Journal of Translational Medicine (Jun 2021)

Nomogram for short-term outcome assessment in AChR subtype generalized myasthenia gravis

  • Rui Zhao,
  • Ying Wang,
  • Xiao Huan,
  • Huahua Zhong,
  • Zhirui Zhou,
  • Jianying Xi,
  • Yuwei Da,
  • Lin Lei,
  • Ting Chang,
  • Zhe Ruan,
  • Lijun Luo,
  • Shengnan Li,
  • Huan Yang,
  • Yi Li,
  • Sushan Luo,
  • Chongbo Zhao

DOI
https://doi.org/10.1186/s12967-021-02961-9
Journal volume & issue
Vol. 19, no. 1
pp. 1 – 10

Abstract

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Abstract Background An accurate prediction for prognosis can help in guiding the therapeutic options and optimizing the trial design for generalized myasthenia gravis (gMG). We aimed to develop and validate a predictive nomogram to assess the short-term outcome in patients with the anti-acetylcholine receptor (AChR) subtype gMG. Methods We retrospectively reviewed 165 patients with AChR subtype gMG who were immunotherapy naïve at the first visit from five tertiary centers in China. The short-term clinical outcome is defined as the achievement of minimal symptom expression (MSE) at 12 months. Of them, 120 gMG patients from Huashan Hospital were enrolled to form a derivation cohort (n = 96) and a temporal validation cohort (n = 24) for the nomogram. Then, this nomogram was externally validated using 45 immunotherapy naïve AChR subtype gMG from the other four hospitals. Multivariate logistic regression was used to screen independent factors and construct the nomogram. Results MSE was achieved in 70 (72.9%), 20 (83.3%), and 33 (73.3%) patients in the training, temporal validation, and external validation cohort, respectively. The duration ≤ 12 months (p = 0.021), ocular score ≤ 2 (p = 0.006), QMG score > 13 (p = 0.008), and gross motor score ≤ 9 (p = 0.006) were statistically associated with MSE in AChR subtype gMG. The nomogram has good performance in predicting MSE as the concordance indexes are 0.81 (95% CI, 0.72–0.90) in the development cohort, 0.944 (95% CI, 0.83–1.00) in the temporal validation cohort, and 0.773 (95% CI, 0.63–0.92) in the external validation cohort. Conclusion The nomogram achieved an optimal prediction of MSE in AChR subtype gMG patients using the baseline clinical characters.

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