, M., Bozzini, S., Bassi, N., Moscavitch, S., Diaz-Gallo, L. M., et al. (2009). Autoantibodies, polymorphisms in the serotonin pathway, and human leukocyte antigen class II alleles in chronic fatigue syndrome: Are they associated with age at onset and specific symptoms? Annals of New York Academy of Science, 1173, 589–599.
35.
go back to reference Olsen, M. B., Jacobsen, L. M., Schistad, E. I., Pedersen, L. M., Rygh, L. J., Roe, C., et al. (2012). Pain intensity the first year after lumbar disc herniation is associated with the A118G polymorphism in the opioid receptor mu 1 gene: Evidence of a sex and genotype interaction. Journal of Neuroscience, 32, 9831–9834.PubMed Olsen, M. B., Jacobsen, L. M., Schistad, E. I., Pedersen, L. M., Rygh, L. J., Roe, C., et al. (2012). Pain intensity the first year after lumbar disc herniation is associated with the A118G polymorphism in the opioid receptor mu 1 gene: Evidence of a sex and genotype interaction. Journal of Neuroscience, 32, 9831–9834.PubMed
36.
go back to reference Reimann, F., Cox, J. J., Belfer, I., Diatchenko, L., Zaykin, D. V., McHale, D. P., et al. (2010). Pain perception is altered by a nucleotide polymorphism in SCN9A. Proceedings of the National Academy of Science of the United States of America, 107, 5148–5153. Reimann, F., Cox, J. J., Belfer, I., Diatchenko, L., Zaykin, D. V., McHale, D. P., et al. (2010). Pain perception is altered by a nucleotide polymorphism in SCN9A. Proceedings of the National Academy of Science of the United States of America, 107, 5148–5153.
37.
go back to reference Sullivan, P. F., de Geus, E. J. C., Willemsen, G., James, M. R., Smit, J. H., Zandbelt, T., et al. (2009). Genomewide association for major depressive disorder: A possible role for the presynaptic protein piccolo. Molecular Psychiatry, 14(4), 359–375.PubMedCentralPubMed Sullivan, P. F., de Geus, E. J. C., Willemsen, G., James, M. R., Smit, J. H., Zandbelt, T., et al. (2009). Genomewide association for major depressive disorder: A possible role for the presynaptic protein piccolo. Molecular Psychiatry, 14(4), 359–375.PubMedCentralPubMed
38.
go back to reference Muglia, P., Tozzi, F., Galway, N. W., Francks, C., Upmanyu, R., Kong, X. Q., et al. (2010). Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts. Molecular Psychiatry, 15, 589–601.PubMed Muglia, P., Tozzi, F., Galway, N. W., Francks, C., Upmanyu, R., Kong, X. Q., et al. (2010). Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts. Molecular Psychiatry, 15, 589–601.PubMed
39.
go back to reference Shyn, S. I., Shi, J., Kraft, J., Potash, J., Knowles, J. A., Weismann, M. M., et al. (2011). Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. Molecular Psychiatry, 16(2), 202–215.PubMedCentralPubMed Shyn, S. I., Shi, J., Kraft, J., Potash, J., Knowles, J. A., Weismann, M. M., et al. (2011). Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. Molecular Psychiatry, 16(2), 202–215.PubMedCentralPubMed
40.
go back to reference Hek, K., Demirkan, A., Lahti, J., Terracciano, A., Teumer, A., & Cornelis, M. C. (2012). A genome-wide association study of depressive symptoms. Biological Psychiatry, 73, 667–678. Hek, K., Demirkan, A., Lahti, J., Terracciano, A., Teumer, A., & Cornelis, M. C. (2012). A genome-wide association study of depressive symptoms. Biological Psychiatry, 73, 667–678.
41.
go back to reference Kao, C.-F., Fang, Y.-S., Zhao, Z., & Kuo, P.-H. (2011). Prioritization and evaluation of depression candidate genes by combining multidimensional data resources. PLoS ONE, 6(4), e18696.PubMedCentralPubMed Kao, C.-F., Fang, Y.-S., Zhao, Z., & Kuo, P.-H. (2011). Prioritization and evaluation of depression candidate genes by combining multidimensional data resources. PLoS ONE, 6(4), e18696.PubMedCentralPubMed
42.
go back to reference Bao, A.-M., Meynena, G., & Swaaba, D. F. (2008). The stress system in depression and neurodegeneration: Focus on the human hypothalamus. Brain Research Reviews, 57(2), 531–553.PubMed Bao, A.-M., Meynena, G., & Swaaba, D. F. (2008). The stress system in depression and neurodegeneration: Focus on the human hypothalamus. Brain Research Reviews, 57(2), 531–553.PubMed
43.
go back to reference Dowlati, Y., Herrmann, N., Swardfager, W., Liu, H., Sham, L., Reim, E. K., et al. (2010). A meta-analysis of cytokines in major depression. Biological Psychiatry, 67, 446–457.PubMed Dowlati, Y., Herrmann, N., Swardfager, W., Liu, H., Sham, L., Reim, E. K., et al. (2010). A meta-analysis of cytokines in major depression. Biological Psychiatry, 67, 446–457.PubMed
44.
go back to reference Illi, J., Miaskowski, C., Cooper, B., Levine, J. D., Dunn, L., West, C., et al. (2012). Association between pro- and anti-inflammatory cytokine genes and a symptom cluster of pain, fatigue, sleep disturbance, and depression. Cytokine, 58, 437–447.PubMedCentralPubMed Illi, J., Miaskowski, C., Cooper, B., Levine, J. D., Dunn, L., West, C., et al. (2012). Association between pro- and anti-inflammatory cytokine genes and a symptom cluster of pain, fatigue, sleep disturbance, and depression. Cytokine, 58, 437–447.PubMedCentralPubMed
45.
go back to reference Bower, J. E., Ganz, P. A., Irwin, M. R., Castellon, S., Arevalo, J., & Cole, S. W. (2013). Cytokine genetic variations and fatigue among patients with breast cancer. Journal of Clinical Oncology, 31(13), 1656–1661.PubMedCentralPubMed Bower, J. E., Ganz, P. A., Irwin, M. R., Castellon, S., Arevalo, J., & Cole, S. W. (2013). Cytokine genetic variations and fatigue among patients with breast cancer. Journal of Clinical Oncology, 31(13), 1656–1661.PubMedCentralPubMed
46.
go back to reference Piraino, B., Vollmer-Conna, U., & Lloyd, A. R. (2012). Genetic associations of fatigue and other symptom domains of the acute sickness response to infection. Brain, Behavior, and Immunity, 26, 552–558.PubMed Piraino, B., Vollmer-Conna, U., & Lloyd, A. R. (2012). Genetic associations of fatigue and other symptom domains of the acute sickness response to infection. Brain, Behavior, and Immunity, 26, 552–558.PubMed
47.
go back to reference Holtzman, S., Abbey, S. E., Chan, C., Bargman, J. M., & Stewart, D. E. (2012). A genetic predisposition to produce low levels of IL-10 is related to depressive symptoms: A pilot study of patients with end stage renal disease. Psychosomatics, 53, 155–161.PubMed Holtzman, S., Abbey, S. E., Chan, C., Bargman, J. M., & Stewart, D. E. (2012). A genetic predisposition to produce low levels of IL-10 is related to depressive symptoms: A pilot study of patients with end stage renal disease. Psychosomatics, 53, 155–161.PubMed
48.
go back to reference De Neve, J. E. (2011). Functional polymorphism (5-HTTLPR) in the serotonin transporter gene is associated with subjective well-being: Evidence from a US nationally representative sample. Journal of Human Genetics, 56(6), 456–459.PubMed De Neve, J. E. (2011). Functional polymorphism (5-HTTLPR) in the serotonin transporter gene is associated with subjective well-being: Evidence from a US nationally representative sample. Journal of Human Genetics, 56(6), 456–459.PubMed
49.
go back to reference De Neve, J. E., Christakis, N. A., Fowler, J. H., & Frey, B. S. (2012). Genes, economics, and happiness. Journal of Neuroscience, Psychology, and Economics, 5(4), 193–211. De Neve, J. E., Christakis, N. A., Fowler, J. H., & Frey, B. S. (2012). Genes, economics, and happiness. Journal of Neuroscience, Psychology, and Economics, 5(4), 193–211.
50.
go back to reference Chen, H., Pine, D. S., Ernst, M., Gorodetsky, E., Kasen, S., Gordon, K., et al. (2013). The MAOA gene predicts happiness in women. Progress in Neuropsychopharmacology and Biological Psychiatry, 10(40), 122–125. Chen, H., Pine, D. S., Ernst, M., Gorodetsky, E., Kasen, S., Gordon, K., et al. (2013). The MAOA gene predicts happiness in women. Progress in Neuropsychopharmacology and Biological Psychiatry, 10(40), 122–125.
51.
go back to reference Rietveld, C. A., Cesarini, D., Benjamin, D. J., Koellinger, P. D., De Neve, J. E., Tiemeier, H., et al. (2013). Molecular genetics and subjective well-being. Proceedings of the National Academy of Sciences of the United States of America, 110(24), 9692–9697.PubMedCentralPubMed Rietveld, C. A., Cesarini, D., Benjamin, D. J., Koellinger, P. D., De Neve, J. E., Tiemeier, H., et al. (2013). Molecular genetics and subjective well-being. Proceedings of the National Academy of Sciences of the United States of America, 110(24), 9692–9697.PubMedCentralPubMed
52.
go back to reference Holmes, A. J., Lee, P. H., Hollinshead, M. O., Bakst, L., Roffman, J. L., Smoller, J. W., et al. (2012). Individual differences in amygdala-medial prefrontal anatomy link negative affect, impaired social functioning, and polygenic depression risk. Journal of Neuroscience, 32(50), 18087–18100.PubMedCentralPubMed Holmes, A. J., Lee, P. H., Hollinshead, M. O., Bakst, L., Roffman, J. L., Smoller, J. W., et al. (2012). Individual differences in amygdala-medial prefrontal anatomy link negative affect, impaired social functioning, and polygenic depression risk. Journal of Neuroscience, 32(50), 18087–18100.PubMedCentralPubMed
53.
go back to reference Antypa, N., Calati, R., Souery, D., Pellegrini, S., Sentissi, O., Amital, D., et al. (2013). Variation in the HTR1A and HTR2A genes and social adjustment in depressed patients. Journal of Affective Disorders, 150(2), 649–652.PubMed Antypa, N., Calati, R., Souery, D., Pellegrini, S., Sentissi, O., Amital, D., et al. (2013). Variation in the HTR1A and HTR2A genes and social adjustment in depressed patients. Journal of Affective Disorders, 150(2), 649–652.PubMed
54.
go back to reference Brown, A. A., Jensen, J., Nikolova, Y. S., Djurovic, S., Agartz, I., Server, A., et al. (2012). Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach. Translational Psychiatry, 2, e143.PubMedCentralPubMed Brown, A. A., Jensen, J., Nikolova, Y. S., Djurovic, S., Agartz, I., Server, A., et al. (2012). Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach. Translational Psychiatry, 2, e143.PubMedCentralPubMed
55.
go back to reference Vinkhuyzen, A. A., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K., Iacono, W. G., et al. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry, 2, e102.PubMedCentralPubMed Vinkhuyzen, A. A., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K., Iacono, W. G., et al. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry, 2, e102.PubMedCentralPubMed
56.
go back to reference Kim, H. N., Roh, S. J., Sung, Y. A., Chung, H. W., Lee, J. Y., Cho, J., et al. (2013). Genome-wide association study of the five-factor model of personality in young Korean women. Journal of Human Genetics, 58(10), 667–674.PubMed Kim, H. N., Roh, S. J., Sung, Y. A., Chung, H. W., Lee, J. Y., Cho, J., et al. (2013). Genome-wide association study of the five-factor model of personality in young Korean women. Journal of Human Genetics, 58(10), 667–674.PubMed
57.
go back to reference Luciano, M., Huffman, J. E., Arias-Vasquez, A., Vinkhuyzen, A. A., Middeldorp, C. M., Giegling, I., et al. (2012). Genome-wide association uncovers shared genetic effects among personality traits and mood states. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B(6), 684–695. Luciano, M., Huffman, J. E., Arias-Vasquez, A., Vinkhuyzen, A. A., Middeldorp, C. M., Giegling, I., et al. (2012). Genome-wide association uncovers shared genetic effects among personality traits and mood states. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B(6), 684–695.
58.
go back to reference Amin, N., Hottenga, J. J., Hansell, N. K., Janssens, A. C., de Moor, M. H., Madden, P. A., et al. (2013). Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. European Journal of Human Genetics, 21(8), 876–882.PubMedCentralPubMed Amin, N., Hottenga, J. J., Hansell, N. K., Janssens, A. C., de Moor, M. H., Madden, P. A., et al. (2013). Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. European Journal of Human Genetics, 21(8), 876–882.PubMedCentralPubMed
59.
go back to reference Lucas-Thompson, R. G., & Holman, E. A. (2013). Environmental stress, oxytocin receptor gene (OXTR) polymorphism, and mental health following collective stress. Hormones and Behavior, 63(4), 615–624.PubMed Lucas-Thompson, R. G., & Holman, E. A. (2013). Environmental stress, oxytocin receptor gene (OXTR) polymorphism, and mental health following collective stress. Hormones and Behavior, 63(4), 615–624.PubMed
60.
go back to reference Montag, C., Brockmann, E. M., Lehmann, A., Muller, D. J., Rujescu, D., & Gallinat, J. (2012). Association between oxytocin receptor gene polymorphisms and self-rated ‘empathic concern’ in schizophrenia. PLoS ONE, 7(12), e51882.PubMedCentralPubMed Montag, C., Brockmann, E. M., Lehmann, A., Muller, D. J., Rujescu, D., & Gallinat, J. (2012). Association between oxytocin receptor gene polymorphisms and self-rated ‘empathic concern’ in schizophrenia. PLoS ONE, 7(12), e51882.PubMedCentralPubMed
61.
go back to reference Norman, G. J., Hawkley, L., Luhmann, M., Ball, A. B., Cole, S. W., Berntson, G. G., et al. (2012). Variation in the oxytocin receptor gene influences neurocardiac reactivity to social stress and HPA function: A population based study. Hormones and Behavior, 61(1), 134–139.PubMed Norman, G. J., Hawkley, L., Luhmann, M., Ball, A. B., Cole, S. W., Berntson, G. G., et al. (2012). Variation in the oxytocin receptor gene influences neurocardiac reactivity to social stress and HPA function: A population based study. Hormones and Behavior, 61(1), 134–139.PubMed
62.
go back to reference Olff, M., Frijling, J. L., Kubzansky, L. D., Bradley, B., Ellenbogen, M. A., Cardoso, C., et al. (2013). The role of oxytocin in social bonding, stress regulation and mental health: An update on the moderating effects of context and interindividual differences. Psychoneuroendocrinology, 38(9), 1883–1894.PubMed Olff, M., Frijling, J. L., Kubzansky, L. D., Bradley, B., Ellenbogen, M. A., Cardoso, C., et al. (2013). The role of oxytocin in social bonding, stress regulation and mental health: An update on the moderating effects of context and interindividual differences. Psychoneuroendocrinology, 38(9), 1883–1894.PubMed
63.
go back to reference Kumsta, R., Hummel, E., Chen, F. S., & Heinrichs, M. (2013). Epigenetic regulation of the oxytocin receptor gene: Implications for behavioral neuroscience. Frontiers in Neuroscience, 7, 83.PubMedCentralPubMed Kumsta, R., Hummel, E., Chen, F. S., & Heinrichs, M. (2013). Epigenetic regulation of the oxytocin receptor gene: Implications for behavioral neuroscience. Frontiers in Neuroscience, 7, 83.PubMedCentralPubMed
64.
go back to reference Belsky, J., & Pluess, M. (2013). Genetic moderation of early child-care effects on social functioning across childhood: A developmental analysis. Child Development, 84(4), 1209–1225.PubMed Belsky, J., & Pluess, M. (2013). Genetic moderation of early child-care effects on social functioning across childhood: A developmental analysis. Child Development, 84(4), 1209–1225.PubMed
65.
go back to reference Fergusson, D. M., Boden, J. M., Horwood, L. J., Miller, A. L., & Kennedy, M. A. (2011). MAOA, abuse exposure and antisocial behaviour: 30-year longitudinal study. British Journal of Psychiatry, 198, 457–463.PubMedCentralPubMed Fergusson, D. M., Boden, J. M., Horwood, L. J., Miller, A. L., & Kennedy, M. A. (2011). MAOA, abuse exposure and antisocial behaviour: 30-year longitudinal study. British Journal of Psychiatry, 198, 457–463.PubMedCentralPubMed
66.
go back to reference Strohmaier, J., Amelang, M., Hothorn, L. A., Witt, S. H., Nieratschker, V., Gerhard, D., et al. (2013). The psychiatric vulnerability gene CACNA1C and its sex-specific relationship with personality traits, resilience factors and depressive symptoms in the general population. Molecular Psychiatry, 18(5), 607–613.PubMedCrossRef Strohmaier, J., Amelang, M., Hothorn, L. A., Witt, S. H., Nieratschker, V., Gerhard, D., et al. (2013). The psychiatric vulnerability gene CACNA1C and its sex-specific relationship with personality traits, resilience factors and depressive symptoms in the general population. Molecular Psychiatry, 18(5), 607–613.PubMedCrossRef
Metagegevens
Titel
Biological pathways, candidate genes, and molecular markers associated with quality-of-life domains: an update
Auteurs
Mirjam A. G. Sprangers
Melissa S. Y. Thong
Meike Bartels
Andrea Barsevick
Juan Ordoñana
Qiuling Shi
Xin Shelley Wang
Pål Klepstad
Eddy A. Wierenga
Jasvinder A. Singh
Jeff A. Sloan
Publicatiedatum
01-09-2014
Uitgeverij
Springer International Publishing
Gepubliceerd in
Quality of Life Research / Uitgave 7/2014
Print ISSN: 0962-9343
Elektronisch ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-014-0656-1

Andere artikelen Uitgave 7/2014

Quality of Life Research 7/2014 Naar de uitgave