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. Author manuscript; available in PMC: 2021 Jul 1.
Published in final edited form as: Clin Gastroenterol Hepatol. 2019 Dec 4;18(8):1812–1821.e7. doi: 10.1016/j.cgh.2019.11.043

Table 3:

Predicted trends for longitudinal measurements of fasting glucose, HbA1c and weight among patients with incident diabetes, by case status and race/ethnicity

Total (N=110,699) Asian (N=14,836) Black (N=14,730) Hispanic (N=36,892) White (N=44,241)

Pancreatic Cancer No Pancreatic Cancer Pancreatic Cancer No Pancreatic Cancer Pancreatic Cancer No Pancreatic Cancer Pancreatic Cancer No Pancreatic Cancer Pancreatic Cancer No Pancreatic Cancer





Parameter1 Estimate (CI)2 Estimate (CI)2 p3 Estimate (CI)2 Estimate (CI)2 p3 Estimate (CI)2 Estimate (CI)2 p3 Estimate (CI)2 Estimate (CI)2 p3 Estimate (CI)2 Estimate (CI)2 p3 p4
Glucose (mg/dL)
 Slope 3 yrs-1 mo 1.19 (0.71–1.67) 0.81 (0.78–0.84) 0.06 1.70 (0.50–2.90) 0.91 (0.84–0.97) 0.27 −0.20 (−1.55–1.16) 0.88 (0.79–0.97) 0.14 1.38 (0.34–2.43) 1.01 (0.95–1.06) 0.45 1.62 (0.90–2.33) 0.80 (0.75–0.84) 0.03 0.16
 Change in slope at 1 mo 37.47 (31.51–43.43) 27.68 (27.38–27.97) <0.01 34.49 (18.57–50.42) 18.98 (18.32–19.63) 0.07 44.65 (24.36–64.95) 27.46 (26.57–28.36) 0.11 30.94 (20.87–41.01) 29.99 (29.42–30.57) 0.85 38.98 (30.53–47.43) 28.72 (28.29–29.14) 0.02 0.28
HbA1c (%)
 Slope 3 yrs-1 mo 0.03 (0.00–0.06) 0.04 (0.04–0.04) 0.38 0.03 (−0.12–0.19) 0.03 (0.03–0.04) 0.05 0.01 (−0.05–0.08) 0.04 (0.03–0.04) 0.41 0.01 (−0.05–0.07) 0.04 (0.04–0.04) 0.24 0.04 (0.01–0.08) 0.04 (0.03–0.04) 0.84 0.31
 Change in slope at 1 mo 1.39 (1.12–1.67) 0.86 (0.85–0.87) <0.001 0.92 (0.43–1.41) 0.62 (0.59–0.64) 0.09 1.37 (0.74–2.00) 0.93 (0.90–0.97) 0.20 1.27 (0.81–1.74) 1.01 (0.99–1.04) 0.15 1.48 (1.05–1.91) 0.79 (0.78–0.81) <0.01 0.72
Weight (kg)
 Slope 3 yrs-diagnosis −0.18 (−0.44–0.08) 0.33 (0.31–0.34) <0.001 −0.19 (−0.49–0.11) 0.23 (0.20–0.26) <0.01 0.24 (−0.39–0.87) 0.40 (0.36–0.44) 0.67 −0.30 (−0.70–0.09) 0.31 (0.28–0.33) <0.01 −0.16 (−0.61–0.28) 0.35 (0.32–0.37) 0.03 0.65
1

Metabolic markers were evaluated from diabetes diagnosis up to three years prior in six-month intervals.

2

From a GEE model with the metabolic characteristic as a continuous outcome variable (identity link), time period as the main exposure, age, gender and race as covariates, and patient as the clustering variable. Glucose and HbAlc models included a spline term at the 6–1 month time interval to model the change in slope. Models were run separately for cases and non-cases.

3

P-value for heterogeneity across cases and non-cases. Obtained from a GEE model with a time period*case status interaction term. Glucose and HbAlc models included an additional interaction term for change in slope*case status.

4

P-value for heterogeneity across cases status and race. Glucose and HbA1c models included an additional three-way interaction for change in slope*case status*race. Glucose and HbAlc models also included three-way interaction for change in slope.