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Table 1 Demographics of symptomatic patients according to genotype category

From: A 15-year consolidated overview of data in over 6000 patients from the Transthyretin Amyloidosis Outcomes Survey (THAOS)

 

Overall (n = 4428)

ATTRwt amyloidosis (n = 1410)

V30M early onset

(n = 1082)

V30M late onset

(n = 670)

Non-V30M

(n = 1264)

Male, n (%)

3137 (70.8)

1315 (93.3)

565 (52.2)

433 (64.6)

822 (65.0)

Race/ethnicitya, n (%)

     

 White

2450 (77.2)

1141 (94.1)

263 (68.3)

382 (83.2)

663 (59.5)

 African descent

310 (9.8)

38 (3.1)

33 (8.6)

18 (3.9)

221 (19.8)

 American Hispanic

17 (0.5)

1 (0.1)

10 (2.6)

1 (0.2)

5 (0.4)

 Latino American

136 (4.3)

8 (0.7)

22 (5.7)

4 (0.9)

102 (9.1)

 Asian

245 (7.7)

18 (1.5)

56 (14.5)

53 (11.5)

118 (10.6)

 Other

14 (0.4)

6 (0.5)

1 (0.3)

1 (0.2)

6 (0.5)

Age at enrollment (years), mean (SD)

62.5 (17.22)

77.9 (7.14)

40.6 (9.44)

68.6 (7.94)

60.9 (13.22)

Age at onset of ATTR amyloidosis symptoms (years)

n = 4421

n = 1409

n = 1082

n = 670

n = 1259

 Mean (SD)

56.6 (17.93)

72.3 (9.73)

33.8 (7.19)

63.3 (8.14)

55.0 (13.88)

Time from symptom onset to diagnosis (years)

n = 4069

n = 1337

n = 993

n = 596

n = 1142

 Mean (SD)

4.0 (5.96)

4.6 (6.73)

2.8 (4.74)

3.7 (3.96)

4.4 (6.61)

Follow-up timeb (years), mean (SD)

3.9 (3.20)

2.3 (1.94)

6.8 (3.29)

4.1 (3.03)

3.2 (2.61)

  1. V30M early onset and late onset n based on all patients with available data for disease diagnosis
  2. Symptom onset was the date of first occurrence of symptom(s) reported as definitely related to ATTR amyloidosis
  3. ATTR amyloidosis  transthyretin amyloidosis, ATTRwt amyloidosis wild-type transthyretin amyloidosis, SD  standard deviation
  4. a Denominator for race/ethnicity is the total of non-missing records
  5. b Follow-up time is based on all patients, from enrollment to last observation