Page last updated: 2024-10-24

caffeine and Genetic Predisposition

caffeine has been researched along with Genetic Predisposition in 80 studies

Research Excerpts

ExcerptRelevanceReference
"Our aim was to observe the induction of anxiety symptoms and panic attacks by a caffeine challenge test in panic disorder (PD) patients (DSM-IV) and their healthy first-degree relatives."9.13A caffeine challenge test in panic disorder patients, their healthy first-degree relatives, and healthy controls. ( de-Melo-Neto, VL; Freire, RC; King, AL; Lopes, FL; Mezzasalma, MA; Nardi, AE; Nascimento, I; Rassi, A; Soares-Filho, GL; Valença, AM; Veras, AB; Zin, WA, 2008)
"This review summarizes and highlights recent advances in current knowledge of the relationship between coffee and caffeine consumption and risk of coronary heart disease."8.84Coffee, caffeine, and coronary heart disease. ( Cornelis, MC; El-Sohemy, A, 2007)
"Some case-control studies have demonstrated that caffeine intake and high CYP1A2 activity increase risks of recurrent pregnancy loss (RPL) but the multifactorial effect is obscure."7.73Caffeine intake, CYP1A2 polymorphism and the risk of recurrent pregnancy loss. ( Kato, EH; Kishi, R; Minakami, H; Morikawa, M; Saijo, Y; Sata, F; Suzuki, K; Yamada, H, 2005)
"Our aim was to observe the induction of anxiety symptoms and panic attacks by a caffeine challenge test in panic disorder (PD) patients (DSM-IV) and their healthy first-degree relatives."5.13A caffeine challenge test in panic disorder patients, their healthy first-degree relatives, and healthy controls. ( de-Melo-Neto, VL; Freire, RC; King, AL; Lopes, FL; Mezzasalma, MA; Nardi, AE; Nascimento, I; Rassi, A; Soares-Filho, GL; Valença, AM; Veras, AB; Zin, WA, 2008)
"This review summarizes and highlights recent advances in current knowledge of the relationship between coffee and caffeine consumption and risk of coronary heart disease."4.84Coffee, caffeine, and coronary heart disease. ( Cornelis, MC; El-Sohemy, A, 2007)
"NAT2 acetylation status was determined by both single nucleotide polymorphisms (SNPs) and caffeine metabolic ratio (CMR), in a population-based study of 494 bladder cancer patients and 507 control subjects in Shanghai, China."3.83Differential association for N-acetyltransferase 2 genotype and phenotype with bladder cancer risk in Chinese population. ( Chan, KK; Chattopadhyay, K; Gao, YT; Nelson, HH; Quan, L; Wang, R; Xiang, YB; Yuan, JM; Zhang, W, 2016)
"Animal models have suggested that oral or topical administration of caffeine could inhibit ultraviolet-induced carcinogenesis via the ataxia telangiectasia and rad3 (ATR)-related apoptosis."3.83A genome-wide analysis of gene-caffeine consumption interaction on basal cell carcinoma. ( Cornelis, MC; De Vivo, I; Giovannucci, E; Han, J; Li, X; Liang, L; Song, F; Tang, JY, 2016)
"The aim of the present study was to evaluate the relative contribution of CYP1A2 isoforms (-3860 G/A, -2467T/delT and -163C/A) in control subjects and breast cancer patients to the metabolism of caffeine in human liver."3.81Breast Cancer Association with CYP1A2 Activity and Gene Polymorphisms--a Preliminary Case-control Study in Tunisia. ( Arij, M; Imene, A; Maurice, AJ; Saad, S; Sofia, P, 2015)
"Coffee and tea contain numerous antimutagenic and antioxidant components and high levels of caffeine that may protect against colorectal cancer (CRC)."3.80Coffee and tea consumption, genotype-based CYP1A2 and NAT2 activity and colorectal cancer risk-results from the EPIC cohort study. ( Aleksandrova, K; Argüelles, M; Barricarte, A; Bech, BH; Boeing, H; Boutron-Ruault, MC; Braaten, T; Bueno-de-Mesquita, HB; Campa, D; Cauchi, S; Chirlaque, MD; Dik, VK; Dorronsoro, M; Engeset, D; Fagherazzi, G; Freisling, H; Froguel, P; Grioni, S; Gunter, MJ; Jenab, M; Jirström, K; Khaw, KT; Kühn, T; Licaj, I; Ljuslinder, I; Murphy, N; Nilsson, LM; Oikonomou, E; Olsen, A; Overvad, K; Palli, D; Panico, S; Peeters, PH; Peppa, E; Racine, A; Riboli, E; Romaguera-Bosch, D; Sánchez, MJ; Siersema, PD; Tjønneland, A; Travis, RC; Trichopoulou, A; Tumino, R; Uiterwaal, CS; Van Duijnhoven, FJ; Van Gils, CH; Van Oijen, MG; Vineis, P; Wallström, P; Wareham, N; Weiderpass, E; Yengo, L; Zamora-Ros, R, 2014)
"A web-based sample (n=43,799 including both members of 609 twin and 303 sibling pairs) completed assessments of number of lifetime gambling episodes, DSM-IV criteria for PG, alcohol, nicotine and caffeine intake, and nicotine dependence (ND) and DSM-III-R criteria for lifetime major depression (MD)."3.78Gambling, disordered gambling and their association with major depression and substance use: a web-based cohort and twin-sibling study. ( Blanco, C; Kendler, KS; Myers, J, 2012)
"Some case-control studies have demonstrated that caffeine intake and high CYP1A2 activity increase risks of recurrent pregnancy loss (RPL) but the multifactorial effect is obscure."3.73Caffeine intake, CYP1A2 polymorphism and the risk of recurrent pregnancy loss. ( Kato, EH; Kishi, R; Minakami, H; Morikawa, M; Saijo, Y; Sata, F; Suzuki, K; Yamada, H, 2005)
"The NAT acetylator status was determined by measuring urinary caffeine metabolites in 134 nonpregnant women with a history of preeclampsia and in 109 control women with uncomplicated pregnancy."3.73N-acetyl-transferase phenotype and risk for preeclampsia. ( Peters, WH; Raijmakers, MT; Roes, EM; Steegers, EA; Steegers-Theunissen, RP; te Morsche, RH; Zusterzeel, PL, 2005)
"The expression of common fragile sites induced by aphidicolin and caffeine was evaluated on prometaphase obtained from the peripheral blood lymphocytes of 35 women with breast cancer, their 35 clinically healthy female family members, and 20 sex- and age-matched normal controls."3.70Common fragile site expression and genetic predisposition to breast cancer. ( Ceçener, G; Duman, H; Egeli, U; Kizil, A; Taşdelen, I; Tunca, B, 1998)
"DNA-based diagnosis for malignant hyperthermia (MH) is an attractive proposition, because it could replace the invasive and morbid caffeine-halothane/in vitro contracture tests of skeletal muscle biopsy tissue."2.50DNA testing for malignant hyperthermia: the reality and the dream. ( Stowell, KM, 2014)
"The problem of malignant hyperthermia may become worse in the near future due to changes in the population brought about by immigration."2.44[Anesthesia in malignant hyperthermia]. ( Ortiz Gómez, JR, 2008)
"Analyses stratified by genetic predisposition, comorbidities, and sex hormones were performed."1.72Sex-specific association between coffee consumption and incident chronic kidney disease: a population-based analysis of 359,906 participants from the UK Biobank. ( Chen, W; Fu, P; Hu, Y; Li, C; Qu, Y; Song, H; Tang, L; Yang, H; Yang, L; Zeng, X; Zeng, Y, 2022)
"Caffeine intake has been inversely associated with Parkinson's disease (PD) risk."1.48Interaction between caffeine and polymorphisms of glutamate ionotropic receptor NMDA type subunit 2A (GRIN2A) and cytochrome P450 1A2 (CYP1A2) on Parkinson's disease risk. ( Ascherio, A; Betensky, RA; Gao, X; Hannan, MT; Hughes, KC; Kim, IY; McCullough, ML; O'Reilly, ÉJ; Schwarzschild, MA, 2018)
"We identified 43 malignant hyperthermia families carrying one of the six RYR1 variants."1.46Assessing the pathogenicity of RYR1 variants in malignant hyperthermia. ( Allen, PD; Bilmen, JG; Booms, P; Daly, C; Hopkins, PM; Merritt, A; Miller, DM; Shaw, MA; Steele, DS; Stowell, KM, 2017)
"Malignant hyperthermia is a life-threatening condition caused by autosomal dominant mutations in the ryanodine receptor type 1 gene."1.37Analysis of human cultured myotubes responses mediated by ryanodine receptor 1. ( Hamada, H; Kawamoto, M; Kobayashi, M; Migita, T; Mukaida, K; Yuge, O, 2011)
"Caffeine intake has been associated with a decreased risk of Parkinson's disease (PD) in men but the effect in women is less clear, and appears to be modified by use of post-menopausal estrogens."1.36Polymorphisms of caffeine metabolism and estrogen receptor genes and risk of Parkinson's disease in men and women. ( Ascherio, A; Gao, X; Palacios, N; Schwarzschild, M; Simon, K; Weisskopf, M, 2010)
"Malignant hyperthermia is a pharmacogenetic skeletal muscle disorder of intracellular calcium (Ca2+) homeostasis with an autosomal dominant inheritance."1.35Effects of propofol on calcium homeostasis in human skeletal muscle. ( Hamada, H; Kawamoto, M; Kobayashi, M; Migita, T; Mukaida, K; Nishino, I; Yuge, O, 2009)
"Roberts syndrome is an autosomal recessive disorder characterised primarily by symmetric reduction of all limbs and growth retardation."1.32Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes. ( Ascoli, C; Mariani, T; Montagna, C; Musio, A; Ried, T; Vezzoni, P; Zambroni, D, 2004)
"The caffeine ratio was statistically significantly higher in men compared to women, in smoking men and women compared to non-smoking persons of the same gender and in women not taking oral contraceptives compared with women on oral contraceptives."1.31The interindividual differences in the 3-demthylation of caffeine alias CYP1A2 is determined by both genetic and environmental factors. ( Brix, TH; Brøsen, K; Kyvik, KO; Rasmussen, BB, 2002)
"The diagnostic outcomes of tests for malignant hyperthermia susceptibility were compared between two laboratories by using muscle tissue from the same patients."1.31Between-center variability of results of the in vitro contracture test for malignant hyperthermia susceptibility. ( Bendixen, D; Islander, G; Ording, H; Ranklev-Twetman, E, 2000)
"Central core disease (CCD) and nemaline myopathy (NM) are congenital myopathies for which differential diagnosis is often based on the presence either of cores or rods."1.31An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor. ( Fardeau, M; Lerale, J; Lunardi, J; MacLennan, DH; Monnier, N; Nivoche, Y; Qi, D; Romero, NB, 2000)
"Xenon 70% did not cause an increase in baseline tension of any MH-susceptible muscle specimen in contrast to halothane and caffeine."1.31Xenon does not induce contracture in human malignant hyperthermia muscle. ( Baur, CP; Froeba, G; Georgieff, M; Jurkat-Rott, K; Klingler, W; Lehmann-Horn, F; Marx, T; Schoch, E, 2000)
"The determination of susceptibility to malignant hyperthermia (MH) by genetic investigation is a controversial issue because of the genetic heterogeneity of this disorder."1.31Homozygous and heterozygous Arg614Cys mutations (1840C-->T) in the ryanodine receptor gene co-segregate with malignant hyperthermia susceptibility in a German family. ( Deutrich, C; Froster, UG; Olthoff, D; Rueffert, H; Thamm, B, 2001)
"Caffeine is an addictive psychoactive substance."1.30Caffeine intake, tolerance, and withdrawal in women: a population-based twin study. ( Kendler, KS; Prescott, CA, 1999)
"Malignant hyperthermia is a potentially fatal pharmacogenetic disorder triggered by volatile anesthetics (halothane, enflurane, isoflurane) and/or succinylcholine."1.28[Diagnosis of susceptibility for malignant hyperthermia using in-vitro muscle contraction testing in Switzerland]. ( Censier, K; Drewe, J; Frei, F; Rothenbühler, JM; Seeberger, MD; Urwyler, A, 1991)

Research

Studies (80)

TimeframeStudies, this research(%)All Research%
pre-19901 (1.25)18.7374
1990's11 (13.75)18.2507
2000's31 (38.75)29.6817
2010's34 (42.50)24.3611
2020's3 (3.75)2.80

Authors

AuthorsStudies
Tang, L1
Yang, L1
Chen, W1
Li, C1
Zeng, Y1
Yang, H1
Hu, Y1
Qu, Y1
Song, H1
Zeng, X1
Fu, P1
Drogou, C1
Erblang, M1
Metlaine, A1
Berot, S1
Derbois, C1
Olaso, R1
Boland, A1
Deleuze, JF1
Thomas, C1
Léger, D1
Chennaoui, M1
Sauvet, F1
Gomez-Merino, D1
Wren, LM1
DeKeyser, JM1
Barefield, DY1
Hawkins, NA1
McNally, EM1
Kearney, JA1
Wasserstrom, JA1
George, AL1
Findley, AS1
Richards, AL1
Petrini, C1
Alazizi, A1
Doman, E1
Shanku, AG1
Davis, GO1
Hauff, N1
Sorokin, Y1
Wen, X1
Pique-Regi, R1
Luca, F1
Simon, DK1
Wu, C1
Tilley, BC1
Lohmann, K1
Klein, C1
Payami, H2
Wills, AM1
Aminoff, MJ1
Bainbridge, J1
Dewey, R1
Hauser, RA1
Schaake, S1
Schneider, JS1
Sharma, S1
Singer, C1
Tanner, CM2
Truong, D1
Wei, P1
Wong, PS1
Yang, T1
Merritt, A1
Booms, P2
Shaw, MA3
Miller, DM1
Daly, C1
Bilmen, JG1
Stowell, KM2
Allen, PD2
Steele, DS2
Hopkins, PM4
Michelucci, A1
Paolini, C1
Boncompagni, S1
Canato, M1
Reggiani, C1
Protasi, F1
Kim, IY1
O'Reilly, ÉJ1
Hughes, KC1
Gao, X2
Schwarzschild, MA1
McCullough, ML1
Hannan, MT1
Betensky, RA1
Ascherio, A2
Kondo, T1
Yasuda, T1
Mukaida, K3
Otsuki, S1
Kanzaki, R1
Miyoshi, H1
Hamada, H3
Nishino, I2
Kawamoto, M3
Cornelis, MC3
Munafo, MR1
Orlov, D1
Keith, J1
Rosen, D1
Croul, S1
Kraeva, N1
Riazi, S1
Le Guen, M1
Houissa, H1
Langeron, O1
Dik, VK1
Bueno-de-Mesquita, HB1
Van Oijen, MG1
Siersema, PD1
Uiterwaal, CS1
Van Gils, CH1
Van Duijnhoven, FJ1
Cauchi, S1
Yengo, L1
Froguel, P1
Overvad, K1
Bech, BH1
Tjønneland, A1
Olsen, A1
Boutron-Ruault, MC1
Racine, A1
Fagherazzi, G1
Kühn, T1
Campa, D1
Boeing, H1
Aleksandrova, K1
Trichopoulou, A1
Peppa, E1
Oikonomou, E1
Palli, D1
Grioni, S1
Vineis, P1
Tumino, R1
Panico, S1
Peeters, PH1
Weiderpass, E1
Engeset, D1
Braaten, T1
Dorronsoro, M1
Chirlaque, MD1
Sánchez, MJ1
Barricarte, A1
Zamora-Ros, R1
Argüelles, M1
Jirström, K1
Wallström, P1
Nilsson, LM1
Ljuslinder, I1
Travis, RC1
Khaw, KT1
Wareham, N1
Freisling, H1
Licaj, I1
Jenab, M1
Gunter, MJ1
Murphy, N1
Romaguera-Bosch, D1
Riboli, E1
Kiyohara, C2
Washio, M1
Horiuchi, T1
Asami, T1
Ide, S1
Atsumi, T1
Kobashi, G1
Takahashi, H1
Tada, Y1
Yamada-Fowler, N1
Fredrikson, M1
Söderkvist, P1
Palatini, P1
Benetti, E1
Mos, L1
Garavelli, G1
Mazzer, A1
Cozzio, S1
Fania, C1
Casiglia, E1
Imene, A1
Maurice, AJ1
Arij, M1
Sofia, P1
Saad, S1
Kumar, PM1
Paing, SS1
Li, H1
Pavanni, R1
Yuen, Y1
Zhao, Y1
Tan, EK1
Johannsen, S1
Treves, S2
Müller, CR1
Mögele, S1
Schneiderbanger, D1
Roewer, N1
Schuster, F1
Quan, L1
Chattopadhyay, K1
Nelson, HH1
Chan, KK1
Xiang, YB1
Zhang, W2
Wang, R1
Gao, YT1
Yuan, JM1
Li, X1
Liang, L1
Song, F1
De Vivo, I1
Giovannucci, E1
Tang, JY1
Han, J1
Delamarre, A1
Meissner, WG1
Nunes, RA1
Mazzotti, DR1
Hirotsu, C1
Andersen, ML1
Tufik, S1
Bittencourt, L1
Kendler, KS3
Schmitt, E1
Aggen, SH1
Prescott, CA2
Facheris, MF1
Schneider, NK1
Lesnick, TG1
de Andrade, M1
Cunningham, JM1
Rocca, WA1
Maraganore, DM1
Kadlubar, S1
Anderson, JP1
Sweeney, C1
Gross, MD1
Lang, NP1
Kadlubar, FF1
Anderson, KE1
Migita, T2
Kobayashi, M2
Yuge, O2
Carpenter, D2
Robinson, RL2
Quinnell, RJ1
Ringrose, C2
Hogg, M1
Casson, F1
Iles, DE1
Halsall, PJ2
Leo, V1
Morris, A1
Palacios, N1
Weisskopf, M1
Simon, K1
Schwarzschild, M1
Yang, A1
Childs, E2
Palmer, AA1
de Wit, H2
Mellick, GD1
Ross, OA1
Popat, RA1
Van Den Eeden, SK1
Kamel, F1
Umbach, DM1
Marder, K1
Mayeux, R1
Ritz, B1
Ross, GW1
Petrovitch, H1
Topol, B1
McGuire, V1
Costello, S1
Manthripragada, AD1
Southwick, A1
Myers, RM1
Nelson, LM1
Hill-Burns, EM1
Hamza, TH1
Zabetian, CP1
Factor, SA1
Blanco, C1
Myers, J1
Amin, N1
Byrne, E1
Johnson, J1
Chenevix-Trench, G2
Walter, S1
Nolte, IM1
Vink, JM1
Rawal, R1
Mangino, M1
Teumer, A1
Keers, JC1
Verwoert, G1
Baumeister, S1
Biffar, R1
Petersmann, A1
Dahmen, N1
Doering, A1
Isaacs, A1
Broer, L1
Wray, NR1
Montgomery, GW1
Levy, D1
Psaty, BM1
Gudnason, V1
Chakravarti, A1
Sulem, P1
Gudbjartsson, DF1
Kiemeney, LA1
Thorsteinsdottir, U1
Stefansson, K1
van Rooij, FJ1
Aulchenko, YS1
Hottenga, JJ1
Rivadeneira, FR1
Hofman, A1
Uitterlinden, AG1
Hammond, CJ1
Shin, SY1
Ikram, A1
Witteman, JC1
Janssens, AC1
Snieder, H1
Tiemeier, H1
Wolfenbuttel, BH1
Oostra, BA1
Heath, AC1
Wichmann, E1
Spector, TD1
Grabe, HJ1
Boomsma, DI1
Martin, NG1
van Duijn, CM1
Domschke, K1
Gajewska, A1
Winter, B1
Herrmann, MJ1
Warrings, B1
Mühlberger, A1
Wosnitza, K1
Glotzbach, E1
Conzelmann, A1
Dlugos, A1
Fobker, M1
Jacob, C1
Arolt, V1
Reif, A1
Pauli, P1
Zwanzger, P1
Deckert, J2
Eltit, JM1
Bannister, RA1
Moua, O1
Altamirano, F1
Pessah, IN1
Molinski, TF1
López, JR1
Beam, KG1
Johnson, JK1
Waddell, N1
Gao, J1
Nalls, MA1
Shi, M1
Joubert, BR1
Hernandez, DG1
Huang, X1
Hollenbeck, A1
Singleton, AB1
Chen, H1
Miyake, Y1
Tanaka, K1
Fukushima, W1
Sasaki, S1
Tsuboi, Y1
Yamada, T1
Oeda, T1
Shimada, H1
Kawamura, N1
Sakae, N1
Fukuyama, H1
Hirota, Y1
Nagai, M1
Rasmussen, BB1
Brix, TH1
Kyvik, KO1
Brøsen, K1
Goodman, MT1
Tung, KH1
McDuffie, K1
Wilkens, LR1
Donlon, TA1
Wehner, M1
Rueffert, H2
Koenig, F1
Olthoff, D2
Ginz, HF1
Girard, T2
Censier, K3
Urwyler, A3
Musio, A1
Mariani, T1
Montagna, C1
Zambroni, D1
Ascoli, C1
Ried, T1
Vezzoni, P1
Sata, F1
Yamada, H1
Suzuki, K1
Saijo, Y1
Kato, EH1
Morikawa, M1
Minakami, H1
Kishi, R1
Logroscino, G1
Zusterzeel, PL1
te Morsche, RH1
Raijmakers, MT1
Roes, EM1
Peters, WH1
Steegers-Theunissen, RP1
Steegers, EA1
Natarajan, TG1
Ganesan, N1
Carter-Nolan, P1
Tucker, CA1
Shields, PG1
Adams-Campbell, LL1
Kannankeril, PJ1
Mitchell, BM1
Goonasekera, SA1
Chelu, MG1
Sood, S1
Kearney, DL1
Danila, CI1
De Biasi, M1
Wehrens, XH1
Pautler, RG1
Roden, DM1
Taffet, GE1
Dirksen, RT1
Anderson, ME1
Hamilton, SL1
Islander, G4
Rydenfelt, K1
Ranklev, E1
Bodelsson, M1
Campos, H1
Baylin, A1
Bruno, MK1
Lee, HY1
Auburger, GW1
Friedman, A1
Nielsen, JE1
Lang, AE1
Bertini, E1
Van Bogaert, P1
Averyanov, Y1
Hallett, M1
Gwinn-Hardy, K1
Sorenson, B1
Pandolfo, M1
Kwiecinski, H1
Servidei, S1
Fu, YH1
Ptácek, L1
Nardi, AE1
Valença, AM1
Nascimento, I1
Freire, RC1
Veras, AB1
de-Melo-Neto, VL1
Lopes, FL1
King, AL1
Soares-Filho, GL1
Mezzasalma, MA1
Rassi, A1
Zin, WA1
El-Sohemy, A1
Hohoff, C1
Xu, K1
Badner, J1
Ortiz Gómez, JR1
Kloth, MT1
Gee, RL1
Messing, EM1
Swaminathan, S1
Owen, VJ1
Taske, NL1
Lamb, GD1
Fagerlund, TH2
Ranklev Twetman, E2
Berg, K2
Glauber, V1
Ben Abraham, R1
Zweig, A1
Perel, A1
Ording, H2
Bendixen, D2
Ceçener, G1
Egeli, U3
Taşdelen, I1
Tunca, B3
Duman, H1
Kizil, A3
Montes, A1
Ramos, R1
Trillo, L1
Silva, T1
Puig, MM1
Zorluoğlu, A2
Yilmazlar, T2
Yerci, O2
Jung, RE1
Yeo, RA1
Gangestad, SW1
Ranklev-Twetman, E1
Monnier, N1
Romero, NB1
Lerale, J1
Nivoche, Y1
Qi, D1
MacLennan, DH1
Fardeau, M1
Lunardi, J1
Baur, CP1
Klingler, W1
Jurkat-Rott, K1
Froeba, G1
Schoch, E1
Marx, T1
Georgieff, M1
Lehmann-Horn, F1
Deutrich, C1
Thamm, B1
Froster, UG1
Mueller, CR1
Zorzato, F1
Kalow, W1
Britt, BA1
Chan, FY1
Cosgrove, SB1
Eisele, PH1
Martucci, RW1
Gronert, GA1
Williams, RR1
Hunt, SC1
Hasstedt, SJ1
Hopkins, PN1
Wu, LL1
Berry, TD1
Stults, BM1
Barlow, GK1
Schumacher, MC1
Lifton, RP1
Seeberger, MD1
Drewe, J1
Rothenbühler, JM1
Frei, F1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Epidemiology of Sleep Disturbances Among the Adult Population of the Sao Paulo City[NCT00596713]1,100 participants (Actual)Observational2007-06-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

9 reviews available for caffeine and Genetic Predisposition

ArticleYear
Mendelian Randomization Studies of Coffee and Caffeine Consumption.
    Nutrients, 2018, Sep-20, Volume: 10, Issue:10

    Topics: Caffeine; Central Nervous System Stimulants; Coffee; Feeding Behavior; Genetic Predisposition to Dis

2018
DNA testing for malignant hyperthermia: the reality and the dream.
    Anesthesia and analgesia, 2014, Volume: 118, Issue:2

    Topics: Biopsy; Caffeine; Calcium Channels; Calcium Channels, L-Type; Computational Biology; Genetic Predisp

2014
Epidemiology, environmental risk factors and genetics of Parkinson's disease.
    Presse medicale (Paris, France : 1983), 2017, Volume: 46, Issue:2 Pt 1

    Topics: Age Distribution; Age of Onset; alpha-Synuclein; Caffeine; Causality; Gene-Environment Interaction;

2017
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM.
    Molecular psychiatry, 2012, Volume: 17, Issue:11

    Topics: Antigens, Neoplasm; Apoptosis Regulatory Proteins; Caffeine; Cell Adhesion Molecules; Cell Line; Cof

2012
The role of early life environmental risk factors in Parkinson disease: what is the evidence?
    Environmental health perspectives, 2005, Volume: 113, Issue:9

    Topics: Age Factors; Animals; Caffeine; Coffee; Environmental Exposure; Genetic Predisposition to Disease; H

2005
Coffee consumption and risk of type 2 diabetes and heart disease.
    Nutrition reviews, 2007, Volume: 65, Issue:4

    Topics: Caffeine; Coffee; Diabetes Mellitus, Type 2; Evidence-Based Medicine; Genetic Predisposition to Dise

2007
Coffee, caffeine, and coronary heart disease.
    Current opinion in clinical nutrition and metabolic care, 2007, Volume: 10, Issue:6

    Topics: Beverages; Blood Pressure; Caffeine; Cholesterol; Coffee; Coronary Disease; Dose-Response Relationsh

2007
[Anesthesia in malignant hyperthermia].
    Revista espanola de anestesiologia y reanimacion, 2008, Volume: 55, Issue:3

    Topics: Adolescent; Adult; Aged; Anesthetics, Inhalation; Caffeine; Calcium Signaling; Child; Child, Prescho

2008
Epidemiology and inheritance of malignant hyperthermia.
    International anesthesiology clinics, 1979,Winter, Volume: 17, Issue:4

    Topics: Adenosine Triphosphate; Caffeine; Creatine Kinase; Female; Genetic Predisposition to Disease; Haloth

1979

Trials

4 trials available for caffeine and Genetic Predisposition

ArticleYear
Modifying effect of N-acetyltransferase 2 genotype on the association between systemic lupus erythematosus and consumption of alcohol and caffeine-rich beverages.
    Arthritis care & research, 2014, Volume: 66, Issue:7

    Topics: Adult; Alcohol Drinking; Arylamine N-Acetyltransferase; Asian People; Beverages; Caffeine; Case-Cont

2014
A caffeine challenge test in panic disorder patients, their healthy first-degree relatives, and healthy controls.
    Depression and anxiety, 2008, Volume: 25, Issue:10

    Topics: Adult; Arousal; Caffeine; Central Nervous System Stimulants; Citrates; Double-Blind Method; Female;

2008
Developmental instability predicts individual variation in verbal memory skill after caffeine ingestion.
    Neuropsychiatry, neuropsychology, and behavioral neurology, 2000, Volume: 13, Issue:3

    Topics: Abnormalities, Multiple; Adolescent; Adult; Biomarkers; Caffeine; Central Nervous System Stimulants;

2000
Genotype-phenotype comparison of the Swiss malignant hyperthermia population.
    Human mutation, 2001, Volume: 18, Issue:4

    Topics: Caffeine; DNA Mutational Analysis; Gene Frequency; Genetic Heterogeneity; Genetic Predisposition to

2001

Other Studies

67 other studies available for caffeine and Genetic Predisposition

ArticleYear
Sex-specific association between coffee consumption and incident chronic kidney disease: a population-based analysis of 359,906 participants from the UK Biobank.
    Chinese medical journal, 2022, Jun-20, Volume: 135, Issue:12

    Topics: Bayes Theorem; Biological Specimen Banks; Caffeine; Coffee; Female; Genetic Predisposition to Diseas

2022
Relationship between genetic polymorphisms of cytokines and self-reported sleep complaints and habitual caffeine consumption.
    Sleep medicine, 2023, Volume: 101

    Topics: Caffeine; Cross-Sectional Studies; Cytokines; Genetic Predisposition to Disease; Genotype; Humans; P

2023
Sex and Gene Influence Arrhythmia Susceptibility in Murine Models of Calmodulinopathy.
    Circulation. Arrhythmia and electrophysiology, 2023, Volume: 16, Issue:9

    Topics: Animals; Arrhythmias, Cardiac; Caffeine; Calmodulin; Disease Models, Animal; Epinephrine; Female; Ge

2023
Interpreting Coronary Artery Disease Risk Through Gene-Environment Interactions in Gene Regulation.
    Genetics, 2019, Volume: 213, Issue:2

    Topics: Caffeine; Coronary Artery Disease; Endothelial Cells; Gene Expression Regulation; Gene-Environment I

2019
Caffeine, creatine, GRIN2A and Parkinson's disease progression.
    Journal of the neurological sciences, 2017, Apr-15, Volume: 375

    Topics: Aged; Caffeine; Creatine; Disease Progression; Female; Gene-Environment Interaction; Genetic Predisp

2017
Assessing the pathogenicity of RYR1 variants in malignant hyperthermia.
    British journal of anaesthesia, 2017, Apr-01, Volume: 118, Issue:4

    Topics: Caffeine; Calcium; Cloning, Molecular; Family; Genetic Predisposition to Disease; Genetic Variation;

2017
Strenuous exercise triggers a life-threatening response in mice susceptible to malignant hyperthermia.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2017, Volume: 31, Issue:8

    Topics: Animals; Caffeine; Calcium-Binding Proteins; Calsequestrin; Electric Stimulation; Gene Expression Re

2017
Interaction between caffeine and polymorphisms of glutamate ionotropic receptor NMDA type subunit 2A (GRIN2A) and cytochrome P450 1A2 (CYP1A2) on Parkinson's disease risk.
    Movement disorders : official journal of the Movement Disorder Society, 2018, Volume: 33, Issue:3

    Topics: Caffeine; Case-Control Studies; Cohort Studies; Cytochrome P-450 CYP1A2; Female; Gene Frequency; Gen

2018
Genetic and functional analysis of the RYR1 mutation p.Thr84Met revealed a susceptibility to malignant hyperthermia.
    Journal of anesthesia, 2018, Volume: 32, Issue:2

    Topics: Animals; Caffeine; Calcium; Child; Cresols; Genetic Predisposition to Disease; HEK293 Cells; Humans;

2018
Analysis of histomorphology in malignant hyperthermia-susceptible patients.
    Canadian journal of anaesthesia = Journal canadien d'anesthesie, 2013, Volume: 60, Issue:10

    Topics: Adult; Caffeine; Female; Follow-Up Studies; Genetic Predisposition to Disease; Genotype; Halothane;

2013
[Malignant hyperthermia: multifactorial events leading to a crisis].
    Annales francaises d'anesthesie et de reanimation, 2013, Volume: 32, Issue:11

    Topics: Accidents, Traffic; Algorithms; Bicycling; Biopsy; Caffeine; Central Nervous System Stimulants; Gene

2013
Coffee and tea consumption, genotype-based CYP1A2 and NAT2 activity and colorectal cancer risk-results from the EPIC cohort study.
    International journal of cancer, 2014, Jul-15, Volume: 135, Issue:2

    Topics: Adult; Aged; Arylamine N-Acetyltransferase; Caffeine; Case-Control Studies; Coffee; Cohort Studies;

2014
Caffeine interaction with glutamate receptor gene GRIN2A: Parkinson's disease in Swedish population.
    PloS one, 2014, Volume: 9, Issue:6

    Topics: Aged; Aged, 80 and over; Caffeine; Case-Control Studies; Female; Gene Frequency; Genetic Predisposit

2014
Association of coffee consumption and CYP1A2 polymorphism with risk of impaired fasting glucose in hypertensive patients.
    European journal of epidemiology, 2015, Volume: 30, Issue:3

    Topics: Adolescent; Adult; Blood Glucose; Caffeine; Coffee; Cytochrome P-450 CYP1A2; Female; Follow-Up Studi

2015
Breast Cancer Association with CYP1A2 Activity and Gene Polymorphisms--a Preliminary Case-control Study in Tunisia.
    Asian Pacific journal of cancer prevention : APJCP, 2015, Volume: 16, Issue:8

    Topics: Breast Neoplasms; Caffeine; Case-Control Studies; Cytochrome P-450 CYP1A2; Female; Genetic Predispos

2015
Differential effect of caffeine intake in subjects with genetic susceptibility to Parkinson's Disease.
    Scientific reports, 2015, Nov-02, Volume: 5

    Topics: Adult; Aged; Aged, 80 and over; Caffeine; Case-Control Studies; Drinking; Female; Gene Frequency; Ge

2015
Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia.
    Neuromuscular disorders : NMD, 2016, Volume: 26, Issue:1

    Topics: Anesthetics; Arginine; B-Lymphocytes; Caffeine; Cell Line, Transformed; Cresols; Family Health; Fema

2016
Differential association for N-acetyltransferase 2 genotype and phenotype with bladder cancer risk in Chinese population.
    Oncotarget, 2016, Jun-28, Volume: 7, Issue:26

    Topics: Aged; Arylamine N-Acetyltransferase; Asian People; Caffeine; Carcinogens; Case-Control Studies; Chin

2016
A genome-wide analysis of gene-caffeine consumption interaction on basal cell carcinoma.
    Carcinogenesis, 2016, Volume: 37, Issue:12

    Topics: Animals; Ataxia Telangiectasia Mutated Proteins; Caffeine; Carcinogenesis; Carcinoma, Basal Cell; Ep

2016
The association between caffeine consumption and objective sleep variables is dependent on ADORA2A c.1083T>C genotypes.
    Sleep medicine, 2017, Volume: 30

    Topics: Adult; Aged; Aged, 80 and over; Caffeine; Central Nervous System Stimulants; Female; Genetic Predisp

2017
Genetic and environmental influences on alcohol, caffeine, cannabis, and nicotine use from early adolescence to middle adulthood.
    Archives of general psychiatry, 2008, Volume: 65, Issue:6

    Topics: Adolescent; Adult; Age Factors; Alcoholism; Caffeine; Central Nervous System Stimulants; Child; Dise

2008
Coffee, caffeine-related genes, and Parkinson's disease: a case-control study.
    Movement disorders : official journal of the Movement Disorder Society, 2008, Oct-30, Volume: 23, Issue:14

    Topics: Adult; Aged; Aged, 80 and over; Caffeine; Case-Control Studies; Coffee; Cytochrome P-450 CYP1A2; DNA

2008
Phenotypic CYP2A6 variation and the risk of pancreatic cancer.
    JOP : Journal of the pancreas, 2009, May-18, Volume: 10, Issue:3

    Topics: Adult; Aged; Aged, 80 and over; Aryl Hydrocarbon Hydroxylases; Caffeine; Carcinogens; Case-Control S

2009
Effects of propofol on calcium homeostasis in human skeletal muscle.
    Anaesthesia and intensive care, 2009, Volume: 37, Issue:3

    Topics: Adolescent; Adult; Aged; Anesthetics, Intravenous; Caffeine; Calcium; Child; Child, Preschool; Dose-

2009
Genetic variation in RYR1 and malignant hyperthermia phenotypes.
    British journal of anaesthesia, 2009, Volume: 103, Issue:4

    Topics: Anesthetics, Inhalation; Caffeine; Creatine Kinase; DNA Mutational Analysis; DNA, Complementary; Fem

2009
The role of CACNA1S in predisposition to malignant hyperthermia.
    BMC medical genetics, 2009, Oct-13, Volume: 10

    Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Caffeine; Calcium Channels; Calcium Channels, L-Type;

2009
Polymorphisms of caffeine metabolism and estrogen receptor genes and risk of Parkinson's disease in men and women.
    Parkinsonism & related disorders, 2010, Volume: 16, Issue:6

    Topics: Caffeine; Case-Control Studies; Cytochrome P-450 CYP1A2; Estrogen Replacement Therapy; Female; Genet

2010
More on ADORA.
    Psychopharmacology, 2010, Volume: 212, Issue:4

    Topics: Anxiety; Caffeine; Central Nervous System Stimulants; Coffee; Drinking Behavior; Feeding Behavior; G

2010
Caffeine and Parkinson's disease: are we getting our fix on risk-modifying gene-environment interactions?
    European journal of neurology, 2011, Volume: 18, Issue:5

    Topics: Caffeine; Cytochrome P-450 CYP1A2; Female; Genetic Predisposition to Disease; Humans; Male; Neuropro

2011
Coffee, ADORA2A, and CYP1A2: the caffeine connection in Parkinson's disease.
    European journal of neurology, 2011, Volume: 18, Issue:5

    Topics: Aged; Caffeine; Case-Control Studies; Cohort Studies; Cytochrome P-450 CYP1A2; Female; Genetic Predi

2011
Analysis of human cultured myotubes responses mediated by ryanodine receptor 1.
    Anaesthesia and intensive care, 2011, Volume: 39, Issue:2

    Topics: Adolescent; Adult; Aged; Caffeine; Calcium; Cells, Cultured; Child; Child, Preschool; Cresols; Dose-

2011
An attempt to replicate interaction between coffee and CYP1A2 gene in connection to Parkinson's disease.
    European journal of neurology, 2011, Volume: 18, Issue:9

    Topics: Caffeine; Cytochrome P-450 CYP1A2; Female; Genetic Predisposition to Disease; Humans; Male; Neuropro

2011
Gambling, disordered gambling and their association with major depression and substance use: a web-based cohort and twin-sibling study.
    Psychological medicine, 2012, Volume: 42, Issue:3

    Topics: Adult; Alcohol Drinking; Behavior, Addictive; Caffeine; Cohort Studies; Depressive Disorder, Major;

2012
ADORA2A Gene variation, caffeine, and emotional processing: a multi-level interaction on startle reflex.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2012, Volume: 37, Issue:3

    Topics: Adult; Anxiety; Caffeine; Double-Blind Method; Emotions; Female; Genetic Predisposition to Disease;

2012
Malignant hyperthermia susceptibility arising from altered resting coupling between the skeletal muscle L-type Ca2+ channel and the type 1 ryanodine receptor.
    Proceedings of the National Academy of Sciences of the United States of America, 2012, May-15, Volume: 109, Issue:20

    Topics: Analysis of Variance; Anesthetics; Body Temperature; Caffeine; Calcium; Caveolin 1; DNA, Complementa

2012
The application of nonsense-mediated mRNA decay inhibition to the identification of breast cancer susceptibility genes.
    BMC cancer, 2012, Jun-15, Volume: 12

    Topics: Base Sequence; Breast Neoplasms; Caffeine; Cell Line, Tumor; Family; Female; Gene Expression Profili

2012
An exploratory analysis on gene-environment interactions for Parkinson disease.
    Neurobiology of aging, 2012, Volume: 33, Issue:10

    Topics: Age of Onset; Aged; Caffeine; Female; Gene-Environment Interaction; Genetic Loci; Genetic Predisposi

2012
Lack of association between BST1 polymorphisms and sporadic Parkinson's disease in a Japanese population.
    Journal of the neurological sciences, 2012, Dec-15, Volume: 323, Issue:1-2

    Topics: ADP-ribosyl Cyclase; Age of Onset; Aged; Antigens, CD; Asian People; Caffeine; Case-Control Studies;

2012
The interindividual differences in the 3-demthylation of caffeine alias CYP1A2 is determined by both genetic and environmental factors.
    Pharmacogenetics, 2002, Volume: 12, Issue:6

    Topics: Adolescent; Adult; Biotransformation; Caffeine; Central Nervous System Stimulants; Chromatography, H

2002
Association of caffeine intake and CYP1A2 genotype with ovarian cancer.
    Nutrition and cancer, 2003, Volume: 46, Issue:1

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Caffeine; Case-Control Studies; Confidence Intervals; Cy

2003
Calcium release from sarcoplasmic reticulum is facilitated in human myotubes derived from carriers of the ryanodine receptor type 1 mutations Ile2182Phe and Gly2375Ala.
    Genetic testing, 2003,Fall, Volume: 7, Issue:3

    Topics: Adult; Aged; Caffeine; Calcium; Child; Child, Preschool; Cresols; Female; Genetic Predisposition to

2003
Similar susceptibility to halothane, caffeine and ryanodine in vitro reflects pharmacogenetic variability of malignant hyperthermia.
    European journal of anaesthesiology, 2004, Volume: 21, Issue:2

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anesthetics, Inhalation; Biopsy; Caffeine; Central Nervo

2004
Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes.
    Gene, 2004, Apr-28, Volume: 331

    Topics: Abnormalities, Multiple; Aneuploidy; Caffeine; Cell Cycle; Cell Division; Cell Line; Centromere; Chr

2004
Caffeine intake, CYP1A2 polymorphism and the risk of recurrent pregnancy loss.
    Molecular human reproduction, 2005, Volume: 11, Issue:5

    Topics: Abortion, Habitual; Adult; Alleles; Caffeine; Case-Control Studies; Cytochrome P-450 CYP1A2; Female;

2005
N-acetyl-transferase phenotype and risk for preeclampsia.
    American journal of obstetrics and gynecology, 2005, Volume: 193, Issue:3 Pt 1

    Topics: Adult; Arylamine N-Acetyltransferase; Caffeine; Female; Genetic Predisposition to Disease; HELLP Syn

2005
gamma-Radiation-induced chromosomal mutagen sensitivity is associated with breast cancer risk in African-American women: caffeine modulates the outcome of mutagen sensitivity assay.
    Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2006, Volume: 15, Issue:3

    Topics: Adult; Age Distribution; Aged; Aged, 80 and over; Biomarkers, Tumor; Black or African American; Brea

2006
Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathy.
    Proceedings of the National Academy of Sciences of the United States of America, 2006, Aug-08, Volume: 103, Issue:32

    Topics: Animals; Caffeine; Cardiomyopathies; Catecholamines; Central Nervous System Stimulants; Epinephrine;

2006
Male preponderance of patients testing positive for malignant hyperthermia susceptibility.
    Acta anaesthesiologica Scandinavica, 2007, Volume: 51, Issue:5

    Topics: Caffeine; Family; Female; Genetic Predisposition to Disease; Halothane; Humans; Male; Malignant Hype

2007
Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia.
    Neurology, 2007, May-22, Volume: 68, Issue:21

    Topics: Adolescent; Adult; Age of Onset; Caffeine; Child; Child, Preschool; Chorea; DNA Mutational Analysis;

2007
Association between ADORA2A and DRD2 polymorphisms and caffeine-induced anxiety.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2008, Volume: 33, Issue:12

    Topics: Adenosine; Adolescent; Adult; Anxiety Disorders; Brain; Brain Chemistry; Caffeine; DNA Mutational An

2008
Expression of N-acetyltransferase (NAT) in cultured human uroepithelial cells.
    Carcinogenesis, 1994, Volume: 15, Issue:12

    Topics: Acetylation; Adult; Alleles; Amines; Arylamine N-Acetyltransferase; Biomarkers; Caffeine; Cells, Cul

1994
Reduced Mg2+ inhibition of Ca2+ release in muscle fibers of pigs susceptible to malignant hyperthermia.
    The American journal of physiology, 1997, Volume: 272, Issue:1 Pt 1

    Topics: Animals; Caffeine; Calcium; Calcium Channel Blockers; Dantrolene; Genetic Predisposition to Disease;

1997
Malignant hyperthermia susceptibility, an autosomal dominant disorder?
    Clinical genetics, 1997, Volume: 51, Issue:6

    Topics: Adolescent; Adult; Caffeine; Calcium Channels; Child; Child, Preschool; Female; Genes, Dominant; Gen

1997
The Israeli Diagnostic Center for Malignant Hyperthermia: 7-years' accumulated experience.
    Israel journal of medical sciences, 1997, Volume: 33, Issue:10

    Topics: Academies and Institutes; Adult; Aged; Biopsy; Caffeine; Child; Electromyography; Female; Genetic Pr

1997
Discordance between malignant hyperthermia susceptibility and RYR1 mutation C1840T in two Scandinavian MH families exhibiting this mutation.
    Clinical genetics, 1997, Volume: 52, Issue:6

    Topics: Anesthesia; Caffeine; Denmark; Female; Genetic Predisposition to Disease; Halothane; Humans; Male; M

1997
Caffeine intake, tolerance, and withdrawal in women: a population-based twin study.
    The American journal of psychiatry, 1999, Volume: 156, Issue:2

    Topics: Adult; Caffeine; Carbonated Beverages; Coffee; Diseases in Twins; Drug Overdose; Drug Tolerance; Fem

1999
Common fragile site expression and genetic predisposition to breast cancer.
    Teratogenesis, carcinogenesis, and mutagenesis, 1998, Volume: 18, Issue:6

    Topics: Aphidicolin; Breast Neoplasms; Caffeine; Chromosome Aberrations; Chromosome Fragile Sites; Chromosom

1998
[Malignant hyperthermia: difficulty in diagnosing susceptibility in Spain].
    Revista espanola de anestesiologia y reanimacion, 1999, Volume: 46, Issue:3

    Topics: Anesthetics, Inhalation; Caffeine; Europe; Genetic Predisposition to Disease; Halothane; Humans; Inf

1999
The expression of fragile sites in lymphocytes of patients with rectum cancer and their first-degree relatives.
    Cancer letters, 2000, May-01, Volume: 152, Issue:2

    Topics: Adult; Aged; Aphidicolin; Bromodeoxyuridine; Caffeine; Case-Control Studies; Cells, Cultured; Chromo

2000
The expression frequency of common fragile sites and genetic predisposition to colon cancer.
    Cancer genetics and cytogenetics, 2000, Volume: 119, Issue:2

    Topics: Adenocarcinoma; Adolescent; Adult; Aged; Alu Elements; Aphidicolin; Bromodeoxyuridine; Caffeine; Chi

2000
Between-center variability of results of the in vitro contracture test for malignant hyperthermia susceptibility.
    Anesthesia and analgesia, 2000, Volume: 91, Issue:2

    Topics: Adolescent; Adult; Aged; Anesthetics, Inhalation; Biopsy; Caffeine; Female; Genetic Predisposition t

2000
An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor.
    Human molecular genetics, 2000, Nov-01, Volume: 9, Issue:18

    Topics: Amino Acid Substitution; Caffeine; Calcium; Cell Line; DNA Mutational Analysis; Female; France; Gene

2000
Xenon does not induce contracture in human malignant hyperthermia muscle.
    British journal of anaesthesia, 2000, Volume: 85, Issue:5

    Topics: Anesthetics, Inhalation; Caffeine; Culture Techniques; Dose-Response Relationship, Drug; Drug Evalua

2000
Homozygous and heterozygous Arg614Cys mutations (1840C-->T) in the ryanodine receptor gene co-segregate with malignant hyperthermia susceptibility in a German family.
    British journal of anaesthesia, 2001, Volume: 87, Issue:2

    Topics: Adult; Anesthetics, Inhalation; Caffeine; DNA Mutational Analysis; Female; Genetic Predisposition to

2001
Evaluation of greyhound susceptibility to malignant hyperthermia using halothane-succinylcholine anesthesia and caffeine-halothane muscle contractures.
    Laboratory animal science, 1992, Volume: 42, Issue:5

    Topics: Anesthesia, Inhalation; Animals; Caffeine; Disease Susceptibility; Dog Diseases; Dogs; Genetic Predi

1992
Are there interactions and relations between genetic and environmental factors predisposing to high blood pressure?
    Hypertension (Dallas, Tex. : 1979), 1991, Volume: 18, Issue:3 Suppl

    Topics: Alcohol Drinking; Caffeine; Educational Status; Exercise; Genes; Genetic Predisposition to Disease;

1991
[Diagnosis of susceptibility for malignant hyperthermia using in-vitro muscle contraction testing in Switzerland].
    Schweizerische medizinische Wochenschrift, 1991, Apr-20, Volume: 121, Issue:16

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Biopsy; Caffeine; Child; Female; Genetic Predisposition

1991