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14% (45.52�C52.77%)), although the specificity was 100%. Sensitivity rose to 76.82% (73.64�C79.79%) when GA?��?17.1% was used as the criterion, but was lower than that achieved when FPG 6.1?mmol/L was used as the criterion (80.93% (77.94�C83.67%)). Compared with the FPG?��?6.1?mmol/L criterion, the specificity of using GA?��?17.1% was also slightly reduced (85.94% (83.86�C87.84%) vs 76.89% (74.42�C79.23%)). JNJ-26481585 mw Use of the combined criteria of either FPG?��?6.1?mmol/L or GA?��?17.1% increased sensitivity to 92.05% (89.89�C93.88%), although both specificity and PPV reduced to 70.15% (67.49�C72.71%) and 65.69% (62.74�C68.55%), respectively. The combined criteria of both FPG?��?6.1?mmol/L and GA?��?17.1% also had high specificity (92.68% (91.07�C94.08%)) INK1197 concentration and PPV (84.79% (81.62�C87.60%)), although sensitivity decreased to 65.70% (62.19�C69.08%). A total of 1058 subjects had GA?��?17.1% or FPG?��?6.1?mmol/L. Of these, 585 subjects met both criteria and, because the PPV was relatively high (84.79% (81.62�C87.60%)), these would be considered to be diabetic. Using these paired values for initial screening, only subjects with FPG?��?6.1?mmol/L and GA?(-)-p-Bromotetramisole Oxalate post-load PG identified significantly more diabetic patients than did FPG testing, especially in Asian populations.14,15 It was reported that 44% of diabetic patients with isolated post-load hyperglycemia, and whose FPG was below the diabetic range (