You are viewing the site in preview mode

Skip to main content

Table 2 Clinical characteristics comparing children with and without a rare genetic variant

From: Psychopharmacology in children with genetic disorders of epigenetic and chromatin regulation

 

Any genetic variant

No genetic variant reported

p

n

32 (10%)

299 (90%)

 

Demographic characteristics

 Female Sex, N(%)

9 (28%)

48 (16%)

0.1

 Age at first visit, Mean (SD)

11.0 (3.1)

10.6 (3.1)

0.5

 Number of follow-up visits, Mean (SD)

8.2 (5.0)

8.2 (6.3)

0.9

 Follow-up time in years, Mean (SD)

3.8 (3.2)

3.4 (3.1)

0.5

Co-occurring developmental and psychiatric conditions

 Intellectual Disability, N (%)

18 (56%)

92 (31%)

0.007*

 Autism diagnosis, N (%)

26 (81%)

274 (94%)

0.09

 ADHD diagnosis, N (%)

16 (50%)

171(57%)

0.5

 Non-speaking, N (%)

11 (34%)

68 (23%)

0.2

 Past crisis service use for behaviour, N (%)

4 (13%)

47 (16%)

0.8

 Aggressive behaviour, N (%)

22 (69%)

215 (72%)

0.7

 Self-injurious behaviour, N (%)

14 (44%)

140 (47%)

0.8

Medical history

 Number of subspecialist physicians, Mean (SD)

3.3 (2.6)

1.2 (1.4)

 < 0.001

 Number of physical health conditions, Mean (SD)

1.6 (0.9)

1.1 (0.5)

 < 0.001

 Seizures, N (%)

13 (40%)

34 (11%)

 < 0.001

 Obesity, N (%)

12 (38%)

84 (28%)

0.3

 Asthma, N (%)

2 (6%)

12 (4%)

0.6

 GERD, N (%)

7 (22%)

7 (2%)

 < 0.001*

 Chronic constipation, N (%)

2 (6%)

16 (5%)

0.7

  1. P-values from Fisher’s exact test or Chi-squared for counts/proportions, means/medians are compared with t-test (for normally distributed data) or Mann-Whitney U test (for non-parametric distributions). Results are reported uncorrected. GERD: gastroesophageal reflux disease