首页 > 最新文献

1500 – Genetics最新文献

英文 中文
1507 The relationship between DNA methylation patterns and disease activity in a longitudinal multi-ancestral cohort of lupus patients 1507在狼疮患者的纵向多祖先队列中DNA甲基化模式与疾病活动性的关系
Pub Date : 2021-11-01 DOI: 10.1136/lupus-2021-lupus21century.90
P. Coit, L. Ortiz-Fernández, E. Lewis, W. Joseph McCune, K. Maksimowicz-McKinnon, A. Sawalha
{"title":"1507 The relationship between DNA methylation patterns and disease activity in a longitudinal multi-ancestral cohort of lupus patients","authors":"P. Coit, L. Ortiz-Fernández, E. Lewis, W. Joseph McCune, K. Maksimowicz-McKinnon, A. Sawalha","doi":"10.1136/lupus-2021-lupus21century.90","DOIUrl":"https://doi.org/10.1136/lupus-2021-lupus21century.90","url":null,"abstract":"","PeriodicalId":253913,"journal":{"name":"1500 – Genetics","volume":"38 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134431380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
1505 Genetics: flipons and the role of the left-handed Z-RNA conformation in interferonopathies 1505遗传学:翻转和左旋Z-RNA构象在干扰素病变中的作用
Pub Date : 2021-11-01 DOI: 10.1136/lupus-2021-lupus21century.88
A. Herbert
{"title":"1505 Genetics: flipons and the role of the left-handed Z-RNA conformation in interferonopathies","authors":"A. Herbert","doi":"10.1136/lupus-2021-lupus21century.88","DOIUrl":"https://doi.org/10.1136/lupus-2021-lupus21century.88","url":null,"abstract":"","PeriodicalId":253913,"journal":{"name":"1500 – Genetics","volume":"7 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131318315","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
1502 Genetic predisposition to lupus across ancestries has >300 separable genetic contributions: what we know today 1502 .狼疮的遗传易感性有超过300个可分离的遗传贡献:我们今天所知道的
Pub Date : 2021-11-01 DOI: 10.1136/lupus-2021-lupus21century.85
Viktoryia Laurynenka, L. Kottyan, M. Weirauch, K. Kaufman, J. Harley
{"title":"1502 Genetic predisposition to lupus across ancestries has >300 separable genetic contributions: what we know today","authors":"Viktoryia Laurynenka, L. Kottyan, M. Weirauch, K. Kaufman, J. Harley","doi":"10.1136/lupus-2021-lupus21century.85","DOIUrl":"https://doi.org/10.1136/lupus-2021-lupus21century.85","url":null,"abstract":"","PeriodicalId":253913,"journal":{"name":"1500 – Genetics","volume":"26 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115123319","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
1504 The influence of dietary resistant starch content on the gut microbiota of patients with systemic lupus erythematosus and antiphospholipid syndrome 1504 .膳食抗性淀粉含量对系统性红斑狼疮合并抗磷脂综合征患者肠道菌群的影响
Pub Date : 2021-11-01 DOI: 10.1136/lupus-2021-lupus21century.87
I. Kulyk, M. S. Pereira, S. Redanz, W. Ruff, T. Greiling, C. Dehner, O. Pagovich, Daniel Zegarra Ruiz, Cassyanne L. Aguiar, D. Erkan, M. Kriegel
{"title":"1504 The influence of dietary resistant starch content on the gut microbiota of patients with systemic lupus erythematosus and antiphospholipid syndrome","authors":"I. Kulyk, M. S. Pereira, S. Redanz, W. Ruff, T. Greiling, C. Dehner, O. Pagovich, Daniel Zegarra Ruiz, Cassyanne L. Aguiar, D. Erkan, M. Kriegel","doi":"10.1136/lupus-2021-lupus21century.87","DOIUrl":"https://doi.org/10.1136/lupus-2021-lupus21century.87","url":null,"abstract":"","PeriodicalId":253913,"journal":{"name":"1500 – Genetics","volume":"199 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124380608","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
1508 Single-cell epigenetic profiling highlights genetic impact on chromatin accessibility in SLE 1508单细胞表观遗传分析强调SLE患者染色质可及性的遗传影响
Pub Date : 2021-11-01 DOI: 10.1136/lupus-2021-lupus21century.91
Sai Ma, Richard C. Pelikan, Yao Fu, J. Kelly, David Murphy, G. Wiley, Vinay K. Kartha, C. Lareau, Jason D. Buenrostro, P. Gaffney
{"title":"1508 Single-cell epigenetic profiling highlights genetic impact on chromatin accessibility in SLE","authors":"Sai Ma, Richard C. Pelikan, Yao Fu, J. Kelly, David Murphy, G. Wiley, Vinay K. Kartha, C. Lareau, Jason D. Buenrostro, P. Gaffney","doi":"10.1136/lupus-2021-lupus21century.91","DOIUrl":"https://doi.org/10.1136/lupus-2021-lupus21century.91","url":null,"abstract":"","PeriodicalId":253913,"journal":{"name":"1500 – Genetics","volume":"46 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117141103","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
1509 Differences in chromatin architecture pre- and post-induction therapy in pediatric lupus patients 儿童狼疮患者诱导治疗前后染色质结构的差异
Pub Date : 2021-11-01 DOI: 10.1136/lupus-2021-lupus21century.92
J. Hui-Yuen, K. Jiang, S. Malkiel, B. Diamond, J. Jarvis
{"title":"1509 Differences in chromatin architecture pre- and post-induction therapy in pediatric lupus patients","authors":"J. Hui-Yuen, K. Jiang, S. Malkiel, B. Diamond, J. Jarvis","doi":"10.1136/lupus-2021-lupus21century.92","DOIUrl":"https://doi.org/10.1136/lupus-2021-lupus21century.92","url":null,"abstract":"","PeriodicalId":253913,"journal":{"name":"1500 – Genetics","volume":"35 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115496956","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
1501 Genetics of age at systemic lupus erythematosus diagnosis 1501年龄遗传学对系统性红斑狼疮诊断的影响
Pub Date : 2021-11-01 DOI: 10.1136/lupus-2021-lupus21century.84
R. Carlomagno, FangMing Liao, Jing-chao Cao, D. Dominguez, D. Gladman, Mariko Ishimori, C. Jefferies, D. Kamen, S. Kamphuis, M. Klein‐gitelman, A. Knight, Chia-Chi J Lee, D. Levy, K. Onel, A. D. Paterson, C. Peschken, J. Pope, Z. Touma, M. Urowitz, D. Wallace, Declan Webber, J. Wither, E. Silverman, L. Hiraki
{"title":"1501 Genetics of age at systemic lupus erythematosus diagnosis","authors":"R. Carlomagno, FangMing Liao, Jing-chao Cao, D. Dominguez, D. Gladman, Mariko Ishimori, C. Jefferies, D. Kamen, S. Kamphuis, M. Klein‐gitelman, A. Knight, Chia-Chi J Lee, D. Levy, K. Onel, A. D. Paterson, C. Peschken, J. Pope, Z. Touma, M. Urowitz, D. Wallace, Declan Webber, J. Wither, E. Silverman, L. Hiraki","doi":"10.1136/lupus-2021-lupus21century.84","DOIUrl":"https://doi.org/10.1136/lupus-2021-lupus21century.84","url":null,"abstract":"","PeriodicalId":253913,"journal":{"name":"1500 – Genetics","volume":"117 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123495486","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
1510 Predicting risk of severe lupus nephritis in African Americans: the APOL1 story 1510预测非裔美国人严重狼疮肾炎的风险:APOL1的故事
Pub Date : 2021-11-01 DOI: 10.1136/lupus-2021-lupus21century.93
B. Freedman
BackgroundCompared to European, Asian and Native Americans, African Americans have a 3-fold higher risk of developing end-stage kidney disease (ESKD) and are more likely to develop severe lupus nephritis (LN).MethodsStrong genetic association is observed between the apolipoprotein L1 gene (APOL1) and a spectrum of non-diabetic chronic kidney diseases (CKD) in African Americans, including LN, focal segmental glomerulosclerosis, solidified glomerulosclerosis (hypertension-attributed nephropathy), HIV-associated nephropathy, sickle cell nephropathy, and premature failure of transplanted kidneys from APOL1 high-risk donors. APOL1 risk variants arose in sub-Saharan Africa and are present only in those who possess recent African ancestry. These variants account for much of the excess risk for LN and CKD in African Americans. Studies in transgenic mice prove that APOL1 risk variants cause CKD. Kidney disease is due to locally produced APOL1 protein in kidney cells, not circulating APOL1 protein in the blood.ResultsPatients with systemic lupus erythematosus who inherit two APOL1 risk variants are more likely to progress to ESKD and often display focal and diffuse proliferative or membranous glomerular lesions. Kidney disease often progresses despite cytotoxic therapy. In contrast, APOL1 is not associated with mild LN. Therefore, APOL1 risk variants are nephropathy progression factors. Not all individuals with two APOL1 risk variants develop CKD;modifying factors are required. HIV infection, SARS-CoV-2 infection, and interferon are powerful second hits that initiate nephropathy in genetically susceptible hosts.ConclusionsConventional treatments for kidney disease often fail to halt the progression of non-diabetic CKD. Novel small molecule inhibitors of APOL1 protein and APOL1 anti-sense oligonucleotides hold great promise for slowing progression of APOL1-associated nephropathy, including LN. Treatments have the potential to reduce disparities in CKD risk among individuals with African ancestry. In addition, the NIH ‘APOL1 Long-term Kidney Transplant Outcomes’ (APOLLO) Consortium is considering the role of APOL1 genotyping in deceased African American kidney donors to improve organ allocation. Discovery of the APOL1 genetic association with nephropathy in the lab has moved to the bedside and will improve patient outcomes.
与欧洲人、亚洲人和印第安人相比,非洲裔美国人患终末期肾病(ESKD)的风险高出3倍,更有可能发展为严重的狼疮性肾炎(LN)。方法观察载脂蛋白L1基因(APOL1)与非糖尿病性慢性肾病(CKD)谱之间的强烈遗传关联,包括LN、局灶节段性肾小球硬化、固化肾小球硬化(高血压肾病)、hiv相关肾病、镰状细胞肾病和APOL1高危供者移植肾脏的过早衰竭。APOL1风险变异出现在撒哈拉以南非洲,仅存在于最近拥有非洲血统的人身上。这些变异是非裔美国人患LN和CKD的主要原因。转基因小鼠的研究证明,APOL1风险变异导致CKD。肾脏疾病是由于肾细胞中局部产生的APOL1蛋白,而不是血液中循环的APOL1蛋白。结果遗传两个APOL1风险变异的系统性红斑狼疮患者更有可能发展为ESKD,并经常表现为局灶性和弥漫性增生性或膜性肾小球病变。尽管细胞毒性治疗,肾脏疾病仍常进展。相反,APOL1与轻度LN无关。因此,APOL1风险变异是肾病进展因素。并非所有具有两种APOL1风险变异的个体都会发展为CKD,需要调节因素。HIV感染、SARS-CoV-2感染和干扰素是在遗传易感宿主中引发肾病的强大二次打击。结论肾脏疾病的常规治疗往往不能阻止非糖尿病性CKD的进展。APOL1蛋白和APOL1反义寡核苷酸的新型小分子抑制剂对减缓包括LN在内的APOL1相关肾病的进展具有很大的希望。治疗有可能减少非洲血统个体之间CKD风险的差异。此外,NIH“APOL1长期肾移植结果”(APOLLO)联盟正在考虑APOL1基因分型在已故非裔美国肾供者中的作用,以改善器官分配。实验室发现的APOL1基因与肾病的关联已经转移到床边,并将改善患者的预后。
{"title":"1510 Predicting risk of severe lupus nephritis in African Americans: the APOL1 story","authors":"B. Freedman","doi":"10.1136/lupus-2021-lupus21century.93","DOIUrl":"https://doi.org/10.1136/lupus-2021-lupus21century.93","url":null,"abstract":"BackgroundCompared to European, Asian and Native Americans, African Americans have a 3-fold higher risk of developing end-stage kidney disease (ESKD) and are more likely to develop severe lupus nephritis (LN).MethodsStrong genetic association is observed between the apolipoprotein L1 gene (APOL1) and a spectrum of non-diabetic chronic kidney diseases (CKD) in African Americans, including LN, focal segmental glomerulosclerosis, solidified glomerulosclerosis (hypertension-attributed nephropathy), HIV-associated nephropathy, sickle cell nephropathy, and premature failure of transplanted kidneys from APOL1 high-risk donors. APOL1 risk variants arose in sub-Saharan Africa and are present only in those who possess recent African ancestry. These variants account for much of the excess risk for LN and CKD in African Americans. Studies in transgenic mice prove that APOL1 risk variants cause CKD. Kidney disease is due to locally produced APOL1 protein in kidney cells, not circulating APOL1 protein in the blood.ResultsPatients with systemic lupus erythematosus who inherit two APOL1 risk variants are more likely to progress to ESKD and often display focal and diffuse proliferative or membranous glomerular lesions. Kidney disease often progresses despite cytotoxic therapy. In contrast, APOL1 is not associated with mild LN. Therefore, APOL1 risk variants are nephropathy progression factors. Not all individuals with two APOL1 risk variants develop CKD;modifying factors are required. HIV infection, SARS-CoV-2 infection, and interferon are powerful second hits that initiate nephropathy in genetically susceptible hosts.ConclusionsConventional treatments for kidney disease often fail to halt the progression of non-diabetic CKD. Novel small molecule inhibitors of APOL1 protein and APOL1 anti-sense oligonucleotides hold great promise for slowing progression of APOL1-associated nephropathy, including LN. Treatments have the potential to reduce disparities in CKD risk among individuals with African ancestry. In addition, the NIH ‘APOL1 Long-term Kidney Transplant Outcomes’ (APOLLO) Consortium is considering the role of APOL1 genotyping in deceased African American kidney donors to improve organ allocation. Discovery of the APOL1 genetic association with nephropathy in the lab has moved to the bedside and will improve patient outcomes.","PeriodicalId":253913,"journal":{"name":"1500 – Genetics","volume":"20 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134397375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
1503 High-throughput identification of regulatory functional Snps associated with systemic lupus erythematosus 1503与系统性红斑狼疮相关的调控功能snp的高通量鉴定
Pub Date : 2021-11-01 DOI: 10.1136/lupus-2021-lupus21century.86
Qiang Wang, Marta Martinez Bonet, M. Weirauch, P. Nigrovic
{"title":"1503 High-throughput identification of regulatory functional Snps associated with systemic lupus erythematosus","authors":"Qiang Wang, Marta Martinez Bonet, M. Weirauch, P. Nigrovic","doi":"10.1136/lupus-2021-lupus21century.86","DOIUrl":"https://doi.org/10.1136/lupus-2021-lupus21century.86","url":null,"abstract":"","PeriodicalId":253913,"journal":{"name":"1500 – Genetics","volume":"17 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125374052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
1500 – Genetics
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1