Skip to main content
. 2021 Dec 14;12:793762. doi: 10.3389/fimmu.2021.793762

Table 1.

The clinical characteristics of included children.

Total CD VD P
N Values N Values N Values
Birth
Sex [boy, %] 2079 1182 (56.85%) 987 568 (57.55%) 1092 614 (56.23%) 0.54
Age [mean ± sd, months old] 2079 36.97 ± 40.27 987 36.5 ± 41.11 1092 37.4 ± 39.5 0.61
Premature delivery [yes, %] 2079 222 (10.68%) 987 157 (15.91%) 1092 65 (5.95%) <0.01
Father’s allergic diseases [yes, %] 2079 384 (18.47%) 987 189 (19.15%) 1092 195 (17.86%) 0.45
Maternal allergic diseases [yes, %] 2079 294 (14.14%) 987 131 (13.27%) 1092 163 (14.93%) 0.28
Other family members’ allergic diseases [yes, %] 2079 149 (7.17%) 987 72 (7.29%) 1092 77 (7.05%) 0.83
Postnatal exposure
Exclusive breastfeeding [yes, %] 2079 658 (31.65%) 987 267 (27.05%) 1092 391 (35.81%) <0.01
Exposure to smoke [yes, %] 2079 391(118.81%) 987 193 (19.55%) 1092 198 (18.13%) 0.41
Outcomes
First episode of wheezing [yes, %] 2079 724 (34.82%) 987 367 (37.18%) 1092 357 (32.69%) 0.03
Length of time for development of FTW [mean ± sd, months] 724 18.33 ± 20.34 367 17.78 ± 20.33 357 18.90 ± 20.37 0.46
Recurrent wheeze [yes, %] 2079 417(20.06%) 987 207 (20.97%) 1092 210 (19.23%) 0.32
Asthma [yes, %] 2076 267 (12.84%) 985 146 (14.82%) 1091 121 (11.09%) 0.01
Length of time for development of asthma [mean ± sd, months] 267 48.35 ± 31.45 146 48.47 ± 32.95 121 48.20 ± 29.67 0.94
LOS [mean ± sd, day] 2079 6.60 ± 6.40 987 6.35 ± 5.43 1092 6.8 ± 7.09 0.1
LOS for wheezing diseases (not asthma) [mean ± sd, day] 503 6.01 ± 4.71 347 6.03 ± 4.86 256 5.97 ± 4.47 0.93
Test of immune cells
CD3+ 1697 3418.35 ± 2868.99 807 3343.25 ± 2725.54 890 3486.45 ± 2993.02 0.3
CD3+% 1697 63.62 ± 11.67 807 63.09 ± 11.73 890 64.09 ± 11.59 0.08
CD3+CD4+ 1697 1823.26 ± 1258.3 807 1816.42 ± 1245.17 890 1829.46 ± 1270.76 0.83
CD3+CD4+% 1697 35.55 ± 10.79 807 35.72 ± 11.01 890 35.39 ± 10.59 0.54
CD3+CD8+ 1697 1368.33 ± 2107.98 807 1305.32 ± 1939.54 890 1425.46 ± 2249.41 0.24
CD3+CD8+% 1697 23.25 ± 11.9 807 22.62 ± 11.69 890 23.83 ± 12.07 0.04
CD4/CD8 1697 1.93 ± 1.21 807 2.01 ± 1.33 890 1.86 ± 1.07 0.01
CD3+/HLA-DR+ 1388 590.98 ± 1864.55 664 582.02 ± 1796.89 724 599.19 ± 1925.72 0.86
CD3+/HLA-DR+% 1404 8.2 ± 21.64 669 7.7 ± 12.41 735 8.65 ± 27.47 0.4
Treg 1421 129.4 ± 108.52 677 133.02 ± 117.85 744 126.11 ± 99.24 0.23
Treg% 1440 3.56 ± 18.92 683 3.59 ± 16.07 757 3.54 ± 21.18 0.96
CD3-/CD19+ 1697 1135.12 ± 876.03 807 1119.8 ± 853.2 890 1149.02 ± 896.47 0.49
CD3-/CD19+% 1697 23.05 ± 10.61 807 23.39 ± 10.89 890 22.74 ± 10.34 0.21
CD45+ 1697 5231.69 ± 3734.08 807 5112.76 ± 3529.76 890 5339.53 ± 3908.98 0.21
NK 1697 618.8 ± 589.15 807 600.75 ± 517.67 890 635.17 ± 647.03 0.22
NK% 1697 12.03 ± 7.42 807 12.14 ± 7.26 890 11.93 ± 7.55 0.55
CD14+/HLA-DR+ 1389 898.21 ± 1476.54 665 848.34 ± 659.08 724 944.01 ± 1944.77 0.21
CD14+/HLA-DR+% 1408 84.94 ± 29.44 671 84.12 ± 23.05 737 85.67 ± 34.24 0.32

CD, caesarean delivery; VD, vaginal delivery; sd, standard deviation; N, Number of sample size.CD3+, The number of CD3+ T cells/ul; CD3+%, The ratio of CD3+ T cell in total lymphocyte; CD3+CD4+, The number of CD3+CD4+ T cells/ul; CD3+CD4+%, The ratio of CD3+CD4+ T cell in total lymphocyte; CD3+CD8+, The number of CD3+CD8+ T cells/ul; CD3+CD8+%, The ratio of CD3+CD8+ T cell in total lymphocyte; CD4/CD8, the ratio of CD4+ T cell versus CD8+ T cell; CD3+/HLA-DR+, The number of CD3+/HLA-DR+ T cells/ul; CD3+/HLA-DR+%, The ratio of CD3+/HLA-DR+ T cell in total lymphocyte; Treg, The number of regulatory T cells/ul; Treg%, The ratio of regulatory T cell in total lymphocyte; CD3-/CD19+, The number of B cells/ul; CD3-/CD19+%, The ratio of B cell in total lymphocyte; CD45+, The number of CD45+ cells/ul; NK, The number of NK cells/ul; NK%, The ratio of NK cell in total lymphocyte; CD14+/HLA-DR+, The number of activated monocytes cells/ul; CD14+/HLA-DR+%, The ratio of activated monocytes in total monocytes.

All tests of these cells are done by flow cytometry. The absolute number (cells/µL) of positive cells in the sample can be determined by comparing cellular events to bead events. Absolute counts of cells are calculated by BD FACSCanto clinical software using the following formula: cell population absolute count test volume = (events in cell population/events in absolute count bead region)*(beads of each test/test volume).

In bold <0.01: P values less than 0.01.