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. 2018 Feb 7;5(3):333–345. doi: 10.1002/acn3.532

Table 3.

Binary trait heritability (h 2)

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).