Table 1.
All patients | NGT | HG‐T1DR | HG‐PCR | HG‐UND | p value | |
---|---|---|---|---|---|---|
N | 223 | 176 | 17 | 10 | 20 | n/a |
% of total (223) | n/a | 78.9 | 7.6 | 4.5 | 9 | n/a |
% of HG (47) | n/a | n/a | 36.2 | 21.3 | 42.6 | n/a |
Sex (F‐M) | 106–117 | 89–87 | 8–9 | 1–9 | 8–12 | p=0.14941 |
White not Hispanic, n (%) | 117 (52.5) | 96 (54.5) | 9 (52.9) | 5 (50.0) | 7 (35.0) | p=0.30282 |
White Hispanic, n (%) | 83 (37.2) | 63 (35.8) | 8 (47.1) | 3 (30.0) | 9 (45.0) | n/a |
African‐American, n (%) | 22 (9.9) | 16 (9.1) | 0 | 2 (20.0) | 4 (20.0) | n/a |
Other, n (%) | 1 (0.4) | 1 (0.6) | 0 | 0 | 0 | n/a |
Age at T1D onset mean ± SD (years) | 14 ± 8.6 | 14.3 ± 8.4 | 13.9 ± 10.7 | 9.1 ± 5.3 | 14.7 ± 8.8 | p=0.3159a |
Range (years) | 0–39 | 0–38 | 2–39 | 1–17 | 4–32 | n/a |
Patients with no available data | 2 | 1 | 0 | 0 | 1 | n/a |
T1D duration at transplantation mean ± SD (years) | 26.6 ± 8.6 | 27.5 ± 8.4 | 20.9 ± 10.0 | 27.6 ± 5.0 | 23.1 ± 7.8 | p = 0.0161 |
Range (years) | 2–50 | 3–50 | 2–39 | 22–35 | 8–36 | n/a |
Patients with no available data | 2 | 1 | 0 | 0 | 1 | n/a |
Age at transplant mean ± SD (years) | 40.7 ± 8.0 | 41.8 ± 8.1 | 34.8 ± 6.6 | 36.6 ± 4.4 | 38.2 ± 6.3 | p = 0.0006 |
Range (years) | 23–60 | 23–60 | 23–47 | 30–44 | 29–50 | n/a |
Length of follow‐up mean ± SD (years) | 6.2 ± 4.1 | 6.2 ± 4.2 | 6.8 ± 3.8 | 4.5 ± 2.9 | 6.2 ± 4.4 | p = 0.5029* |
Range (years) | 1.0–22.6 | 1.0–22.6 | 2.2–17.2 | 2.1–10.3 | 1.1–15.6 | n/a |
Last HbA1c on follow‐up mean ± SD | 5.7 ± 0.7 | 5.5 ± 0.4 | 6.9 ± 0.9 | 6.9 ± 1.1 | 7.1 ± 0.8 | p < 0.0001 |
Patients with no available data | 54 | 32 | 12 | 7 | 3 | n/a |
HG‐PCR, hyperglycemia with pancreas chronic rejection; HG‐T1DR, hyperglycemia with type 1 diabetes recurrence; NGT, normal glucose tolerance.
Overall p values of the chi‐square test are shown for independence between sex1 or ethnicity2 (excluding “other”) and group classification (NGT, HG‐T1DR, HG‐PCR, HG‐UND).
One‐ way analysis of variance (Global Kruskal–Wallis test).