**Background:** Asian Indians have a high rate of conversion from prediabetes to type 2 diabetes (T2D) and exhibit pronounced postprandial hyperglycemia (PPHG), which increases cardiovascular risk. Dietary strategies targeting PPHG are needed. Previous research by the authors showed that pistachios improved cardiometabolic factors and almonds as a snack improved HbA1c, but effects on postprandial glucose were limited. Only one prior study (Crouch et al., n=20, mixed ethnicity) evaluated premeal almond load, showing a 19.4% reduction in 1-hour postprandial hyperglycemia.
**Methods:** This was a two-phase randomized crossover trial conducted at the National Diabetes, Obesity and Cholesterol Foundation, Delhi, India (January 2018–June 2021). Sixty participants (27 male, 33 female; mean age 41.3±7.9 years; 90% obese) with confirmed prediabetes were enrolled after screening 1317 individuals (1171 screen failures). Phase 1 (OGTT-based): After a 2-week run-in, participants were randomized to treatment-control or control-treatment sequence (30 per period). Treatment: 20 g almonds 30 min before 75 g oral glucose. Control: no food before OGTT. Intravenous blood was collected at −30, 0, 30, 60, 90, and 120 min for glucose, insulin, triglycerides, C-peptide, glucagon, GLP-1, and DPP-4. Phase 2 (CGMS-based): Free-living, open-label crossover. Participants wore iPro2 CGM device for 3 days. Treatment: 20 g almonds 30 min before each major meal (60 g/day). Control: standard diet without premeal almonds. CGMS recorded 288 readings/24 h. Glycemic variability (MAGE, SD, MoDD) and glycemic control parameters (mean 24-h glucose, time in range, AUC above 7.8 mmol/L, peak glucose, minimum night glucose, PPHG AUC, total AUC) were assessed. Washout period was 7 days between phases. Dietary compliance was 90%.
**Key Results:** Phase 1 (OGTT): The overall AUC (0–2 h) for blood glucose was significantly lower with premeal almond load vs. control (1057.1±101.7 vs. 1290.0±134.0, p<0.001). Mean blood glucose at 30, 60, 90, and 120 min was significantly lower (p<0.001 for all). PPHG was reduced by 18.05% in AUC on OGTT, 24.8% at 1-hour, and 28.9% at 2-hour post OGTT. Serum insulin AUC (412.2±135.6 vs. 406.2±163.8 pmol/L, p<0.001), C-peptide AUC (0.9±0.3 vs. 1.3±0.5 nmol/L, p<0.001), and plasma glucagon AUC (159.3±69.9 vs. 157.3±68.2 pmol/L, p<0.001) were significantly lower with treatment. Serum triglycerides, GLP-1, and DPP-4 did not differ significantly between diets. Phase 2 (CGMS): Premeal almond load significantly improved mean 24-h blood glucose (M) (−0.4 mmol/L, 95% CI: −0.6 to −0.3, p<0.001). Time spent above 7.8 mmol/L was lower (−0.04 h, p<0.001) with corresponding AUC reduction (−53.7 mmol/h/L, 95% CI: −78.1 to −29.2, p<0.001). Peak 24-h glucose decreased (−0.8 mmol/L, p<0.001) and minimum night glucose decreased (−0.4 mmol/L, p<0.001). PPHG AUC pp decreased by 10.07% (−51.8 mmol/h/L, 95% CI: −96.6 to −6.9, p=0.02). Overall hyperglycemia AUC total decreased (−43.3 mmol/h/L, 95% CI: −67.4 to −19.1, p<0.001). Glycemic variability improved: SD of mean glucose concentration (−0.1, p=0.02) and MoDD (−0.1, p<0.001). MAGE showed non-significant improvement (p=0.06). Basal hyperglycemia AUC did not differ (p=0.727).
**Clinical Implications:** This study demonstrates that a simple, low-cost dietary intervention—consuming 20 g of almonds 30 minutes before each major meal—significantly reduces postprandial hyperglycemia and improves multiple measures of glycemic control and variability in Asian Indians with prediabetes. The 18.05% reduction in glucose AUC on OGTT and 10.07% reduction on CGMS, along with improvements in insulin, C-peptide, and glucagon levels, suggest this strategy may help delay progression from prediabetes to T2D. Given the high prevalence of prediabetes and PPHG in Asian Indians, and the association between postprandial glucose excursions and cardiovascular risk, this intervention has broad public health implications. The findings are generalizable to the substantial population with prediabetes in India. Limitations include the short-term nature of the study (3 days CGMS), lack of formal sample size calculation for Phase 2, and the open-label design for the CGMS phase. Longer-term studies are needed to assess effects on diabetes prevention and cardiovascular outcomes.