Susceptibilidad genética y enfermedad autoinmune reumática: Revisión narrativa
DOI:
https://doi.org/10.36829/63CTS.v8i1.907Resumen
La autoinmunidad es la consecuencia de la pérdida de control y regulación de la respuesta inmune. Se reporta que ocurre entre 5 y 9% de patologías a nivel mundial. A las enfermedades con esta anomalía se les denomina autoinmunes y se clasifican de acuerdo con el órgano o sistema afectado. Las reumáticas involucran al tejido conectivo y las articulaciones. Los factores asociados a su aparición incluyen: edad, género, medioambiente y genéticos. La susceptibilidad genética indica la presencia de uno o varios genes asociados al desarrollo de determinada enfermedad, cuya expresión podría ser el producto de la migración, selección, recombinación y adaptación de genes entre las poblaciones, lo que explica la variación fenotípica y la expresión clínica resultante. Los estudios de asociación del genoma completo (GWAS por sus siglas en inglés) han permitido identificar múltiples genes involucrados con enfermedades reumáticas, destacan el lupus eritematoso sistémico y artritis reumatoide, asociadas con más de 60 alelos, y otras como la espondilitis anquilosante, en donde la asociación ha sido primordialmente con un gen y sus polimorfismos. Esta revisión tiene como objetivo informar el estado de la susceptibilidad determinada genéticamente para estas enfermedades y el impacto que tiene sobre la expresión clínica. Se realizó una búsqueda en PubMed y la base de datos de la biblioteca Cochrane, se incluyeron artículos relacionados con las palabras clave propuestas desde el 2000. La revisión identifica genes y la asociación con estas enfermedades, expone la diversidad existente y justifica continuar la búsqueda de genes en todas las poblaciones.
Descargas
Citas
Alarcón-Riquelme, M. E., Ziegler, J., Molineros, J., Howard, T.D., Moreno-Estrada, A., Sánchez- Rodríguez, E., Ainsworth, H., Ortíz-Tello, P., Comeau, M., Rasmussen, A., Kelly, J., Adler, A., Acevedo-Vásquez, E., Cucho-Venegas, J., García-De la Torre, I., Cardiel, M., Miranda, P., Catoggio, L., Maradiaga-Ceceña, M., Gaffney, P., … Jacob, C. (2016). GWAS in an Amerindian ancestry population reveals novel systemic lupus erythematosus risk loci and the role of European admixture. Arthritis & Rheumatology, 68(4), 932-943. https://doi.org/10.1002/art.39504
Alarcón-Segovia, D., Alarcón-Riquelme, M. E., Cardiel, M. H., Caeiro, F., Massardo, L., Villa, A.R., Pons-Estel, B., & Grupo Latinoamericano de Estudio del Lupus Eritematoso (GLADEL) (2005). Familial aggregation of systemic lupus erythematosus, rheumatoid arthritis, and other autoimmune diseases in 1,177 lupus patients from the GLADEL cohort. Arthritis & Rheumatology, 52(4), 1138-1147. https://doi.org/10.1002/art.20999
Asquith, M., Sternes, P., Costello, ME., Karstens, L., Diamond, S., Martin, T., Li, Z., Marshall, M., Spector, T., Cao, K., Rosenbaum, J., & Brown, M. (2019). HLA Alleles Associated with Risk of Ankylosing Spondylitis and Rheumatoid Arthritis Influence the Gut Microbiome. Arthritis & Rheumatology, 71(10), 1642-1650. https://doi.org/10.1002/art.40917
Baños, C., & Muñoz-Valle, J. (2017). PADI4 polymorphisms and the functional haplotype are associated with increased rheumatoid arthritis susceptibility: A replication study in a Southern Mexican population. Human Immunology, 78, 553-558. https://doi.org/10.1016/j.humimm.2017.05.005
Barturen, G., & Alarcón-Riquelme, M. E. (2018). Moving towards a molecular taxonomy of autoimmune rheumatic diseases. Nature Reviews Rheumatology, 14, 75-93. https://doi.org/10.1038/nrrheum.2017.220
Bax, M., Van Heernst, J., Huizinga, T. W., & Toes, R. E. (2011). Genetics of rheumatoid arthritis: what have we learned? Immunogenetics 63, 459-466. https://doi.org/10.1007/s00251-011-0528-6
Belsky D., & Israel S. (2014). Integrating Genetics and Social Science: Genetic Risk Scores. Biodemography and Social Biology, 60, 137-155. https://doi.org/10.1080/19485565.2014.946591
Bentham J., Morris D. L., Graham, D. S. C., Pinder, C. L., Tombleson P., Behrens T. W. Martin, J., Fairfax, B., Knight, J., Chen, L., Replogle, J., Syvänen, A., Rönnblom, L., Graham, R., Wither, J., Rioux, J., Alarcón-Riquelme, M. E., & Vyse, T.J. (2015). Genetic association analyses implicate aberrant regulation of innate and adaptative immunity genes in the pathogenesis of systemic lupus erythematosus. Nature Genetic, 47, 1457-1464. https://doi.org/10.1038/ng.3434
Burton, P., Clayton, D., Cardon, L., & Wellcome Trust Case Control Consortium Australo- Anglo-American Spondylitis Consortium (TASC) (2007). Association scan of 14,500 nonsynonymus SNPs in four diseases identifies autoimmunity variants. Nature Genetics, 39(11), 1329-1337. https://doi.org/10.1038/ng.2007.17
Castaño-Rodríguez, N., Diaz-Gallo, L. M., Pineda- Tamayo, R., Rojas-Villarraga, A., & Anaya, J. M. (2008). Meta-analysis of HLA-DRB1 and HLA-DQB1 polymorphisms in Latin American patients with systemic lupus erythematosus. Autoimmunity Reviws, 7, 322-330. https://doi.org/10.1016/j.autrev.2007.12.002
Castro-Santos, P., & Díaz-Peña, R. (2016). Genetics of rheumatoid arthritis: a new boost is needed in Latin American populations. Revista Brasileira de Reumatología, 56(2), 171-177. https://doi.org/10.1016/j.rbre.2015.10.004
Carlton, V. E. H., Xu, H., Chokkalingam, A. P., Schrodi, S. J., Brandon, R., Alexander, H. C., Chang, M., Catanese, J., Leong, D., Ardlie, K., Kastner, D., Seldin, M., Criswell, L., Gregersen, P., Beasley, E., Thomson, G., Amos, C., & Begovich, A.B. (2005). PTPN22 Genetic variation: Evidence for multiple variants associated with rheumatoid arthritis. American Journal of Human Genetics, 77, 567-581. https://doi.org/10.1086/468189
Connolly, J., & Hakonarson, H. (2012). Role de cytokines in systemic lupus erythematosus: recent progress from GWAS and sequencing. Journal of Biomedicine and Biotechnology, 2012, 798924. https://doi.org/10.1155/2012/798924
Crow, M., (2008). Collaboration, genetic associations, and lupus erythematosus. New England Journal of Medicine, 358, 956-961. https://doi.org/10.1056/NEJMe0800096
David, T., Ling, S., & Barton, A. (2018). Genetics of immune-mediated inflammatory diseases. Clinical and Experimental Immunology, 193, 3-12. https://doi.org/10.1111/cei.13101
Deane, K., & Carlson, E. (2012). Environmental and gene-environment interactions and risk of rheumatoid arthritis. Rheumatic Diseases Clinics of North American, 38(2), 405-426. https://doi.org/10.1016/j.rdc.2012.04.002
De la Calle-Fabregat, C., Morante-Palacios, O., & Ballestar, E. (2020). Understanding the relevance of DNA methylation changes in immune differentiation and disease. Genes, 11(1), 110. https://doi.org/10.3390/genes11010110
Delgado-Vega, A. M, & Anaya, J. M. (2007). Meta- analysis of HLA-DRB1 polymorphism in Latin American patients with rheumatoid arthritis. Autoimmunity Reviews, 6, 402-408. https://doi.org/10.1016/j.autrev.2006.11.004
Ebrahimiyan, H., Mostafae, S., Aslani, S., Jamshidi, A., & Mahmoudi, M. (2019). Studying the association between STAT4 gene polymorphism and susceptibility to rheumatoid arthritis disease: An updated meta-analysis. Iranian Journal of Immunology, 16(19),71-83. https://doi. org/10.22034/IJI.2019.39408
Eyre, S., Orozco, G., & Worthington, J. (2017). The genetics revolution in rheumatology: large scale genomic arrays and genetic mapping. Nature Reviews Rheumatology, 13, 421-432. https://doi.org/10.1038/nrrheum.2017.80
Fernando, M. M. A., Stevens, C. R., Walsh, E. C., De Jager, P. L., Goyette, P., Plenge, R. M. Vyse, T., & Riux, J. D. (2008). Defining the role of the MHC in autoimmunity: a reviewed and pooled analysis. PLoS Genetics, 4(4). https://doi.org/10.1371/journal.pgen.1000024
Furukawa, H., Oka, S., Kawasaki, A., Hidaka, M., Shimada, K., Kondo, Y., Ihata, A., Matsushita, T., Matsumoto, T., Komiya, A., Kobayashi, K., Osada, A., Katayama, M., Okamoto, A., Setoguchi, K., Kono, H., Hamaguchi, Y., Matsui, T., Fukui, N., Tamura, H., … Thoma, S. (2020). Human leukocyte antigen in Japanese patients with idiopathic inflammatory myopathy. Modern Rheumatology, 30(4), 696-702. https://doi.org/10.1080/14397595.2019.1637593
Godkhe-Puranik, Y., & Niewold, T. (2015).Immunogenetics of systemic lupus erythematosus: A comprehensive review. Journal of Autoimmunity, 64, 125-136. https://doi.org/10.1016/j.jaut.2015.08.004
Graham, R. R., Kyogoku, C., Sigurdsson, S., Vlasova, I. A., Davies, L. R. L., Baechler, E. C., Plenge, R., Koeuth, T., Ortmann, W., Hom, G., Bauer, J., Gillett, C., Burtt, N., Cunninghame, D., Onofrio, R., Petri, M., Gunnarsson, I., Svenungsson, E., Rönnblom, L., Nordmark D., … Altshuler D. (2007). Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus. Proceedings of the National Academy of Sciences of the United States of America, 104, 6758-6763.
https://doi.org/10.1073/pnas.0701266104
Hanson, A., & Brown, M. (2017). Genetics and the causes of ankylosing spondylitis. Rheumatic Diseases Clinics of North American, 43, 401-414. https://doi.org/10.1016/j.rdc.2017.04.006
Harley, J., Alarcón-Riquelme, M. E., Criswell, L., Jacob, C., Kimberly R., & Moser, K. (2008). Genome wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci. Nature Genetics, 40, 204-210. https://doi.org/10.1038/ng.81
Hiraki, L., & Silverman, E. (2017). Genomics of systemic lupus erythematosus: Insights Gained by studying monogenic young onset. Rheumatic Diseases Clinics of North American, 43, 415-434. https://doi.org/10.1016/j.rdc.2017.04.005
Hom, G., Graham, R. R., Modrek, B., Taylor, K. E., Ortmann, W., Garnier, S., Lee, A., Chung, S., Ferreira, R., Pant, K., Ballinger, D., Kosoy, R., Demirci, Y., Ilyas, M., Kao, A., Tian, C., Gunnarsson, I., Bengtsson, A., Rantapää- Dahlqvist, S., Petri, M., … Behrens T.W. (2008). Association of systemic lupus erythematosus with C8orf13-BLK and ITGAMITGAX. New England Journal of Medicine, 358, 900-909. https://doi.org/10.1056/NEJMoa0707865
Javinani, A., Ashraf-Ganjouei, A., Aslani, S., Jamshidi, A., & Mahmoudi, M. (2019). Exploring the etiopathogenesis of systemic lupus erythematosus: a genetic perspective. Immunogenetics, 71(4), 283-297. https://doi.org/10.1007/s00251-019-01103-2
Kamitaki, N., Sekar, A., Handsaker, R., de Rivera, H., Tooley, K., Morris, D.L., Taylor, K., Whelan, C., Tombleson, P., Olde, L., Boehnke, M., Kimberly, R., Kaufman, K., Harley, J., Langefeld, C., Seidman, C., Pato, M., Pato, C., Ophoff, R., Graham, R., … McCarroll, S. A. (2020). Complement genes contribute sex-biased vulnerability in diverse disorders. Nature, 582, 577.581. https://doi.org/10.1038/s41586-020-2277-x
Karami, J., Aslani, S., Jamshidi, A., Garhasbi M., & Mahmoudi, M. (2019). Genetic implication in the pathogenesis of rheumatoid arthritis; an updated review. Gene, 702, 8-16. https://doi.org/10.1016/j.gene.2019.03.033
Kim, K., Bang, S.-Y., Hyun Yoo, D., Cho, S.-K., Choi, C.-B., Sung, Y.-K., Kim, T.-H., Jun, J.-B., Kang, Y., Suh, C.-H., Shim, S.-C., Lee, S.-S., Lee, J., Chung, W., Kim, S.-K., Choe, J.-Y., Nath, S., Lee, H.-S., & Bae, S.-C. (2016). Imputing variants in HLA-DR beta genes reveals that HLA-DRB1 is solely associated with rheumatoid arthritis and systemic lupus erythematosus. PLoS ONE, 11(2), e0150283. https://doi.org/10.1371/journal.pone.0150283
Klareskog, L., Padyukov, L., Lorentzen, J., & Alfredsson, L. (2006). Mechanisms of disease: genetic susceptibility and environmental triggers in the development of rheumatoid arthritis. Nature Review Rheumatology, 2, 425-433. https://doi.org/10.1038/ncprheum0249
Kozyrev, S., Abelson, A., Wojcik, J., Zaghlool, A., Linga, M., Sánchez, E., Gunnarsson, I., Svenungsson, E., Sturfelt, G., Jönsen, A., Truedsson, L., Pons-Estel, B., Witte, T., D'Alfonso, S., Barizzone, N., Danieli, M.-G., Gutierrez, C., Suarez, A., Junker, P., Laustrup, H., … Alarcón-Riquelme, M. E. (2008). Functional variants in the B cell gene BANK1 are associated with systemic lupus erythematosus. Nature Genetics, 40, 211-216. https://doi.org/10.1038/ng.79
Kuo, C.-F., Grainge, M., Valdes, A., See, L.-C., Yu, K.-H., Shaw, S., Lou, S.-F., Zhang, W., & Doherty, M. (2017). Familial aggregation of rheumatoid arthritis and co-aggregation of autoimmune diseases in affected families: a nationwide population-based study. Rheumatology, 56, 928-933. https://doi.org/10.1093/rheumatology/kew500
Langefeld, C.D., Ainsworth, H., Cunninghame, D., Kelly, J., Comeau, M., Marion, M., Howard, T., Ramos, P., Croker, J., Morris, D., Sandling, J., Carlsson, J., Acevedo-Vásquez, E., Alarcón, G., Babini, A., Baca, V., Bengtsson, A., De la Rúa Figueroa, I., Doria, A., Edberg, J., … Vyse, T. (2017). Transancestral mapping and genetic load in systemic lupus erythematosus. Natural Communications, 8, 16021. https://doi.org/10.1038/ncomms16021
Laufer, V., Chen, J., Langefeld, C., & Bridges, L. (2017). Integrative approaches to understanding the pathogenic role of genetic variation in rheumatic diseases. Rheumatic Diseases Clinics of North American, 43(3), 449-466. https://doi.org/10.1016/j.rdc.2017.04.012
López Herráez, D., Martínez-Bueno, M., García de la Torre, I., Sacnún, M., & Goñi, M. (2013). Rheumatoid arthritis in Latin Americans enriched for Amerindian ancestry is associated with loci in chromosomes 1, 12 and 13, and the HLA class II region. Arthritis & Rheumatology, 65(6), 1457-1467. https://doi.org/10.1002/art.37923
Matzaraki, V., Kumar, V., Wijmenga, C., & Zhernakova, A. (2017). The MHC locus and genetic susceptibility to autoimmune and infectious diseases. Genome Biology, 18, 76, 2-21. https://doi.org/10.1186/s13059-017-1207-1
Morris. D., Taylor, K., Fernando, M., Nititham, J., Alarcón-Riquelme, M. E., Barcellos, L., Behrens, T., Cotsapas, C., Gaffney, P., Graham, R., Pons- Estel, B., Gregersen, P., Harley, J., Hauser, S., Hom, G., Langefeld, G., Noble, J., International MHC and Autoimmunity Genetics Network & Vyse T. (2012). Unraveling multiple MHC gene associations with systemic lupus erythematosus: Model choice indicates a role for HLA alleles and non-HLA genes in Europeans. American Journal of Human Genetics 91, 778-793. https://doi.org/10.1016/j.ajhg.2012.08.026
Moser, K., Kelly, J., Lessard, C., & Harley, J. (2009). Recent insights into the genetic basis of systemic lupus erythematosus. Genes Immunology, 10, 373-379. https://doi.org/10.1038/gene.2009.39
Muñoz-Valle, J., Padilla-Gutiérrez, J., Hernández- Bello, J., Ruiz-Noa, Y., Valle, Y., Palafox- Sánchez, C., Parra-Rojas, I., Gutiérrez-Ureña, S., & Rangel-Villalobos, H. (2017). Polimorfismo-1123G>C en el gen PTPN22 y anticuerpos antipéptido citrulinado cíclico en la artritis reumatoide. Reumatología Clínica, 149(3), 95-100. https://doi.org/10.1016/j.medcli.2017.01.025
Nath, S., Han, S., Kim-Howard, X., Kelly, J., Viswanathan, P., Gilkeson, G., Chen, W., Zhu, C., McEver, R., Kimberly, R., Alarcón-Riquelme, M.-E., Vyse, T., Li, Q.-Z., Wakeland, E., Merrill, J., James, J., Kaufman, K., Guthridge, J., & Harley, J. (2008). A nonsynonymous functional variant in integrin-alpha (M) encoded by ITGAM is associated with systemic lupus erythematosus. Nature Genetics, 40, 152-154. https://doi.org/10.1038/ng.71
Niewold, T., Kelly, J., Kariuki, S., Franek, B., Kumar, A., Kaufman, K., Thomas, K., Walker, D., Kamp, S., Frost, J., Wong, G., Merrill, J., Alarcón- Riquelme, M.-E., Tikly, M., Ramsey-Goldman, R., Reveille, J., Petri, M., Edberg, J., Kimberly, P., Alarcón, G., … Harley, J. B. (2012). IRF5 haplotypes demonstrate diverse serological associations which predict serum interferon alpha activity and explain the majority of the genetic association with systemic lupus erythematosus. Annals of the Rheumatic Diseases, 71(3), 463-468. https://doi.org/10.1136/annrheumdis-2011-200463
Okada, Y., Kishikawa, T., Sakaue, S., & Hirata, J. (2017). Future directions of genomics in rheumatic diseases. Rheumatic Diseases Clinics of North American, 43(3), 481-487. https://doi.org/10.1016/j.rdc.2017.04.009
Okada, Y., Eyre, S., Suzuki, A., Kochi Y., & Yamamoto, K. (2018). Genetic of rheumatoid arthritis: 2018 status. Annals of Rheumatic Diseases, 78, 446-473. https://doi.org/10.1136/annrheumdis-2018-213678
Osgood, J. E., & Knight, J. C. (2018). Translating GWAS in rheumatic disease: approaches to establishing mechanism and function for genetic associations with ankylosing spondylitis. Briefing in Functional Genomics, 17(5), 308-318. https://doi.org/10.1093/bfgp/ely015
Pearson, T. A., & Manolio, T. A. (2008). How to interpret a genome wide association study. Journal American Medical Association, 299(11), 1335-1344. https://doi.org/10.1001/jama.299.11.1335
Ramos, P., Criswell, L. A., Moser, K. L., Comeau, M. E., Williams, A. H., Pajewski, N. M., Chung, S., Graham, R., Zidovetzki, R., Kelly, J., Kaufman, K., Jacob, C., Vyse, T., Tsao, B., Kimberly, R., Gaffney, P., Alarcón-Riquelme, M.-E., Harley, J., Langefeld, C., & International Consortium of the Genetics of Systemic Erythematosus Lupus (SLEGEN). (2011). A comprehensive analysis of shared loci between systemic lupus erythematosus and sixteen autoimmune diseases reveals limited genetic overlap. PLoS Genetics,7(12), e1002406. https://doi.org/10.1371/journal.pgen.1002406
Ramírez-Bello, J., Jiménez-Morales, S., Montufar- Robles, I., Fragoso, J., Barbosa-Cobos, R. E., Saavedra, M. A., & Sánchez-Muñoz, F. (2019). BLK and BANK1 polymorphisms and interactions are associated in Mexican patients with lupus erythematosus. Inf lammation Research, 68, 705-713. https://doi.org/10.1007/s00011-019-01253-9
Reid, S., Alexsson, A., Frodlund, M., Morris, D., Sandling, J. K., Bolin, K., Svenungsson, E., Jönsen, A., Bengtsson, C., Gunnarsson, I., Illescas Rodriguez, V., Bengtsson, A., Arve, S., Rantapää-Dahlqvist, S., Eloranta, M.-L., Syvänen, A.-C., Sjöwall, C., Vyse, T., Rönnblom, R., & Leonard, D. (2020). High genetic risk score is associated with early disease onset, damage accrual and decreased survival in systemic lupus erythematosus. Annals of Rheumatic Diseases, 79, 363-369. https://doi.org/10.1136/annrheumdis-2019-216227
Reksten, T. R., Lessard, C. J., & Sivils, K. L. (2016). Genetics in Sjögren syndrome. Rheumatic Diseases Clinics of North American, 42, 435-447. https://doi.org/10.1016/j.rdc.2016.03.003
Reveille, J., Sims, A., Danoy, P., Evans, D., Leo, P., Pointon, L., Jin, R., Zhou, X., Bradbury, L., Appleton, L., Davis, J., Diekman, L., Doan, T., Dowling, A., Duan, R., Duncan, E., Farrar, C., Hadler, J., Harvey, D., Karaderi, T., … Brown, M. [The Australo-Anglo-American Spondyloarthritis Consortium (TASC)]. (2010). Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. Nature Genetics, 42(2), 123-127. https://doi.org/10.1038/ng.513
Romo-García, M.F., Bastian, Y., Zapata-Zúñiga, M., Macías-Segura, N., Castillo-Ortiz, J.D., Lara- Ramírez, E.E., Fernández-Ruiz, J., Berlanga. Taylor, A., González-Amaro, R., Ramos-Remus, C., Enciso-Moreno, J., & Castañeda-Delgado, J.E. (2019). Identification of putative miRNA biomarkers in early rheumatoid arthritis by genome-wide microarray profiling: A pilot study. Gene, 720, 144081. https://doi.org/10.1016/j.gene.2019.144081
Rothwell, S., Cooper, R.G., Lundberg, I. E., Miller, F.W., Gregersen, P. K., Bowes, J., Vencosvsky, J., Danko, C., Lymaye, V., Selva-O'Callaghan, A., Hanna, M., Machado, P., Pachman, L., Reed, A., Rider, L., Cobb, J., Platt, H., Molberg, O., Benveniste, O., Mathiessen, P., … Lamb, J. (Myositis Genetic Consortium). (2016). Dense genotyping of immune-related loci in idiopathic inf lammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups. Annals of the Rheumatic Diseases, 75(8), 1558-66. https://doi.org/10.1136/annrheumdis-2015-208119
Sánchez, E., Webb, R. D., Rasmussen, A., Kelly, J. A., Riba, L., Kaufman, K. M., García-de la Torre, I., Moctezuma, J., Maradiaga-Ceceña, M., Cardiel-Rios, M., Acevedo, E., Cucho- Venegas, M., García, M., Gamron, S., Pons-Estel, B., Vasconcelos, C., Martin, J., Tusié-Luna, T., Harley, J., Richardson, B., … Alarcón-Riquelme, M. E. (2010). Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemics lupus erythematosus. Arthritis & Rheumatology, 62(12), 3722-3729. https://doi.org/10.1002/art.27753
Selmi, C., Leung, P. S. C., Sherr, D. S., Diaz, M., Nyland, J. F., Monestier, M., Rose, N., & Gershwin, M. E. (2012a). Mechanism of environmental influence on human autoimmunity: A national institute of environmental health sciences expert panel workshop. Journal of Autoimmunity, 39, 282-284. https://doi.org/10.1016/j.jaut.2012.05.007
Selmi, C., Lu, Q., & Humble, M. C. (2012b). Heritability versus the role of the environment autoimmunity. Journal of Autoimmunity, 39, 249-252. https://doi.org/10.1016/j.jaut.2012.07.011
Shao, M., Xu, S., Yang, H., Xu, W., Deng, J., Chen, Y., Gao, X., Guan, S., Xu, S., Shuai, Z., & Pan, F. (2020). Association between IL-17A and IL- 17F gene polymorphism and susceptibility in inflammatory arthritis: A meta-analysis. Clinical Immunology 213, 108374. https://doi.org/10.1016/j.clim.2020.108374
Sisó-Almirall, A., Kostov, B., Martínez-Carbonell, E., Brito-Zerón, P., Blanch Ramirez, P., Acar- Denizli, N., Delicado, P., González-Martínez, S., Velasco Muñoz, C., Benavent Áreu, J., & Ramos-Casals, M. (2020). The prevalence of 78 autoimmune diseases in Catalonia (MASCAT- PADRIS Big Data Project). Autoimmunity Reviews, 19(2), 102448. https://doi.org/10.1016/j.autrev.2019.102448
Stahl, E. A, Raychaudhuri, S., Remmers, E. F., Xie, G., Eyre, S., Thomson B. P., Li, Y., Kurreeman, F., Zhernakova, A., Hinks, A., Guiducci, C., Chen, R., Alfredsson, L., Amos, C., Ardlie, K., Barton, A., BIRAC Consortium., Bowes, J., Burtt, N., Brouwer, E., … Plenge, R. M. (2010). Genome wide association study meta-analysis identified seven new rheumatoid arthritis risk loci. Nature Genetics, 42, 508-514. https://doi.org/10.1038/ng.582
Stanford, S. M., & Bottini, N. (2014). PTPN22: the archetypal non-HLA autoimmunity gene. Nature Review Rheumatology, 10, 602-611. https://doi.org/10.1038/nrrheum.2014.109
Teruel, M., & Alarcón-Riquelme, M. E. (2016a). The genetic basis of systemic lupus erythematosus: What are the risk factors and what have we learned. Journal of Autoimmunity, 74, 161-175. https://doi.org/10.1016/j.jaut.2016.08.001
Teruel, M., & Alarcón-Riquelme, M. E. (2016b). Genetics of systemic lupus erythematosus and Sjögren's syndrome: an update. Current Opinion Rheumatology, 28(5), 506-514. https://doi.org/10.1097/BOR.0000000000000310
van Drongelen, V., & Holoshitz. J. (2017). Human leukocyte antigen disease associations in rheumatoid arthritis. Rheumatic Diseases Clinics of North American, 43(3), 363-376. https://doi.org/10.1016/j.rdc.2017.04.003
van der Helm-van Mil, A., Verpoort, K., Le Cessie, S., Huizinga, T., De Vries, R., & Toes, R. (2007). The HLA-DRB1 shared epitope alleles differ in the interaction with smoking and predisposition to antibodies to cyclic citrullinated peptide. Arthritis & Rheumatology, 56, 425-432. https://doi.org/10.1002/art.22373
Wang, S., Wen, F., Wiley, G., Kinter, M., & Gaffney, P. (2013). An enhancer element harboring variant associated with systemic lupus erythematosus engages the TNFAIP3 promote to influence A20 expression. PLoS Genetics, 9, e1003750. https://doi.org/10.1371/journal.pgen.1003750
Xu, H., & Yin, J. (2019). HLA risk alleles and gut microbiome in ankylosing spondylitis and rheumatoid arthritis. Best Practice & Research Clinical Rheumatology, 33(6),101499. https://doi.org/10.1016/j.berh.2020.101499
Xue, K., Niu, W., & Cui, Y. (2018). Association of HLA‑DR3 and HLA‑DR15 Polymorphisms with Risk of Systemic Lupus Erythematosus. Chinese Medical Journal, 131(23), 2844-51. https://doi. org/10.4103/0366-6999.246058
Yukinori, O., Kishikawa, T., Sakaue, S., & Hirata, J. (2017). Future directions of genomics research in rheumatic diseases. Rheumatic Diseases Clinics of North American, 43(3), 481-487. https://doi.org/10.1016/j.rdc.2017.04.009
Zeng, G., Zang, W., Qian, Y., Huang, H., Wu, D., He, Z., Ye, D., Mao, Y., & Wen, C. (2020). Association of telomere length with risk of rheumatoid arthritis: a meta-analysis and Mendelian randomization. Rheumatology, 59(5), 940 -947. https://doi.org/10.1093/rheumatology/kez524
Zheng, J., Yin, J., Huang, R., Peterson, F., & Yu, X. (2013). Meta-analysis reveals an association of STAT4 polymorphisms with systemic autoimmune disorders and anti dsDNA antibody. Human Immunology, 74, 986-992. https://doi.org/10.1016/j.humimm.2013.04.034
Descargas
Publicado
Cómo citar
Número
Sección
Licencia
Derechos de autor 2021 Maynor A. Herrera
Esta obra está bajo una licencia internacional Creative Commons Atribución-NoComercial-CompartirIgual 4.0.
El autor que publique en esta revista acepta las siguientes condiciones:
- El autor otorga a la Dirección General de Investigación el derecho de editar, reproducir, publicar y difundir el manuscrito en forma impresa o electrónica en la revista Ciencia, Tecnología y Salud.
- La Direción General de Investigación otorgará a la obra una licencia Creative Commons Atribución-NoComercial-CompartirIgual 4.0 Internacional