Skip to main content
. 2023 Oct 4;29(11):2902–2908. doi: 10.1038/s41591-023-02576-1

Table 1.

Characteristics of the trial participants at baseline

All participants (n = 96) Treatment group (n = 47) Placebo group (n = 49)
Age, years (s.d.) 11.1 (2.4) 11.5 (2.3) 10.7 (2.5)
Females, n (%)a 40 (41.7) 19 (40.4) 21 (42.9)
Body mass index, kg m2 (s.d.) 17.9 (2.7) 18.0 (2.7) 17.7 (2.7)
HbA1c at diagnosis, mmol mol−1 (s.d.) 105.8 (23.7) 110 (25.9) 102 (21.1)
HbA1c at diagnosis, % (s.d.) 11.8 (4.3) 12.2 (4.5) 11.5 (4.1)
Diabetic ketoacidosis at onset, % 12.5 10.6 14.3
Enterovirus presentb 0 0 0
Anti-glutamic acid decarboxylase, n (%) 80 (83) 39 (83) 41 (84)
Islet antigen 2 antibodies, n (%) 74 (77) 35 (74) 39 (80)
Anti-insulin antibodies, n (%) 64 (67) 28 (60) 36 (73)
Anti-zinc transporter protein 8 antibodies, n (%) 77 (80) 37 (79) 40 (82)
0 antibodies, n (%) 1 (1) 1 (2.1) 0 (0)
1 antibody, n (%) 8 (8) 4 (8.5) 4 (8.2)
2 antibodies, n (%) 16 (17) 10(21.3) 6 (12.2)
3 antibodies, n (%) 29 (30) 13 (27.7) 16 (32.7)
4 antibodies, n (%) 42 (44) 19 (40.4) 23 (46.9)
Start of antiviral therapy, days from diagnosis (s.d.) 17.8 (3.2) 18.1 (3.2) 17.6 (3.2)

aSex was reported by a pediatrician based on clinical examinations and interview with the participants.

bRT–PCR analyses of saliva, nasopharyngeal aspiration, nasal swab and feces.