Table 3.
Trait | Number of cases | h 2 | SE | P value | Kullback‐Leibler R 2 |
---|---|---|---|---|---|
Psychiatric involvement | 214 | 0.55 | 0.19 | 0.0016 | 0.01 ** |
Cerebellar ataxia | 213 | 0.46 | 0.37 | 0.0957 | 0.19 |
Migraine | 214 | 0.77 | 0.33 | 0.0104 | 0.05 * |
Cognition | 205 | 0.46 | 0.91 | 0.1023 | 0.04 |
Dysphonia–dysarthria | 213 | 0.13 | 0.53 | 0.4019 | 0.15 |
Encephalopathy | 214 | 0.64 | 0.36 | 0.0408 | 0.10 |
Stroke‐like episodes | 214 | 0.51 | 0.49 | 0.1423 | 0.12 |
Visual acuity | 210 | 0.26 | 0.26 | 0.2130 | 0.04 |
Ptosis | 213 | 0.15 | 0.39 | 0.3510 | 0.08* |
CPEO | 213 | 0.47 | 0.52 | 0.2102 | 0.06 |
Hearing impairment | 214 | 0.52 | 0.38 | 0.0886 | 0.23* |
Diabetes | 214 | 0.37 | 0.35 | 0.1462 | 0.22 |
Cardiovascular involvement | 193 | 0.08 | 0.36 | 0.4066 | 0.13 |
Converting NMDAS scores to a binary trait leads to a loss of information and, as a result, it was not possible to calculate heritabilities for neuropathy, seizures, gastrointestinal disturbance, or myopathy. Kullback‐Leibler R 2 represents the information gained by including heteroplasmy level and age (*and sex, where P < 0.1) in the model. **Psychiatric involvement was analyzed as a quasi‐quantitative trait to avoid numerical problems in SOLAR, and therefore, this figure represents the proportion of variance due to covariates. Bold indicates significant heritabilities (P < 0.05).