Page last updated: 2024-10-21

1-anilino-8-naphthalenesulfonate and Cardiovascular Diseases

1-anilino-8-naphthalenesulfonate has been researched along with Cardiovascular Diseases in 67 studies

1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.

Cardiovascular Diseases: Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM.

Research Excerpts

ExcerptRelevanceReference
"To evaluate serum amylase and lipase levels and the rate of acute pancreatitis in patients with type 2 diabetes and high cardiovascular risk randomized to liraglutide or placebo and observed for 3."9.24Amylase, Lipase, and Acute Pancreatitis in People With Type 2 Diabetes Treated With Liraglutide: Results From the LEADER Randomized Trial. ( Buse, JB; Ghorbani, MLM; Nauck, MA; Steinberg, WM; Ørsted, DD, 2017)
"This study demonstrates the effectiveness of an intervention combining orlistat and lifestyle modification with Mexican-American women, a population with substantial risk for obesity."9.10Weight loss in obese Mexican Americans treated for 1-year with orlistat and lifestyle modification. ( Balasubramanyam, A; Foreyt, JP; Haddock, CK; Poston, WS; Reeves, RS; Satterwhite, O; Stormer, S; Taylor, JE, 2003)
"Orlistat was well tolerated."6.71The ORLIstat and CArdiovascular risk profile in patients with metabolic syndrome and type 2 DIAbetes (ORLICARDIA) Study. ( Athyros, VG; Bousboulas, SH; Didangelos, TP; Dimitriou, KC; Karamanos, BG; Karamitsos, DT; Pappas, SI; Sambanis, CL; Spanou, EA; Thanopoulou, AK, 2004)
"To evaluate serum amylase and lipase levels and the rate of acute pancreatitis in patients with type 2 diabetes and high cardiovascular risk randomized to liraglutide or placebo and observed for 3."5.24Amylase, Lipase, and Acute Pancreatitis in People With Type 2 Diabetes Treated With Liraglutide: Results From the LEADER Randomized Trial. ( Buse, JB; Ghorbani, MLM; Nauck, MA; Steinberg, WM; Ørsted, DD, 2017)
"This study demonstrates the effectiveness of an intervention combining orlistat and lifestyle modification with Mexican-American women, a population with substantial risk for obesity."5.10Weight loss in obese Mexican Americans treated for 1-year with orlistat and lifestyle modification. ( Balasubramanyam, A; Foreyt, JP; Haddock, CK; Poston, WS; Reeves, RS; Satterwhite, O; Stormer, S; Taylor, JE, 2003)
"Two-year treatment with orlistat plus diet significantly promotes weight loss, lessens weight regain, and improves some obesity-related disease risk factors."5.09Weight control and risk factor reduction in obese subjects treated for 2 years with orlistat: a randomized controlled trial. ( Chung, J; Davidson, MH; DiGirolamo, M; Foreyt, JP; Halsted, CH; Hauptman, J; Heber, D; Heimburger, DC; Heymsfield, SB; Lucas, CP; Robbins, DC, 1999)
"The use of orlistat during periods of attempted weight maintenance minimizes weight readjustment and facilitates long-term improvement in obesity-related disease risk factors."5.09Orlistat, a lipase inhibitor, for weight maintenance after conventional dieting: a 1-y study. ( Anderson, JW; Aronne, LJ; Fujioka, K; Hauptman, J; Hill, JO; O'Neil, PM; Smith, DK; Zavoral, JH, 1999)
" Sixty-eight women in pre-menopause (PMW) and 216 in post-menopause (POMW) were recruited; eighty-three had undergone HRT for at least 12 months, where 48 received conjugated estrogens alone (EHRT) and 35 received conjugated estrogen and medroxyprogesterone acetate (CHRT)."3.77Post-menopausal hormone therapy reduces autoantibodies to oxidized apolipoprotein B100. ( Castanho, VS; de Faria, EC; Gidlund, M; Nakamura, R, 2011)
"MAFLD is closely intertwined with type 2 diabetes, obesity, dyslipidaemia, all linked to a rise in the risk of cardiovascular disease (CVDs)."2.72Nonalcoholic fatty liver disease or metabolic dysfunction-associated fatty liver disease diagnoses and cardiovascular diseases: From epidemiology to drug approaches. ( Corsini, A; Dongiovanni, P; Paolini, E; Ruscica, M; Sirtori, CR, 2021)
"Orlistat was well tolerated."2.71The ORLIstat and CArdiovascular risk profile in patients with metabolic syndrome and type 2 DIAbetes (ORLICARDIA) Study. ( Athyros, VG; Bousboulas, SH; Didangelos, TP; Dimitriou, KC; Karamanos, BG; Karamitsos, DT; Pappas, SI; Sambanis, CL; Spanou, EA; Thanopoulou, AK, 2004)
"Non-alcoholic fatty liver disease (NAFLD) is highly prevalent among individuals with type 2 diabetes."2.66Non-alcoholic fatty liver disease and cardiovascular disease: assessing the evidence for causality. ( Brouwers, MCGJ; Isaacs, A; Simons, N; Stehouwer, CDA, 2020)
"Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in Western countries and expose patients to increased risk of hepatic and cardiovascular (CV) morbidity and mortality."2.66Nutrients, Genetic Factors, and Their Interaction in Non-Alcoholic Fatty Liver Disease and Cardiovascular Disease. ( Fargion, S; Fracanzani, AL; Iuculano, F; Lombardi, R; Pallini, G, 2020)
"In some patients with NAFLD, isolated steatosis can progress to advanced stages with non-alcoholic steatohepatitis (NASH) and fibrosis, increasing the risk of cirrhosis and hepatocellular carcinoma."2.61Non-alcoholic fatty liver disease: causes, diagnosis, cardiometabolic consequences, and treatment strategies. ( Cusi, K; Häring, HU; Stefan, N, 2019)
"Posttransplant metabolic syndrome is a common occurrence that increases the risk of steatosis in the graft liver."2.58Nonalcoholic Fatty Liver Disease/Nonalcoholic Steatohepatitis in Liver Transplantation. ( Carter, D; Chang, C; Dieterich, DT, 2018)
"The characteristic dyslipidemia of insulin resistance consists of elevated triglyceride and triglyceride-rich lipoprotein levels, low levels of high-density lipoprotein cholesterol, and increased concentrations of small, dense low-density lipoprotein cholesterol."2.41Pathophysiology and treatment of the dyslipidemia of insulin resistance. ( Capuzzi , DM; Cohn, G; Valdes, G, 2001)
"Orlistat is a new inhibitor of pancreatic lipase enzyme."2.40New aspects in the management of obesity: operation and the impact of lipase inhibitors. ( Uusitupa, M, 1999)
"To investigate the effects of the NAFLD risk alleles on the all-cause and cause-specific mortality in 5581 Chinese adults."1.72NAFLD-related gene polymorphisms and all-cause and cause-specific mortality in an Asian population: the Shanghai Changfeng Study. ( Aleteng, Q; Chen, L; Gao, X; Ge, J; He, W; Hu, Y; Huang, Q; Li, Q; Li, X; Lin, H; Ma, H; Ma, S; Pan, B; Tang, H; Wang, S; Wu, L; Wu, Q; Xia, M; Xu, W; Zeng, H; Zheng, Y, 2022)
"Fatty liver is a potentially preventable cause of serious liver diseases."1.43Childhood predictors of adult fatty liver. The Cardiovascular Risk in Young Finns Study. ( Ahola-Olli, A; Hutri-Kähönen, N; Jokinen, E; Jula, A; Juonala, M; Kähönen, M; Laitinen, T; Lehtimäki, T; Loo, BM; Mikkilä, V; Oikonen, M; Parkkola, R; Pitkänen, N; Raitakari, OT; Suomela, E; Taittonen, L; Telama, R; Tossavainen, P; Viikari, JSA; Virtanen, J, 2016)
"Metabolic syndrome was defined according to ATPIII modified criteria."1.40Non-alcoholic fatty liver disease, metabolic syndrome and patatin-like phospholipase domain-containing protein3 gene variants. ( Angelico, F; Arca, M; Baratta, F; Brancorsini, M; D'Erasmo, L; Del Ben, M; Di Costanzo, A; Loffredo, L; Pastori, D; Pignatelli, P; Polimeni, L; Violi, F, 2014)
"The higher hepatic lipase activity in NAFLD patients contributes to a more atherogenic profile linked to increased cardiovascular risk, beyond the insulin resistance and the reduction in adiponectin."1.38Hepatic lipase activity is increased in non-alcoholic fatty liver disease beyond insulin resistance. ( Berg, G; Cacciagiú, L; Fassio, E; Gonzalez Ballerga, E; Lopez, G; Lucero, D; Miksztowicz, V; Schreier, L; Sordá, J; Zago, V, 2012)
"For the case-control studies, 2110 ischemic heart disease patients vs."1.35Hepatic lipase, genetically elevated high-density lipoprotein, and risk of ischemic cardiovascular disease. ( Andersen, RV; Jensen, GB; Johannsen, TH; Kamstrup, PR; Nordestgaard, BG; Sillesen, H; Tybjaerg-Hansen, A, 2009)
" We found a consistent and highly significant gene-nutrient interaction showing a strong dose-response effect."1.31Dietary fat intake determines the effect of a common polymorphism in the hepatic lipase gene promoter on high-density lipoprotein metabolism: evidence of a strong dose effect in this gene-nutrient interaction in the Framingham Study. ( Coltell, O; Corella, D; Couture, P; Cupples, LA; Demissie, S; Ordovas, JM; Schaefer, EJ; Tucker, KL; Wilson, PW, 2002)

Research

Studies (67)

TimeframeStudies, this research(%)All Research%
pre-19908 (11.94)18.7374
1990's6 (8.96)18.2507
2000's23 (34.33)29.6817
2010's20 (29.85)24.3611
2020's10 (14.93)2.80

Authors

AuthorsStudies
Xia, M1
Ma, S1
Huang, Q1
Zeng, H1
Ge, J1
Xu, W1
Wu, Q1
Wu, L1
Li, X1
Ma, H1
Chen, L1
Li, Q1
Aleteng, Q1
Hu, Y1
He, W1
Pan, B1
Lin, H1
Zheng, Y1
Wang, S1
Tang, H1
Gao, X1
Fraga, LN1
Milenkovic, D1
Coutinho, CP1
Rozenbaum, AC1
Lajolo, FM1
Hassimotto, NMA1
Silbernagel, G1
Chen, YQ1
Rief, M1
Kleber, ME2
Hoffmann, MM1
Stojakovic, T1
Stang, A1
Sarzynski, MA1
Bouchard, C2
März, W2
Qian, YW1
Scharnagl, H1
Konrad, RJ1
Meng, W1
Adam, LP1
Behnia, K1
Zhao, L1
Yang, R1
Kopcho, LM1
Locke, GA1
Taylor, DS1
Yin, X1
Wexler, RR1
Finlay, H1
Brouwers, MCGJ1
Simons, N1
Stehouwer, CDA1
Isaacs, A1
Wijarnpreecha, K1
Scribani, M1
Raymond, P1
Harnois, DM1
Keaveny, AP1
Ahmed, A1
Kim, D1
Hara, Y3
Zhang, B3
Suzuki, A3
Yamaguchi, S3
Adachi, J1
Tomonaga, T1
Yasunaga, S1
Saku, K1
Aoyama, T2
Hirano, KI3
Lombardi, R1
Iuculano, F1
Pallini, G1
Fargion, S1
Fracanzani, AL1
Dongiovanni, P1
Paolini, E1
Corsini, A1
Sirtori, CR1
Ruscica, M1
Nagayama, D1
Saiki, A1
Watanabe, Y1
Yamaguchi, T1
Ohira, M1
Sato, N1
Kanayama, M1
Moroi, M1
Miyashita, Y1
Shirai, K1
Tatsuno, I1
Salazar-Tortosa, DF1
Pascual-Gamarra, JM1
Labayen, I1
Rupérez, AI1
Censi, L1
Béghin, L1
Michels, N1
González-Gross, M1
Manios, Y1
Lambrinou, CP1
Moreno, LA1
Meirhaeghe, A1
Castillo, MJ1
Ruiz, JR1
Steinberg, WM1
Buse, JB1
Ghorbani, MLM1
Ørsted, DD1
Nauck, MA1
Carter, D1
Dieterich, DT1
Chang, C1
Li, M2
Miyauchi, H2
Ikeda, Y4
Higashi, M2
Takagi, A2
Nagasaka, H2
Kobayashi, K3
Magata, Y1
Stefan, N2
Häring, HU2
Cusi, K1
Rhainds, D1
Tardif, JC1
Hashimoto, C1
Kozawa, J1
Sugimura, K1
Futsukaichi, Y1
Zaima, N1
Shrestha, R1
Nakamura, H1
Kawaguchi, K1
Sai, E1
Hui, SP1
Nakano, Y1
Sawamura, A1
Inaba, T1
Sakata, Y1
Yasui, Y1
Nagasawa, Y1
Kinugawa, S1
Shimada, K1
Yamada, S1
Hao, H1
Nakatani, D1
Ide, T1
Amano, T1
Naito, H1
Pongprasobchai, S1
Elshourbagy, NA1
Meyers, HV1
Abdel-Meguid, SS1
Del Ben, M1
Polimeni, L1
Brancorsini, M1
Di Costanzo, A1
D'Erasmo, L1
Baratta, F1
Loffredo, L1
Pastori, D1
Pignatelli, P1
Violi, F1
Arca, M1
Angelico, F1
Posadas-Sánchez, R1
Ocampo-Arcos, WA1
López-Uribe, ÁR1
Posadas-Romero, C1
Villarreal-Molina, T1
León, EÁ1
Pérez-Hernández, N1
Rodríguez-Pérez, JM1
Cardoso-Saldaña, G1
Medina-Urrutia, A1
Vargas-Alarcón, G1
Suomela, E1
Oikonen, M1
Pitkänen, N1
Ahola-Olli, A1
Virtanen, J1
Parkkola, R1
Jokinen, E1
Laitinen, T1
Hutri-Kähönen, N1
Kähönen, M1
Lehtimäki, T1
Taittonen, L1
Tossavainen, P1
Jula, A1
Loo, BM1
Mikkilä, V1
Telama, R1
Viikari, JSA1
Juonala, M1
Raitakari, OT1
Xu, L1
Jiang, CQ1
Lam, TH1
Zhang, WS1
Zhu, F1
Jin, YL1
Thomas, GN1
Cheng, KK1
Schooling, CM1
Goodman, KB1
Bury, MJ1
Cheung, M1
Cichy-Knight, MA1
Dowdell, SE1
Dunn, AK1
Lee, D1
Lieby, JA1
Moore, ML1
Scherzer, DA1
Sha, D1
Suarez, DP1
Murphy, DJ1
Harpel, MR1
Manas, ES1
McNulty, DE1
Annan, RS1
Matico, RE1
Schwartz, BK1
Trill, JJ1
Sweitzer, TD1
Wang, DY1
Keller, PM1
Krawiec, JA1
Jaye, MC1
Johannsen, TH1
Kamstrup, PR1
Andersen, RV1
Jensen, GB1
Sillesen, H1
Tybjaerg-Hansen, A1
Nordestgaard, BG1
Fazio, S1
Linton, MF1
Mitchell, GA1
Muntoni, S2
Atzori, L1
Mereu, R1
Manca, A1
Satta, G1
Gentilini, A1
Bianco, P1
Baule, A1
Baule, GM1
Rosenson, RS1
Johansen, CT1
Gallinger, ZR1
Wang, J1
Ban, MR1
Young, TK1
Bjerregaard, P1
Hegele, RA1
Grammer, TB1
Castanho, VS1
Gidlund, M1
Nakamura, R1
de Faria, EC2
Miksztowicz, V1
Lucero, D1
Zago, V1
Cacciagiú, L1
Lopez, G1
Gonzalez Ballerga, E1
Sordá, J1
Fassio, E1
Schreier, L1
Berg, G1
Ampuero, J1
Romero-Gómez, M1
Han, Z1
Heath, SC1
Shmulewitz, D1
Li, W1
Auerbach, SB1
Blundell, ML1
Lehner, T1
Ott, J1
Stoffel, M1
Friedman, JM1
Breslow, JL1
Ordovas, JM3
Corella, D2
Demissie, S1
Cupples, LA1
Couture, P1
Coltell, O1
Wilson, PW1
Schaefer, EJ1
Tucker, KL1
Zambon, A1
Deeb, SS1
Pauletto, P1
Crepaldi, G1
Brunzell, JD1
Alarcon, SB1
Oliveira, HC1
Harada, LM1
Nunes, VS1
Kaplan, D1
Quintão, EC1
Rader, DJ1
GOTTSEGEN, G1
TOROK, E1
Poston, WS1
Reeves, RS1
Haddock, CK1
Stormer, S1
Balasubramanyam, A1
Satterwhite, O1
Taylor, JE1
Foreyt, JP2
Didangelos, TP1
Thanopoulou, AK1
Bousboulas, SH1
Sambanis, CL1
Athyros, VG1
Spanou, EA1
Dimitriou, KC1
Pappas, SI1
Karamanos, BG1
Karamitsos, DT1
Hutter, CM1
Austin, MA2
Farin, FM1
Viernes, HM1
Edwards, KL2
Leonetti, DL1
McNeely, MJ1
Fujimoto, WY1
Nelson, RH1
Miles, JM1
Miljkovic-Gacic, I1
Bunker, CH1
Ferrell, RE1
Kammerer, CM1
Evans, RW1
Patrick, AL1
Kuller, LH1
Paradis, ME1
Lamarche, B1
Annuzzi, G1
Santo, AS1
Cunningham, AM1
Alhassan, S1
Browne, RW1
Burton, H1
Leddy, JJ1
Grandjean, PW1
Horvath, SM1
Horvath, PJ1
Lacour, B1
Roullet, JB1
Drueke, T1
Pérusse, L1
Rice, T1
Després, JP1
Bergeron, J1
Province, MA1
Gagnon, J1
Leon, AS1
Rao, DC1
Skinner, JS1
Wilmore, JH1
Zavoral, JH2
Davidson, MH1
Hauptman, J3
DiGirolamo, M1
Halsted, CH1
Heber, D1
Heimburger, DC1
Lucas, CP1
Robbins, DC1
Chung, J1
Heymsfield, SB1
Uusitupa, M1
Hill, JO1
Anderson, JW1
Fujioka, K1
O'Neil, PM1
Smith, DK1
Aronne, LJ1
Lucas, C1
Boldrin, MN1
Collins, H1
Segal, KR1
Friedlander, Y1
Talmud, PJ1
Humphries, SE1
Cohn, G1
Valdes, G1
Capuzzi , DM1
Shen, H1
Alexander, JP1
Barron, DW1
Blomhoff, JP1
Hayakawa, T1
Kondo, T1
Shibata, T1
Kitagawa, M1
Ono, H1
Sakai, Y1
Kiriyama, S1
Haffner, SM1
Fong, D1
Hazuda, HP1
Pugh, JA1
Patterson, JK1
Crona, N1
Enk, L1
Mattsson, LA1
Samsioe, G1
Silfverstolpe, G1
Williams, PT1
Krauss, RM1
Wood, PD1
Lindgren, FT1
Giotas, C1
Vranizan, KM1
Förster, W1

Clinical Trials (6)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Long-term, Multi-centre, International, Randomised Double-blind, Placebo-controlled Trial to Determine Liraglutide Effects on Cardiovascular Events[NCT01179048]Phase 39,341 participants (Actual)Interventional2010-08-31Completed
The Role of Microbiome Reprogramming on Liver Fat Accumulation[NCT03914495]57 participants (Actual)Interventional2019-05-21Terminated (stopped due to PI carefully considered multiple factors and decided to close study to any further enrollment.)
Comparative Clinical Study to Evaluate the Possible Beneficial Effect of Empagliflozin Versus Pioglitazone on Non-diabetic Patients With Non-Alcoholic Steatohepatitis[NCT05605158]Phase 356 participants (Anticipated)Interventional2022-11-30Not yet recruiting
A Randomised Controlled International Multicentre Study Evaluating Changes in Metabolic Syndrome in Smokers With Type 2 Diabetes Mellitus After Switching From Tobacco Cigarettes to Combustion-Free Nicotine Delivery Systems: DIASMOKE Study[NCT04231838]576 participants (Anticipated)Interventional2021-09-27Recruiting
Health, Risk Factors, Exercise Training, and Genetics[NCT00005137]0 participants Interventional1992-07-31Completed
Diabetes and Cardiovascular Risk In Mexico City (San Antonio Heart Study)[NCT00005146]0 participants Observational1979-05-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Time From Rand. to First Occurrence of an Expanded Composite Cardiovascular Outcome Defined as Either Cardiovascular Death, Non-fatal Myocardial Infarction, Non-fatal Stroke, Revascularisation, Hospitalisation for Unstable Angina or for Heart Failure.

Time from randomisation to first occurrence of an expanded composite cardiovascular outcome defined as either cardiovascular death, non-fatal myocardial infarction, non-fatal stroke, coronary revascularisation, hospitalisation for unstable angina or for heart failure. The percentage of subjects experiencing first occurrence of an expanded composite cardiovascular outcome defined as either cardiovascular death, non-fatal myocardial infarction, non-fatal stroke, coronary revascularisation, hospitalisation for unstable angina or for heart failure is presented. (NCT01179048)
Timeframe: from randomisation (visit 3; month 0) to last contact (visit 16; up to month 60+30 days)

Interventionpercentage of subjects (Number)
Liraglutide20.3
Placebo22.7

Time From Randomisation to All Cause Death

Time from randomisation to all cause death. The percentage of subjects with a death by any cause (all-cause death) is presented. (NCT01179048)
Timeframe: from randomisation (visit 3; month 0) to last contact (visit 16; up to month 60+30 days)

Interventionpercentage of subjects (Number)
Liraglutide8.2
Placebo9.6

Time From Randomisation to First Occurrence of a Composite Microvascular Outcome

"Time from randomisation to first occurrence of a composite microvascular outcome, defined as any one of the following:~new onset of persistent macroalbuminuria~persistent doubling of serum creatinine~need for continuous renal replacement therapy~death due to renal disease~need for retinal photocoagulation or treatment with intravitreal agents~vitreous haemorrhage~diabetes-related blindness~The percentage of subjects experiencing a first occurrence of a composite microvascular outcome is presented." (NCT01179048)
Timeframe: from randomisation (visit 3; month 0) to last contact (visit 16; up to month 60+30 days)

InterventionPercentage of subjects (Number)
Liraglutide7.6
Placebo8.9

Time From Randomisation to First Occurrence of Cardiovascular Death, Non-fatal Myocardial Infarction, or Non-fatal Stroke (a Composite Cardiovascular Outcome)

Time from randomisation to first occurrence of cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke (a composite cardiovascular outcome). The percentage of subjects experiencing a first event of cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke (a composite cardiovascular outcome) is presented. (NCT01179048)
Timeframe: from randomisation (visit 3; month 0) to last contact (visit 16; up to month 60+30 days)

Interventionpercentage of subjects (Number)
Liraglutide13.0
Placebo14.9

Time From Randomisation to Each Individual Component of the Composite Microvascular Outcome and to the Retinopathy and Nephropathy Composite Outcomes Separately.

Time from randomisation to each individual component of the composite microvascular outcome and to the retinopathy and nephropathy composite outcomes separately. The percentage of subjects experiencing each individual component of the composite microvascular outcome are presented. (NCT01179048)
Timeframe: from randomisation (visit 3; month 0) to last contact (visit 16; up to month 60+30 days)

,
InterventionPercentage of subjects (Number)
Nephropathy compositeNew onset of persistent macroalbuminuriaPersistent doubling of serum creatinineNeed for continuous renal-replacement therapyDeath due to renal diseaseRetinopathy compositeTreatment with photocoagulation/intravitreal agentDevelopment of diabetes-related blindnessVitreous haemorrhage
Liraglutide5.73.41.91.20.22.32.10.00.7
Placebo7.24.62.11.40.12.01.80.020.5

Time From Randomisation to Each Individual Component of the Expanded Composite Cardiovascular Outcome

Time from randomisation to each individual component of the expanded composite cardiovascular outcome. The percentage of subjects experiencing each of the individual component of the expanded composite cardiovascular outcome (defined as either cardiovascular death, non-fatal myocardial infarction, non-fatal stroke, coronary revascularisation, hospitalisation for unstable angina or heart failure) is presented. (NCT01179048)
Timeframe: from randomisation (visit 3; month 0) to last contact (visit 16; up to month 60+30 days)

,
Interventionpercentage of subjects (Number)
Cardiovascular deathNon-fatal strokeNon-fatal myocardial infarctionUnstable angina pectoris (hospitalisation)Coronary revascularisationHeart failure (hospitalisation)
Liraglutide4.73.46.02.68.74.7
Placebo6.03.86.82.79.45.3

Reviews

23 reviews available for 1-anilino-8-naphthalenesulfonate and Cardiovascular Diseases

ArticleYear
Non-alcoholic fatty liver disease and cardiovascular disease: assessing the evidence for causality.
    Diabetologia, 2020, Volume: 63, Issue:2

    Topics: Animals; Cardiovascular Diseases; Humans; Lipase; Membrane Proteins; Non-alcoholic Fatty Liver Disea

2020
Nutrients, Genetic Factors, and Their Interaction in Non-Alcoholic Fatty Liver Disease and Cardiovascular Disease.
    International journal of molecular sciences, 2020, Nov-19, Volume: 21, Issue:22

    Topics: Apolipoproteins; Cardiovascular Diseases; Diet; Epigenesis, Genetic; Fatty Acids, Unsaturated; Fruct

2020
Nonalcoholic fatty liver disease or metabolic dysfunction-associated fatty liver disease diagnoses and cardiovascular diseases: From epidemiology to drug approaches.
    European journal of clinical investigation, 2021, Volume: 51, Issue:7

    Topics: Acyltransferases; Cardiovascular Diseases; Coronary Artery Disease; Diabetes Mellitus, Type 2; Dysli

2021
Nonalcoholic Fatty Liver Disease/Nonalcoholic Steatohepatitis in Liver Transplantation.
    Clinics in liver disease, 2018, Volume: 22, Issue:1

    Topics: Cardiovascular Diseases; Diabetes Complications; Humans; Kidney Diseases; Lipase; Liver Transplantat

2018
Non-alcoholic fatty liver disease: causes, diagnosis, cardiometabolic consequences, and treatment strategies.
    The lancet. Diabetes & endocrinology, 2019, Volume: 7, Issue:4

    Topics: Antioxidants; Bariatric Surgery; Carcinoma, Hepatocellular; Cardiovascular Diseases; Diabetes Mellit

2019
Non-alcoholic fatty liver disease: causes, diagnosis, cardiometabolic consequences, and treatment strategies.
    The lancet. Diabetes & endocrinology, 2019, Volume: 7, Issue:4

    Topics: Antioxidants; Bariatric Surgery; Carcinoma, Hepatocellular; Cardiovascular Diseases; Diabetes Mellit

2019
Non-alcoholic fatty liver disease: causes, diagnosis, cardiometabolic consequences, and treatment strategies.
    The lancet. Diabetes & endocrinology, 2019, Volume: 7, Issue:4

    Topics: Antioxidants; Bariatric Surgery; Carcinoma, Hepatocellular; Cardiovascular Diseases; Diabetes Mellit

2019
Non-alcoholic fatty liver disease: causes, diagnosis, cardiometabolic consequences, and treatment strategies.
    The lancet. Diabetes & endocrinology, 2019, Volume: 7, Issue:4

    Topics: Antioxidants; Bariatric Surgery; Carcinoma, Hepatocellular; Cardiovascular Diseases; Diabetes Mellit

2019
From HDL-cholesterol to HDL-function: cholesterol efflux capacity determinants.
    Current opinion in lipidology, 2019, Volume: 30, Issue:2

    Topics: Antigens, Nuclear; Apolipoprotein A-I; Apolipoproteins E; Biological Assay; Biological Transport; Bi

2019
Maldigestion from pancreatic exocrine insufficiency.
    Journal of gastroenterology and hepatology, 2013, Volume: 28 Suppl 4

    Topics: Administration, Oral; Atherosclerosis; Breath Tests; Cardiovascular Diseases; Diet, Fat-Restricted;

2013
Cholesterol: the good, the bad, and the ugly - therapeutic targets for the treatment of dyslipidemia.
    Medical principles and practice : international journal of the Kuwait University, Health Science Centre, 2014, Volume: 23, Issue:2

    Topics: Animals; Apolipoprotein A-I; Apolipoproteins B; Atherosclerosis; Cardiovascular Diseases; Cholestero

2014
Genetics, physiology and perinatal influences in childhood obesity: view from the Chair.
    International journal of obesity (2005), 2009, Volume: 33 Suppl 1

    Topics: Adipocytes; Adipose Tissue; Adult; Age of Onset; Cardiovascular Diseases; Child; Fatty Acids; Female

2009
[High-density lipoprotein (HDL) and cholesteryl ester transfer protein (CETP): role in lipid metabolism and clinical meaning].
    MMW Fortschritte der Medizin, 2010, Jul-01, Volume: 152 Suppl 2

    Topics: Anticholesteremic Agents; Apolipoprotein A-I; Cardiovascular Diseases; Cholesterol Ester Transfer Pr

2010
[Influence of non-alcoholic fatty liver disease on cardiovascular disease].
    Gastroenterologia y hepatologia, 2012, Volume: 35, Issue:8

    Topics: Apolipoprotein C-III; Atherosclerosis; Cardiovascular Diseases; Carotid Intima-Media Thickness; Chol

2012
Hepatic lipase: a marker for cardiovascular disease risk and response to therapy.
    Current opinion in lipidology, 2003, Volume: 14, Issue:2

    Topics: Animals; Cardiovascular Diseases; Genetic Predisposition to Disease; Humans; Lipase; Liver; Polymorp

2003
Regulation of reverse cholesterol transport and clinical implications.
    The American journal of cardiology, 2003, Aug-18, Volume: 92, Issue:4A

    Topics: Animals; Apolipoprotein A-I; ATP Binding Cassette Transporter 1; ATP-Binding Cassette Transporters;

2003
Genes, diet and plasma lipids: the evidence from observational studies.
    World review of nutrition and dietetics, 2004, Volume: 93

    Topics: Apolipoproteins; Cardiovascular Diseases; Diet; Gene Frequency; Genetic Predisposition to Disease; G

2004
The use of orlistat in the treatment of obesity, dyslipidaemia and Type 2 diabetes.
    Expert opinion on pharmacotherapy, 2005, Volume: 6, Issue:14

    Topics: Anti-Obesity Agents; Cardiovascular Diseases; Diabetes Mellitus, Type 2; Diet, Fat-Restricted; Dysli

2005
Endothelial lipase: its role in cardiovascular disease.
    The Canadian journal of cardiology, 2006, Volume: 22 Suppl B

    Topics: Animals; Apolipoproteins; Cardiovascular Diseases; Cholesterol, HDL; Humans; Lipase; Lipid Metabolis

2006
[Lipid metabolism disorders in chronic kidney failure].
    Nephrologie, 1983, Volume: 4, Issue:2

    Topics: Apoproteins; Cardiovascular Diseases; Hormones; Humans; Kidney Failure, Chronic; Lipase; Lipids; Lip

1983
New aspects in the management of obesity: operation and the impact of lipase inhibitors.
    Current opinion in lipidology, 1999, Volume: 10, Issue:1

    Topics: Cardiovascular Diseases; Diabetes Mellitus, Type 2; Enzyme Inhibitors; Humans; Lactones; Lipase; Mul

1999
Pathophysiology and treatment of the dyslipidemia of insulin resistance.
    Current cardiology reports, 2001, Volume: 3, Issue:5

    Topics: Cardiovascular Diseases; Enzyme Inhibitors; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors;

2001
Pharmacogenetics of Lipid-lowering Therapies.
    Current atherosclerosis reports, 2002, Volume: 4, Issue:3

    Topics: Apolipoproteins E; Aryldialkylphosphatase; ATP Binding Cassette Transporter 1; ATP-Binding Cassette

2002
Lipoproteins, lipases, and the metabolic cardiovascular syndrome.
    Journal of cardiovascular pharmacology, 1992, Volume: 20 Suppl 8

    Topics: Blood Glucose; Cardiovascular Diseases; Coronary Disease; Down-Regulation; Eating; Fatty Acids, None

1992
Progestogens and lipid metabolism.
    Maturitas, 1986, Volume: 8, Issue:2

    Topics: Adipose Tissue; Animals; Cardiovascular Diseases; Chemical Phenomena; Chemistry; Drug Combinations;

1986
[Prostaglandins and cardiovascular diseases].
    Das Deutsche Gesundheitswesen, 1972, Nov-30, Volume: 27, Issue:48

    Topics: Adolescent; Animals; Animals, Laboratory; Arteriosclerosis; Blood Coagulation Disorders; Cardiovascu

1972

Trials

9 trials available for 1-anilino-8-naphthalenesulfonate and Cardiovascular Diseases

ArticleYear
Prevention of Cardiovascular Events with Pitavastatin is Associated with Increased Serum Lipoprotein Lipase Mass Level: Subgroup Analysis of the TOHO-LIP.
    Journal of atherosclerosis and thrombosis, 2022, Apr-01, Volume: 29, Issue:4

    Topics: Cardiovascular Diseases; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Lipase; Lipoprotein

2022
Amylase, Lipase, and Acute Pancreatitis in People With Type 2 Diabetes Treated With Liraglutide: Results From the LEADER Randomized Trial.
    Diabetes care, 2017, Volume: 40, Issue:7

    Topics: Acute Disease; Amylases; Cardiovascular Diseases; Diabetes Mellitus, Type 2; Double-Blind Method; Fe

2017
Weight loss in obese Mexican Americans treated for 1-year with orlistat and lifestyle modification.
    International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity, 2003, Volume: 27, Issue:12

    Topics: Adult; Aged; Anti-Obesity Agents; Behavior Therapy; Cardiovascular Diseases; Combined Modality Thera

2003
The ORLIstat and CArdiovascular risk profile in patients with metabolic syndrome and type 2 DIAbetes (ORLICARDIA) Study.
    Current medical research and opinion, 2004, Volume: 20, Issue:9

    Topics: Anti-Obesity Agents; Blood Glucose; Cardiovascular Diseases; Diabetes Mellitus, Type 2; Diet, Reduci

2004
NMR analysis of lipoprotein particle size does not increase sensitivity to the effect of soy protein on CVD risk when compared with the traditional lipid profile.
    Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme, 2008, Volume: 33, Issue:3

    Topics: Adolescent; Adult; Apolipoproteins; Blood Glucose; Cardiovascular Diseases; Cholesterol; Cholesterol

2008
Treatment with orlistat reduces cardiovascular risk in obese patients.
    Journal of hypertension, 1998, Volume: 16, Issue:12 Pt 2

    Topics: Adult; Aged; Blood Glucose; Blood Pressure; Cardiovascular Diseases; Diet, Reducing; Double-Blind Me

1998
Weight control and risk factor reduction in obese subjects treated for 2 years with orlistat: a randomized controlled trial.
    JAMA, 1999, Jan-20, Volume: 281, Issue:3

    Topics: Adult; Analysis of Variance; Blood Glucose; Blood Pressure; Cardiovascular Diseases; Double-Blind Me

1999
Orlistat, a lipase inhibitor, for weight maintenance after conventional dieting: a 1-y study.
    The American journal of clinical nutrition, 1999, Volume: 69, Issue:6

    Topics: Adult; Anti-Obesity Agents; Behavior Therapy; Cardiovascular Diseases; Cholesterol, HDL; Dietary Fat

1999
Orlistat in the long-term treatment of obesity in primary care settings.
    Archives of family medicine, 2000, Volume: 9, Issue:2

    Topics: Adult; Anti-Obesity Agents; Blood Glucose; Blood Pressure; Cardiovascular Diseases; Double-Blind Met

2000

Other Studies

35 other studies available for 1-anilino-8-naphthalenesulfonate and Cardiovascular Diseases

ArticleYear
NAFLD-related gene polymorphisms and all-cause and cause-specific mortality in an Asian population: the Shanghai Changfeng Study.
    Alimentary pharmacology & therapeutics, 2022, Volume: 55, Issue:6

    Topics: Adult; Cardiovascular Diseases; Cause of Death; China; Genetic Predisposition to Disease; Genome-Wid

2022
Interaction between APOE, APOA1, and LPL Gene Polymorphisms and Variability in Changes in Lipid and Blood Pressure following Orange Juice Intake: A Pilot Study.
    Molecular nutrition & food research, 2023, Volume: 67, Issue:13

    Topics: Apolipoprotein A-I; Apolipoproteins E; Blood Pressure; Cardiovascular Diseases; Citrus sinensis; Fla

2023
Inverse association between apolipoprotein C-II and cardiovascular mortality: role of lipoprotein lipase activity modulation.
    European heart journal, 2023, Jul-01, Volume: 44, Issue:25

    Topics: Apolipoprotein C-II; Apolipoprotein C-III; Cardiovascular Diseases; Humans; Lipase; Lipoprotein Lipa

2023
Benzothiazole-based compounds as potent endothelial lipase inhibitors.
    Bioorganic & medicinal chemistry letters, 2019, 10-15, Volume: 29, Issue:20

    Topics: Animals; Benzothiazoles; Cardiovascular Diseases; Drug Evaluation, Preclinical; Enzyme Inhibitors; G

2019
PNPLA3 gene polymorphism and overall and cardiovascular mortality in the United States.
    Journal of gastroenterology and hepatology, 2020, Volume: 35, Issue:10

    Topics: Adult; Alleles; Cardiovascular Diseases; Comorbidity; Female; Follow-Up Studies; Genetic Association

2020
Effect of Tricaprin on Cardiac Proteome in a Mouse Model for Triglyceride Deposit Cardiomyovasculopathy.
    Journal of oleo science, 2020, Nov-25, Volume: 69, Issue:12

    Topics: Animals; Cardiovascular Diseases; Dietary Supplements; Disease Models, Animal; Female; Lipase; Lipol

2020
Interplay of physical activity and genetic variants of the endothelial lipase on cardiovascular disease risk factors.
    Pediatric research, 2022, Volume: 91, Issue:4

    Topics: Adolescent; Cardiovascular Diseases; Exercise; Heart Disease Risk Factors; Humans; Lipase; Lipids; R

2022
Tricaprin Rescues Myocardial Abnormality in a Mouse Model of Triglyceride Deposit Cardiomyovasculopathy.
    Journal of oleo science, 2018, Aug-01, Volume: 67, Issue:8

    Topics: Animals; Cardiovascular Diseases; Disease Models, Animal; Fatty Acids; Heart; Humans; Lipase; Mice,

2018
Triglyceride deposit cardiomyovasculopathy: a rare cardiovascular disorder.
    Orphanet journal of rare diseases, 2019, 06-11, Volume: 14, Issue:1

    Topics: Adult; Aged; Atherosclerosis; Cardiovascular Diseases; Female; Humans; Lipase; Male; Middle Aged; Mu

2019
Non-alcoholic fatty liver disease, metabolic syndrome and patatin-like phospholipase domain-containing protein3 gene variants.
    European journal of internal medicine, 2014, Volume: 25, Issue:6

    Topics: Adult; Aged; Cardiovascular Diseases; Cohort Studies; Female; Genetic Predisposition to Disease; Hum

2014
Hepatic lipase (LIPC) C-514T gene polymorphism is associated with cardiometabolic parameters and cardiovascular risk factors but not with fatty liver in Mexican population.
    Experimental and molecular pathology, 2015, Volume: 98, Issue:1

    Topics: Adult; Aged; Apolipoprotein A-I; Biomarkers; Cardiovascular Diseases; Case-Control Studies; Choleste

2015
Childhood predictors of adult fatty liver. The Cardiovascular Risk in Young Finns Study.
    Journal of hepatology, 2016, Volume: 65, Issue:4

    Topics: Adolescent; Cardiovascular Diseases; Child; Fatty Liver; Finland; Genetic Predisposition to Disease;

2016
Mendelian randomization estimates of alanine aminotransferase with cardiovascular disease: Guangzhou Biobank Cohort study.
    Human molecular genetics, 2017, 01-15, Volume: 26, Issue:2

    Topics: Alanine Transaminase; Biological Specimen Banks; Cardiovascular Diseases; Cohort Studies; Female; Ge

2017
Discovery of potent, selective sulfonylfuran urea endothelial lipase inhibitors.
    Bioorganic & medicinal chemistry letters, 2009, Jan-01, Volume: 19, Issue:1

    Topics: Animals; Cardiovascular Diseases; Drug Discovery; Drug Evaluation, Preclinical; Endothelium; Enzyme

2009
Hepatic lipase, genetically elevated high-density lipoprotein, and risk of ischemic cardiovascular disease.
    The Journal of clinical endocrinology and metabolism, 2009, Volume: 94, Issue:4

    Topics: Adult; Amino Acid Substitution; Cardiovascular Diseases; Cerebral Hemorrhage; Cholesterol, HDL; Denm

2009
Elevated high-density lipoprotein (HDL) levels due to hepatic lipase mutations do not reduce cardiovascular disease risk: another strike against the HDL dogma.
    The Journal of clinical endocrinology and metabolism, 2009, Volume: 94, Issue:4

    Topics: Cardiovascular Diseases; Carrier State; Cholesterol, HDL; Genetic Variation; Humans; Lipase; Lipopro

2009
Risk factors for cardiovascular disease in Sardinia from 1978 to 2001: a comparative study with Italian mainland.
    European journal of internal medicine, 2009, Volume: 20, Issue:4

    Topics: Adult; Age Distribution; Aged; Aged, 80 and over; Apolipoproteins A; Blood Glucose; Cardiovascular D

2009
Functional assessment of HDL: Moving beyond static measures for risk assessment.
    Cardiovascular drugs and therapy, 2010, Volume: 24, Issue:1

    Topics: Amides; Animals; Anticholesteremic Agents; Azetidines; Cardiovascular Diseases; Cholesterol; Cholest

2010
Rare ATGL haplotypes are associated with increased plasma triglyceride concentrations in the Greenland Inuit.
    International journal of circumpolar health, 2010, Volume: 69, Issue:1

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Cardiovascular Diseases; Female; Genotype; Greenland; Ha

2010
The metabolically benign and malignant fatty liver.
    Diabetes, 2011, Volume: 60, Issue:8

    Topics: Animals; Cardiovascular Diseases; Child; Diabetes Mellitus, Type 1; Fatty Liver; Hepatitis; Humans;

2011
Post-menopausal hormone therapy reduces autoantibodies to oxidized apolipoprotein B100.
    Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, 2011, Volume: 27, Issue:10

    Topics: Adult; Aged; Aged, 80 and over; Apolipoprotein B-100; Autoantibodies; Autoimmune Diseases; Cardiovas

2011
Hepatic lipase activity is increased in non-alcoholic fatty liver disease beyond insulin resistance.
    Diabetes/metabolism research and reviews, 2012, Volume: 28, Issue:6

    Topics: Atherosclerosis; Cardiovascular Diseases; Fatty Liver; Humans; Insulin Resistance; Lipase; Liver; No

2012
Candidate genes involved in cardiovascular risk factors by a family-based association study on the island of Kosrae, Federated States of Micronesia.
    American journal of medical genetics, 2002, Jul-01, Volume: 110, Issue:3

    Topics: Adult; Aged; Aged, 80 and over; Alleles; Apolipoprotein A-I; Apolipoprotein A-II; Apolipoproteins E;

2002
Dietary fat intake determines the effect of a common polymorphism in the hepatic lipase gene promoter on high-density lipoprotein metabolism: evidence of a strong dose effect in this gene-nutrient interaction in the Framingham Study.
    Circulation, 2002, Oct-29, Volume: 106, Issue:18

    Topics: Adult; Aged; Alleles; Cardiovascular Diseases; Cholesterol, HDL; Cohort Studies; Demography; Dietary

2002
Moderate hyperalphalipoproteinaemia in a Brazilian population is related to lipoprotein lipase activity, apolipoprotein A-I concentration, age and body mass index.
    Clinical science (London, England : 1979), 2004, Volume: 106, Issue:1

    Topics: Adult; Age Factors; Aged; Apolipoprotein A-I; Body Mass Index; Cardiovascular Diseases; Carrier Prot

2004
[Studies on the treatment of circulatory diseases. II. Administration of vasolastine in coronary sclerosis].
    Orvosi hetilap, 1960, Oct-30, Volume: 101

    Topics: Cardiovascular Diseases; Coronary Artery Disease; Coronary Disease; Enzyme Therapy; Enzymes; Humans;

1960
Association of endothelial lipase gene (LIPG) haplotypes with high-density lipoprotein cholesterol subfractions and apolipoprotein AI plasma levels in Japanese Americans.
    Atherosclerosis, 2006, Volume: 185, Issue:1

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Apolipoprotein A-I; Asian; Cardiovascular Disea

2006
Lipoprotein subclass and particle size differences in Afro-Caribbeans, African Americans, and white Americans: associations with hepatic lipase gene variation.
    Metabolism: clinical and experimental, 2006, Volume: 55, Issue:1

    Topics: Adult; Age Factors; Aged; Alleles; Black or African American; Body Mass Index; Cardiovascular Diseas

2006
Genetic and environmental modulation of postprandial lipemia: from a better knowledge of the mechanisms to a more effective treatment strategy.
    Nutrition, metabolism, and cardiovascular diseases : NMCD, 2008, Volume: 18, Issue:3

    Topics: Cardiovascular Diseases; Environment; Genetic Predisposition to Disease; Humans; Hyperlipidemias; Li

2008
Familial resemblance of plasma lipids, lipoproteins and postheparin lipoprotein and hepatic lipases in the HERITAGE Family Study.
    Arteriosclerosis, thrombosis, and vascular biology, 1997, Volume: 17, Issue:11

    Topics: Adolescent; Cardiovascular Diseases; Cohort Studies; Diabetes Mellitus; Enzyme Induction; Exercise;

1997
Sib-pair linkage analysis of longitudinal changes in lipoprotein risk factors and lipase genes in women twins.
    Journal of lipid research, 2000, Volume: 41, Issue:8

    Topics: Adult; Cardiovascular Diseases; Female; Genetic Linkage; Genetic Predisposition to Disease; Humans;

2000
Biochemical disturbances associated with total hip replacement.
    The Journal of bone and joint surgery. British volume, 1979, Volume: 61, Issue:1

    Topics: Arrhythmias, Cardiac; Arthroplasty; Bone Cements; Cardiovascular Diseases; Hip Joint; Humans; Hypote

1979
Enzyme immunoassay for serum pancreatic lipase in the diagnosis of pancreatic diseases.
    Gastroenterologia Japonica, 1989, Volume: 24, Issue:5

    Topics: Adult; Amylases; Cardiovascular Diseases; Digestive System Diseases; Female; Humans; Immunoenzyme Te

1989
Hyperinsulinemia, upper body adiposity, and cardiovascular risk factors in non-diabetics.
    Metabolism: clinical and experimental, 1988, Volume: 37, Issue:4

    Topics: Adipose Tissue; Adult; Blood Pressure; Cardiovascular Diseases; Cholesterol, HDL; Female; Hispanic o

1988
Lipoprotein subfractions of runners and sedentary men.
    Metabolism: clinical and experimental, 1986, Volume: 35, Issue:1

    Topics: Adipose Tissue; Adult; Body Weight; Cardiovascular Diseases; Female; Humans; Lipase; Lipoprotein Lip

1986