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The increased score value ('3' in this example) was used as the reference level (S1, i in equation (1)) for subsequent visits to describe any relative change of severity (decrease or increase) with respect to the visit of addition (the 'reference visit').
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The directionality of scores was adjusted so that increased score values reflected increased anxiety-like emotionality.
For determining TDC, the clinician not only considered the basic reference items but actually increased score values could also yield added reference items (see above, section 'Background of TDC').
Scores per item (proportion of studies with the item completely reported) were considered for assessing the risk of bias across studies (risk of bias decreases with increasing score values), as was a funnel plot representing study size against the incidence of ADE.
By linear regression, the presence of one T allele increased the score value (analyzed here as a continuous variable) in 1.4 points (p = 0.038).
The scoring system was then applied to the validation group showing that the incidence of GDM increased with increasing clinical score values ranging from 0.9 in women who scored ≤1 to 18.7% in women who scored ≥6.
Differences between scores on baseline and follow-up measures were the assessment of effect considered, so that positive values indicated increased scores.
Increasing score indicates the severity of injury.
The x-axis features date samples ordered by increasing PC1 score values whilst the y-axis features metabolites ordered by two criteria: First metabolite classes were ordered by their median loading value then the metabolites were ordered by their loading values within each class.
The probability of having a positive IGRA increases with score value.
When an increase in score value is sustained and a basic reference item is not involved, the item with the sustained larger score during treatment will likely also have a large score value in the data from the assessor following treatment.
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