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For this analysis, 2,256 relatives positive for at least one BAA on their first screening test were identified, and their baseline screening sample was tested for ZnT8A.
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Baseline screening samples were drawn at time point 0, and blood samples (glucose and insulin) were drawn every 30 minutes for two hours.
Repeat episodes and screening samples were excluded.
Screening samples are taken by GPs.
We then re-tested baseline screening samples and found that 6 volunteers had incorrect HBeAg determination then.
On the basis of baseline screening, the study sample was divided into two groups at baseline: people without cognitive impairment and a group consisting of those with cognitive impairment plus a stratified subsample of those without cognitive impairment.
Ten minutes later a baseline saliva sample was collected.
De-identified plasma samples obtained at a baseline screening visit were recruited from the specimen banks of tuberculosis case-contact studies conducted by the Medical Research Council, The Gambia, West Africa [16] and the Aga Khan University, Karachi, Pakistan [14], respectively.
Baseline screening was conducted before PDT.
Baseline screening was carried out between 1985 and 1988.
A blood sample was obtained at baseline screening for the measurement of total circulating plasma cholesterol.
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