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. 2021 Jan 8;143(12):3589–3602. doi: 10.1093/brain/awaa323

Table 3.

Mean change and SRM of CMTESv2, CMTESv2-R and CMTPedS in AD-CMT2A and AR-CMT2A at 1- and 2-years follow-up

Follow-up, years n Baseline Change P SRM
Autosomal dominant
 CMTESv2 1 38 10.66 ± 5.94 0.84 ± 2.42 0.039 0.35
 CMTESv2R 1 38 14.53 ± 6.96 0.63 ± 3.19 0.230 0.20
 CMTESv2 2 34 9.47 ± 6.26 0.97 ± 1.77 0.003 0.55
 CMTESv2-R 2 34 13.00 ± 7.68 1.21 ± 2.52 0.009 0.48
Autosomal recessive
 CMTESv2 1 6 12.33 ± 6.65 0.17 ± 3.06 0.900 0.05
 CMTESv2-R 1 6 17.00 ± 7.21 −0.33 ± 2.73 0.777 −0.12
 CMTESv2 2 4 10.25 ± 7.23 0.25 ± 1.26 0.718 0.20
 CMTESv2-R 2 4 14.75 ± 7.63 0 ± 1.41 1.000 0
 CMTESv2 4 5 13.40 ± 6.66 1.80 ± 3.11 0.266 0.58
 CMTESv2R 4 5 17.60 ± 7.23 1.40 ± 3.91 0.468 0.36
Autosomal dominant and autosomal recessive
 CMTPedS 1 17 25.41 ± 8.01 2.24 ± 3.09 0.009 0.72
 CMTPedS 2 7 28.86 ± 7.82 4.00 ± 3.79 0.031 1.06

The CMTESv2 changed significantly over 1 and 2 years in patients with AD-CMT2A, whereas the CMTESv2-R changed significantly over 2 years. The CMTPedS (all cases grouped) changed significantly both over 1 and 2 years. There was no significant change in cases with AR-CMT2A over 1 and 2 years. Mean changes that are statistically significance have their P-values and SRMs highlighted in bold. Data shown represent mean ± SD.