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Table 2 Baseline patient characteristics in the NEURO-TTR trial, full analysis set (N = 165)

From: The impact of inotersen on Neuropathy Impairment Score in patients with hereditary transthyretin amyloidosis with polyneuropathy

 

Inotersen (n = 106)

Placebo (n = 59)

Age, mean (SD)

59.6 (12.4)

59.4 (14.1)

Sex, N (%)

 Male

75 (71)

41 (70)

 Female

31 (29)

18 (30)

Mutation Type, N (%)

 V30M

54 (51)

33 (56)

 Non-V30M

52 (49)

26 (44)

FAP stage, N (%)

 Stage 1 (ambulatory without assistance)

71 (67)

42 (71)

 Stage 2 (ambulatory with assistance)

35 (33)

17 (29)

Previous treatment statusa, N (%)

 Pretreatment

62 (59)

35 (59)

 No pretreatment

44 (41)

24 (41)

Cardiomyopathy status, N (%)

 Cardiomyopathy

70 (66)

32 (54)

 No cardiomyopathy

36 (34)

27 (46)

Age of symptom onset, N (%)

 Early onset

31 (29)

20 (34)

 Late onset

75 (71)

39 (66)

NIS, mean (SD)

 Total

46.6 (25.7)

43.4 (24.7)

 Muscle Weakness

21.2 (17.5)

20.0 (16.1)

 Sensation

14.4 (6.3)

13.3 (6.9)

 Reflexes

10.9 (6.0)

10.1 (6.4)

NIS-LL, mean (SD)

 Total

30.1 (15.5)

28.7 (16.0)

 Muscle Weakness

13.9 (11.3)

13.4 (11.0)

 Sensation

10.2 (4.0)

9.8 (4.5)

 Reflexes

6.0 (2.3)

5.6 (2.7)

  1. Abbreviations: FAP familial amyloid polyneuropathy, NIS Neuropathy Impairment Score, NIS-LL Neuropathy Impairment Score – Lower Limb, SD standard deviation
  2. aPrevious treatment with tafamidis and/or diflunisal