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Jmp version 12.2 for windows

Manufactured by SAS Institute
Sourced in United States

JMP version 12.2 for Windows is a statistical discovery software that provides tools for data analysis, visualization, and modeling. It allows users to explore data, fit statistical models, and generate reports. The software is designed to run on the Windows operating system.

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Lab products found in correlation

2 protocols using jmp version 12.2 for windows

1

Cardiovascular Remodeling Risk Factors

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Continuous variables are expressed as means ± standard deviation or medians (interquartile range; IQR) depending on their distribution. Categorical variables are expressed as percentages. Continuous variables were compared using Student’s t-test or the Wilcoxon rank-sum test. Categorical variables were compared using the chi-squared test. Propensity scores were calculated, using age, sex, body mass index (BMI), and the presence of diabetes mellitus, dyslipidaemia, and hypertension as covariates. Patients in the two groups were matched through the greedy matching protocol with a fixed calliper width of 0.20.
Logistic regression analyses were used to estimate the relative risk of CAE and of excessive expansive CA remodelling, respectively. Model 1 was adjusted for variables showing values of p < 0.05 on univariate analyses (CAE: AAA and BMI, Excessive expansive CA remodelling: AAA, BMI, LDL-C, HDL-C, and higher high-sensitivity C-reactive protein (hs-CRP)). Model 2 was adjusted for the variables in model 1 plus age and current smoking. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated. A higher hs-CRP was defined as hs-CRP > 0.1 mg/dL according to the optimal cut-off value of the receiver operating characteristic curve analysis. A p value < 0.05 was considered significant. All data were analysed using JMP version 12.2 for Windows (SAS Institute, Cary, NC, USA).
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2

Predictors of Acute Decompensated Heart Failure

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Continuous variables were presented as the mean ± standard deviation. The differences between the clinical characteristics and laboratory data of the ADHF and non‐ADHF groups were analysed using the unpaired t‐test or Wilcoxon rank‐sum test. Univariate and multivariate analyses of admission for HF were performed using Cox proportional hazard models. P < 0.05 was considered statistically significant for univariate analysis of the predictors of ADHF. We selected six variables with P values <0.01 for Cox multivariate analysis. Moreover, we used Bonferroni post hoc tests to determine the differences between HFrEF, HFmrEF, and HFpEF at rehospitalization for HF. All data were analysed using JMP Version 12.2 for Windows (SAS Institute, Cary, NC).
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