Skip to main content
. Author manuscript; available in PMC: 2021 Dec 12.
Published in final edited form as: Nat Med. 2021 Sep 23;27(10):1818–1824. doi: 10.1038/s41591-021-01505-4

Table 1 |.

Baseline participant characteristics, by arm

Placebo n = 90 Valsartan n = 88
Mean age*, years 23.5 (10.1) 23.1 (10.1)
 18 years of age or younger, n (%) 39 (43%) 38 (43%)
 Pre-puberty*, n (%) 20 (22%) 19 (22%)
Female*, n (%) 35 (39%) 34 (39%)
White*, n (%) 88 (98%) 85 (97%)
Black, n (%) 0 3 (3%)
Unknown, n (%) 2 (2%) 0
Hispanic, n (%) 21 (23%) 15 (17%)
Sarcomeric gene*, n (%)
  MYH7 36 (40%) 25 (28%)
  MYBPC3 44 (49%) 47 (53%)
  TNNT2 3 (3%) 5 (6%)
  TNNI3 2 (2%) 3 (3%)
  TPM1 1 (1%) 4 (5%)
  MYL2 1 (1%) 1 (1%)
  MYL3 2 (2%) 1 (1%)
  ACTC 1 (1%) 2 (2%)
Mean BSA, m2 1.85 (0.35) 1.82 (0.34)
Mean BMI* 25.6 (5.9) 25.0 (5.6)
Systolic blood pressure*, mmHg 118 (13) 118 (10)
Diastolic blood pressure, mmHg 69 (11) 68 (10)
NYHA*: Class I, n (%) 84 (93%) 80 (91%)
   Class II, n (%) 6 (7%) 8 (9%)
BSA-adjusted z-score for maximum LV wall thickness (participants ≤18 years) 8.1 (4.6) 8.2 (5.1)
Maximum LV wall thickness, mm (participants >18 years) 16.4 (3.4) 17.9 (4.7)
LVEF*, % 66.3 (7.2) 66.1 (5.8)
Beta blocker use*, n (%) 14 (16%) 18 (20%)
Calcium channel blocker use*, n (%) 1 (1%) 4 (5%)

Numbers are mean and standard deviation, unless otherwise indicated.

*

Variables pre-specified to be adjusted in the analysis model. Because of sparse categories, race was dichotomized to white versus non-white, and genotype was dichotomized to thick filament genes (MYBPC3, MYH7, MYL2 or MYL3) versus thin filament genes (ACTC, TNNT2, TNNI3 or TPM1). One participant in the placebo group was missing LVEF.