Table 2. Impact of misclassification between schizophrenia (disorder A) and brief psychotic disorder (disorder B) on estimation of genetic parameters from recurrence risks in first-degree relatives.
rgT=0 | rgT=0.25 | rgT=0.5 | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
MTA | MTB | KDA | KD | h2DA | h2DB | rgD | h2DA | h2DB | rgD | h2DA | h2DB | rgD |
0 | 0 | 1.00 | 1.00 | 76 | 21 | 0 | 76 | 21 | 25 | 76 | 21 | 50 |
5 | 5 | 1.00 | 1.00 | 72 | 20 | 25 | 72 | 21 | 44 | 73 | 21 | 63 |
10 | 10 | 1.00 | 1.00 | 68 | 19 | 45 | 69 | 20 | 59 | 69 | 22 | 73 |
15 | 15 | 1.00 | 1.00 | 64 | 19 | 62 | 65 | 21 | 72 | 66 | 23 | 82 |
20 | 20 | 1.00 | 1.00 | 60 | 20 | 75 | 61 | 22 | 81 | 62 | 25 | 88 |
30 | 30 | 1.00 | 1.00 | 51 | 23 | 91 | 53 | 26 | 93 | 55 | 29 | 96 |
0 | 5 | 1.05 | 0.95 | 73 | 21 | 3 | 74 | 21 | 27 | 74 | 21 | 51 |
0 | 10 | 1.10 | 0.90 | 71 | 21 | 6 | 71 | 21 | 29 | 72 | 21 | 52 |
0 | 15 | 1.15 | 0.85 | 68 | 20 | 9 | 69 | 20 | 31 | 70 | 20 | 54 |
0 | 20 | 1.20 | 0.80 | 66 | 20 | 12 | 67 | 20 | 33 | 68 | 20 | 55 |
0 | 30 | 1.30 | 0.70 | 62 | 19 | 17 | 63 | 19 | 37 | 65 | 19 | 57 |
5 | 0 | 0.95 | 1.05 | 75 | 20 | 22 | 75 | 21 | 41 | 75 | 22 | 61 |
10 | 0 | 0.90 | 1.10 | 74 | 20 | 38 | 74 | 21 | 54 | 74 | 22 | 70 |
15 | 0 | 0.85 | 1.15 | 73 | 20 | 52 | 73 | 22 | 64 | 73 | 24 | 77 |
20 | 0 | 0.80 | 1.20 | 71 | 20 | 63 | 71 | 22 | 72 | 71 | 25 | 82 |
30 | 0 | 0.70 | 1.30 | 69 | 22 | 77 | 69 | 25 | 83 | 69 | 28 | 89 |
Parameters for the disorders follow those used in Table 5 of Kendler.5 All values are expressed as percentages. The true disease prevalences are assumed to be 1% for both schizophrenia and brief psychotic disorder, KTA=KTB=1%. True recurrence risks to first-degree relatives are λTA,=8.0, λTB=2.0. These parameters equate to true heritabilities on the liability scale of h2TA=0.76 and h2TB=0.21. MTA is the proportion of true schizophrenia cases misclassified as brief psychotic disorder and MTB is the proportion of true brief psychotic disorder cases misclassified as schizophrenia. The true genetic correlation between the disorders is rgT=0, 0.25,0.5. The estimated parameters based on diagnosed prevalences and recurrences risks have subscript D.