JOSE EDUARDO KRIEGER

(Fonte: Lattes)
Índice h a partir de 2011
36
Projetos de Pesquisa
Unidades Organizacionais
Departamento de Cardio-Pneumologia, Faculdade de Medicina - Docente
Instituto do Coração, Hospital das Clínicas, Faculdade de Medicina
LIM/13 - Laboratório de Genética e Cardiologia Molecular, Hospital das Clínicas, Faculdade de Medicina - Líder

Resultados de Busca

Agora exibindo 1 - 3 de 3
  • article 14 Citação(ões) na Scopus
    Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure
    (2021) WANG, Heming; NOORDAM, Raymond; CADE, Brian E.; SCHWANDER, Karen; WINKLER, Thomas W.; LEE, Jiwon; SUNG, Yun Ju; BENTLEY, Amy R.; MANNING, Alisa K.; ASCHARD, Hugues; KILPELAINEN, Tuomas O.; ILKOV, Marjan; BROWN, Michael R.; HORIMOTO, Andrea R.; RICHARD, Melissa; BARTZ, Traci M.; VOJINOVIC, Dina; LIM, Elise; NIERENBERG, Jovia L.; LIU, Yongmei; CHITRALA, Kumaraswamynaidu; RANKINEN, Tuomo; MUSANI, Solomon K.; FRANCESCHINI, Nora; RAURAMAA, Rainer; ALVER, Maris; ZEE, Phyllis C.; HARRIS, Sarah E.; MOST, Peter J. van Der; NOLTE, Ilja M.; MUNROE, Patricia B.; PALMER, Nicholette D.; KUHNEL, Brigitte; WEISS, Stefan; WEN, Wanqing; HALL, Kelly A.; LYYTIKAINEN, Leo-Pekka; CONNELL, Jeff O.; EIRIKSDOTTIR, Gudny; LAUNER, Lenore J.; VRIES, Paul S. de; ARKING, Dan E.; CHEN, Han; BOERWINKLE, Eric; KRIEGER, Jose E.; SCHREINER, Pamela J.; SIDNEY, Stephen; SHIKANY, James M.; RICE, Kenneth; CHEN, Yii-Der Ida; GHARIB, Sina A.; BIS, Joshua C.; I, Annemarie Luik; IKRAM, M. Arfan; UITTERLINDEN, Andre G.; AMIN, Najaf; XU, Hanfei; LEVY, Daniel; HE, Jiang; LOHMAN, Kurt K.; ZONDERMAN, Alan B.; RICE, Treva K.; SIMS, Mario; WILSON, Gregory; SOFER, Tamar; RICH, Stephen S.; PALMAS, Walter; YAO, Jie; GUO, Xiuqing; I, Jerome Rotter; BIERMASZ, Nienke R.; MOOK-KANAMORI, Dennis O.; MARTIN, Lisa W.; BARAC, Ana; WALLACE, Robert B.; GOTTLIEB, Daniel J.; KOMULAINEN, Pirjo; HEIKKINEN, Sami; MAGI, Reedik; MILANI, Lili; METSPALU, Andres; STARR, John M.; MILANESCHI, Yuri; WAKEN, R. J.; GAO, Chuan; WALDENBERGER, Melanie; PETERS, Annette; STRAUCH, Konstantin; MEITINGER, Thomas; ROENNEBERG, Till; VOLKER, Uwe; DORR, Marcus; SHU, Xiao-Ou; MUKHERJEE, Sutapa; HILLMAN, David R.; KAHONEN, Mika; WAGENKNECHT, Lynne E.; GIEGER, Christian; GRABE, Hans J.; ZHENG, Wei; PALMER, Lyle J.; LEHTIMAKI, Terho; GUDNASON, Vilmundur; MORRISON, Alanna C.; PEREIRA, Alexandre C.; FORNAGE, Myriam; PSATY, Bruce M.; DUIJN, Cornelia M. van; LIU, Ching-Ti; KELLY, Tanika N.; EVANS, Michele K.; BOUCHARD, Claude; FOX, Ervin R.; KOOPERBERG, Charles; ZHU, Xiaofeng; LAKKA, Timo A.; ESKO, Tonu; NORTH, Kari E.; DEARY, Ian J.; SNIEDER, Harold; PENNINX, Brenda W. J. H.; GAUDERMAN, W. James; RAO, Dabeeru C.; REDLINE, Susan; HEEMST, Diana van
    Long and short sleep duration are associated with elevated blood pressure (BP), possibly through effects on molecular pathways that influence neuroendocrine and vascular systems. To gain new insights into the genetic basis of sleep-related BP variation, we performed genome-wide gene by short or long sleep duration interaction analyses on four BP traits (systolic BP, diastolic BP, mean arterial pressure, and pulse pressure) across five ancestry groups in two stages using 2 degree of freedom (df) joint test followed by 1df test of interaction effects. Primary multi-ancestry analysis in 62,969 individuals in stage 1 identified three novel gene by sleep interactions that were replicated in an additional 59,296 individuals in stage 2 (stage 1 + 2 P-joint < 5 x 10(-8)), including rs7955964 (FIGNL2/ANKRD33) that increases BP among long sleepers, and rs73493041 (SNORA26/C9orf170) and rs10406644 (KCTD15/LSM14A) that increase BP among short sleepers (P-int < 5 x 10(-8)). Secondary ancestry-specific analysis identified another novel gene by long sleep interaction at rs111887471 (TRPC3/KIAA1109) in individuals of African ancestry (P-int = 2 x 10(-6)). Combined stage 1 and 2 analyses additionally identified significant gene by long sleep interactions at 10 loci including MKLN1 and RGL3/ELAVL3 previously associated with BP, and significant gene by short sleep interactions at 10 loci including C2orf43 previously associated with BP (P-int < 10(-3)). 2df test also identified novel loci for BP after modeling sleep that has known functions in sleep-wake regulation, nervous and cardiometabolic systems. This study indicates that sleep and primary mechanisms regulating BP may interact to elevate BP level, suggesting novel insights into sleep-related BP regulation.
  • article 13 Citação(ões) na Scopus
    Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
    (2021) FUENTES, Lisa de las; SUNG, Yun Ju; NOORDAM, Raymond; WINKLER, Thomas; FEITOSA, Mary F.; SCHWANDER, Karen; BENTLEY, Amy R.; BROWN, Michael R.; GUO, Xiuqing; MANNING, Alisa; CHASMAN, Daniel I.; ASCHARD, Hugues; BARTZ, Traci M.; BIELAK, Lawrence F.; CAMPBELL, Archie; CHENG, Ching-Yu; DORAJOO, Rajkumar; HARTWIG, Fernando P.; HORIMOTO, A. R. V. R.; LI, Changwei; LI-GAO, Ruifang; LIU, Yongmei; MARTEN, Jonathan; MUSANI, Solomon K.; NTALLA, Ioanna; RANKINEN, Tuomo; RICHARD, Melissa; SIM, Xueling; SMITH, Albert V.; TAJUDDIN, Salman M.; TAYO, Bamidele O.; VOJINOVIC, Dina; WARREN, Helen R.; XUAN, Deng; ALVER, Maris; BOISSEL, Mathilde; CHAI, Jin-Fang; CHEN, Xu; CHRISTENSEN, Kaare; DIVERS, Jasmin; EVANGELOU, Evangelos; GAO, Chuan; GIROTTO, Giorgia; HARRIS, Sarah E.; HE, Meian; HSU, Fang-Chi; KUEHNEL, Brigitte; LAGUZZI, Federica; LI, Xiaoyin; LYYTIKAINEN, Leo-Pekka; NOLTE, Ilja M.; POVEDA, Alaitz; RAURAMAA, Rainer; RIAZ, Muhammad; RUEEDI, Rico; SHU, Xiao-ou; SNIEDER, Harold; SOFER, Tamar; TAKEUCHI, Fumihiko; VERWEIJ, Niek; WARE, Erin B.; WEISS, Stefan; YANEK, Lisa R.; AMIN, Najaf; ARKING, Dan E.; ARNETT, Donna K.; BERGMANN, Sven; BOERWINKLE, Eric; BRODY, Jennifer A.; BROECKEL, Ulrich; BRUMAT, Marco; BURKE, Gregory; CABRERA, Claudia P.; CANOUIL, Mickael; CHEE, Miao Li; CHEN, Yii-Der Ida; COCCA, Massimiliano; CONNELL, John; SILVA, H. Janaka de; VRIES, Paul S. de; EIRIKSDOTTIR, Gudny; FAUL, Jessica D.; FISHER, Virginia; FORRESTER, Terrence; FOX, Ervin F.; FRIEDLANDER, Yechiel; GAO, He; GIGANTE, Bruna; GIULIANINI, Franco; GU, Chi Charles; GU, Dongfeng; HARRIS, Tamara B.; HE, Jiang; HEIKKINEN, Sami; HENG, Chew-Kiat; HUNT, Steven; IKRAM, M. Arfan; IRVIN, Marguerite R.; KAHONEN, Mika; KAVOUSI, Maryam; KHOR, Chiea Chuen; KILPELAINEN, Tuomas O.; KOH, Woon-Puay; KOMULAINEN, Pirjo; KRAJA, Aldi T.; KRIEGER, J. E.; LANGEFELD, Carl D.; LI, Yize; LIANG, Jingjing; LIEWALD, David C. M.; LIU, Ching-Ti; LIU, Jianjun; LOHMAN, Kurt K.; MAGI, Reedik; MCKENZIE, Colin A.; MEITINGER, Thomas; METSPALU, Andres; MILANESCHI, Yuri; MILANI, Lili; MOOK-KANAMORI, Dennis O.; NALLS, Mike A.; NELSON, Christopher P.; NORRIS, Jill M.; O'CONNELL, Jeff; OGUNNIYI, Adesola; PADMANABHAN, Sandosh; PALMER, Nicholette D.; PEDERSEN, Nancy L.; PERLS, Thomas; PETERS, Annette; PETERSMANN, Astrid; PEYSER, Patricia A.; POLASEK, Ozren; PORTEOUS, David J.; RAFFEL, Leslie J.; RICE, Treva K.; ROTTER, Jerome I.; RUDAN, Igor; RUEDA-OCHOA, Oscar-Leonel; SABANAYAGAM, Charumathi; SALAKO, Babatunde L.; SCHREINER, Pamela J.; SHIKANY, James M.; SIDNEY, Stephen S.; SIMS, Mario; SITLANI, Colleen M.; SMITH, Jennifer A.; STARR, John M.; STRAUCH, Konstantin; SWERTZ, Morris A.; TEUMER, Alexander; THAM, Yih Chung; UITTERLINDEN, Andre G.; VAIDYA, Dhananjay; ENDE, M. Yldau van der; WALDENBERGER, Melanie; WANG, Lihua; WANG, Ya-Xing; WEI, Wen-Bin; WEIR, David R.; WEN, Wanqing; YAO, Jie; YU, Bing; YU, Caizheng; YUAN, Jian-Min; ZHAO, Wei; ZONDERMAN, Alan B.; BECKER, Diane M.; BOWDEN, Donald W.; DEARY, Ian J.; DOERR, Marcus; ESKO, Tonu; FREEDMAN, Barry I.; FROGUEL, Philippe; GASPARINI, Paolo; GIEGER, Christian; JONAS, Jost Bruno; KAMMERER, Candace M.; KATO, Norihiro; LAKKA, Timo A.; LEANDER, Karin; LEHTIMAKI, Terho; MAGNUSSON, Patrik K. E.; MARQUES-VIDAL, Pedro; PENNINX, Brenda W. J. H.; SAMANI, Nilesh J.; HARST, Pim van der; WAGENKNECHT, Lynne E.; WU, Tangchun; ZHENG, Wei; ZHU, Xiaofeng; BOUCHARD, Claude; COOPER, Richard S.; CORREA, Adolfo; EVANS, Michele K.; GUDNASON, Vilmundur; HAYWARD, Caroline; HORTA, Bernardo L.; KELLY, Tanika N.; KRITCHEVSKY, Stephen B.; LEVY, Daniel; PALMAS, Walter R.; PEREIRA, A. C.; PROVINCE, Michael M.; PSATY, Bruce M.; RIDKER, Paul M.; ROTIMI, Charles N.; TAI, E. Shyong; DAM, Rob M. van; DUIJN, Cornelia M. van; WONG, Tien Yin; RICE, Kenneth; GAUDERMAN, W. James; MORRISON, Alanna C.; NORTH, Kari E.; KARDIA, Sharon L. R.; CAULFIELD, Mark J.; ELLIOTT, Paul; MUNROE, Patricia B.; FRANKS, Paul W.; RAO, Dabeeru C.; FORNAGE, Myriam
    Educational attainment is widely used as a surrogate for socioeconomic status (SES). Low SES is a risk factor for hypertension and high blood pressure (BP). To identify novel BP loci, we performed multi-ancestry meta-analyses accounting for gene-educational attainment interactions using two variables, ""Some College"" (yes/no) and ""Graduated College"" (yes/no). Interactions were evaluated using both a 1 degree of freedom (DF) interaction term and a 2DF joint test of genetic and interaction effects. Analyses were performed for systolic BP, diastolic BP, mean arterial pressure, and pulse pressure. We pursued genome-wide interrogation in Stage 1 studies (N = 117 438) and follow-up on promising variants in Stage 2 studies (N = 293 787) in five ancestry groups. Through combined meta-analyses of Stages 1 and 2, we identified 84 known and 18 novel BP loci at genome-wide significance level (P < 5 x 10(-8)). Two novel loci were identified based on the 1DF test of interaction with educational attainment, while the remaining 16 loci were identified through the 2DF joint test of genetic and interaction effects. Ten novel loci were identified in individuals of African ancestry. Several novel loci show strong biological plausibility since they involve physiologic systems implicated in BP regulation. They include genes involved in the central nervous system-adrenal signaling axis (ZDHHC17, CADPS, PIK3C2G), vascular structure and function (GNB3, CDON), and renal function (HAS2 and HAS2-AS1, SLIT3). Collectively, these findings suggest a role of educational attainment or SES in further dissection of the genetic architecture of BP.
  • article 6 Citação(ões) na Scopus
    Evening preference correlates with regional brain volumes in the anterior occipital lobe
    (2021) EVANS, SL.; LEOCADIO-MIGUEL, M. A.; TAPOROSKI, T. P.; GOMEZ, L. M.; HORIMOTO, A. R. V. R.; ALKAN, E.; BEIJAMINI, F.; PEDRAZZOLI, M.; KNUTSON, K. L.; KRIEGER, J. E.; VALLADA, H. P.; STERR, A.; PEREIRA, A. C.; NEGRAO, A. B.; SCHANTZ, M. von
    Chronotype or diurnal preference is a questionnaire-based measure influenced both by circadian period and by the sleep homeostat. In order to further characterize the biological determinants of these measures, we used a hypothesis-free approach to investigate the association between the score of the morningness-eveningness questionnaire (MEQ) and the Munich chronotype questionnaire (MCTQ), as continuous variables, and volumetric measures of brain regions acquired by magnetic resonance imaging (MRI). Data were collected from the Baependi Heart Study cohort, based in a rural town in South-Eastern Brazil. MEQ and anatomical 1.5-T MRI scan data were available from 410 individuals, and MCTQ scores were available from a subset of 198 of them. The average MEQ (62.2 +/- 10.6) and MCTQ (average MSFsc 201 +/- 85 min) scores were suggestive of a previously reported strong general tendency toward morningness in this community. Setting the significance threshold at P > .002 to account for multiple comparisons, we observed a significant association between lower MEQ score (eveningness) and greater volume of the left anterior occipital sulcus (beta = -0.163, p = .001) of the occipital lobe. No significant associations were observed for MCTQ. This may reflect the smaller dataset for MCTQ, and/or the fact that MEQ, which asks questions about preferred timings, is more trait-like than the MCTQ, which asks questions about actual timings. The association between MEQ and a brain region dedicated to visual information processing is suggestive of the increasingly recognized fluidity in the interaction between visual and nonvisual photoreception and the circadian system, and the possibility that chronotype includes an element of masking.