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Spss statistic for windows version 25

Manufactured by IBM
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SPSS Statistics for Windows, version 25.0 is a software application designed for statistical analysis. It provides a suite of tools for data management, analysis, and presentation. The software is intended to assist users in organizing, analyzing, and interpreting data efficiently.

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Lab products found in correlation

7 protocols using spss statistic for windows version 25

1

Sociodemographic Risk Factors for Mental Health

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Data were analyzed using SPSS Statistic for Windows, version 25.0 (IBM Corp., Armonk, N.Y., USA). Data normality was evaluated using one-sample Kolmogorov-Smirnov test and was presented as mean ± standard deviation (SD) for normally distributed data, median [interquartile range (IQR)] for skewed data, and frequency (percentage) for nominal data. To identify the risk factors for depression, anxiety, and stress, two steps logistic regression analysis was used. First, univariate regression was used to identify each sociodemographic variable that was associated with depression, anxiety, and stress. Variables with p-value < 0.25 [38 (link)] were then subjected to multivariate regression using backward selection method. Variables with p-value < 0.05 from the multivariate regression analysis were considered as independent risk factors. During the logistic regression analysis, variables with missing data of more than 20% were excluded, and depression, anxiety, and stress variables were re-categorized as dichotomous (normal or not) variables with the cut-off scores as follows: 9 for depression, 6 for anxiety, and 10 for stress [36 ].
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2

Multivariate Analysis of Fatty Acid Composition

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Statistical analysis was performed using GraphPad Prism 6.01 Software (San Diego, CA, USA). One-way analysis of variance (ANOVA with a Tukey’s HSD post hoc test) was used to compare the existence of significant differences amongst the chemical profiles. Concerning the cellular assays, the level of significance between different treatment groups relative to control was determined by one-way analysis of variance (ANOVA), followed by Bonferroni test. Values of p ≤ 0.05 were considered statistically significant.
Principal component analysis (PCA) was carried out using IBM SPSS Statistic for Windows version 25.0 (Armonk, NY, USA) and was applied to data obtained from three replicates, to inspect if the ordination of species could be related to fatty acid composition. PCA is a method that indicates (indirect) gradients by producing a smaller set of variables (principal components) that explain the variability of a larger set of variables [47 (link)]. PCA was applied to fatty acid composition (μg mg−1 dry extract): C12:0, C13:0, C14:1n-5c, C14:0, C15:1n-5, C15:0, C16:1n-7, C16:0, C17:1n-7, C17:0, C18:3n-6c, C18:2n-6c, C18:1n-9c, C18:1n-9t, C18:0, C20:4n-6, C20:5n-3, C20:3n-6, C20:2n-6, C18:3n-3c, C20:0, C21:0, C22:6n-3, C18:2n-6t, C22:1n-9, C22:0 and n-6/n-3.
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3

Determinants of Childhood Undernutrition

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Acquired data was analysed using SPSS Statistic for Windows, version 25.0 (IBM Corp., Armonk, N.Y., USA). Data analysis was conducted in two phases. In the first phase, univariate logistic regression was used to identify independent variables that were associated with stunting or underweight. Variables with p < 0.1 were included in the next phase. In second phase, multivariate logistic regression using backward selection was used. Variables with p <0.05 from multivariate analysis were considered as the determinants.
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4

Statistical Analysis of Quantitative Variables

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Statistical analyses were performed using IBM SPSS Statistic for Windows, Version 25.0 (Armonk, NY: IBM Corp.) Normal distribution of continuous quantitative variables was assessed by Kolmogorov–Smirnov test. Continuous variables were presented as means with standard deviations (SD) or median (interquartiles (IQR)) for skewed variables. Categorical variables were presented as numbers with percentages. Feasibility was evaluated as the percentage of patients enrolled in whom measurements were obtained. Comparison between parameters and techniques was done using paired—T test, Mann–Whitney U Test and Pearson correlation. Bland–Altman analyses was performed in order to assess the bias and limits of agreement (LOA) (defined as ±1.96 SD). Intraclass correlation coefficient (ICC) was used to determine the intra- and inter-observer variability and the inter-technique variability and 95% confidence intervals (CI) were calculated. Statistical significance was considered for a p-value < 0.05.
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5

Analyzing SF-MPQ-2 Scores: Data Quality and Screening

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The SF-MPQ-2 total and subscale scores were considered as interval variables. Data quality and screening, including the percentage of missing data, outliers, and presence of floor/ceiling effects was performed. Respondents with two or more missing items were excluded, in line with the developers’ instructions [21 (link)]. Continuous variables were descriptively summarized using means and standard deviations while percentages were used to report categorical variables. The data were then examined for normality with histograms, and the Shapiro–Wilk test. All statistical analyses were completed with Microsoft Excel Version 2013 and SPSS statistic for Windows™, Version 25.0. (Armonk, NY: IBM Corp, Released 2017).
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6

Comparing Postprandial Glucose and Insulin Responses

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The SPSS software was used for all statistical analysis (IBM SPSS statistic for Windows, version 25, IBM corp., Armonk, NY, USA, 2017). Categorical variables were reported as frequency and percentage. Normality was assessed by the Kolmogorov–Smirnov test and with a histogram. Continuous variables are presented as the medians and interquartile ranges (IQR) or the mean ± standard deviation (SD) as appropriate. Chi-squared tests or Fisher’s exact test were used for categorical variables as appropriate. GI variations between the formulas were evaluated by the Kruskal–Wallis test. Because each of the tested formulas was given to each participant, the Friedman test and the Wilcoxon test were applied to compare postprandial glucose and insulin levels between the different solutions.
The glycemic index was calculated using the area under the curve over the baseline, excluding the area beneath the baseline (incremental area under the curve [IAUC]), as recommended by the Food and Agriculture Organization, which was assessed as the sum of the trapezium, relative to the IAUC after reference food consumption (glucose solution) [14 (link)]. All statistical tests were two tailed, and a p value < 0.05 was considered significant.
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7

Inflammatory and Mitochondrial Markers in Sepsis

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Statistical analysis was performed with the SPSS statistic for Windows, Version 25 (IBM Corp, Armonk, NY, USA). A student’s t-test was performed to assess whether there were significant differences in the physical variables between ICU patients and the distribution of inflammatory and mitochondrial function markers. The easyROC: a web-tool for ROC curve analysis (V. 1.3.1) performed the ROC analysis, and the cut-off method used was the Youden method. Logistic regression analysis was used to evaluate the univariate and multivariate association between the septic status (positive versus negative) and the markers of inflammatory and mitochondrial function. The odds ratio (OR) was used as an index of association strength and the 95% confidence limits (95% CL) were calculated. Statistics with p < 0.05 were considered statistically significant. All statistical tests were two-tailed.
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