Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson’s disease: Evidence of shared genetic susceptibility

Danielle Majoor-Krakauer, Ruth Ottman, William G. Johnson, Lewis P. Rowland

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Clinicians have long suspected an association of classic amyotrophic lateral sclerosis (ALS) with Parkinson’s disease (PD), dementia, or both. If proven, this would raise the possibility of a shared genetic susceptibility to the three disorders. To investigate this hypothesis, we compared 151 newly diagnosed ALS patients (seven familial) with 140 controls in terms of cumulative incidence of ALS, PD, and dementia in parents, siblings, and grandparents. We used Cox proportional hazards analysis to compute rate ratios (RRs) for ALS, dementia, and PD in relatives of ALS patients versus relatives of controls. The risk for dementia was significantly higher in relatives of ALS patients than in those of controls (RR = 1.9; 95% Cl 1.1-3.1) and was similar for relatives of patients with sporadic and familial ALS. The risk of PD was higher in relatives of patients with familial ALS (RR = 5.6; 95% Cl 0.6-50.3) than in relatives of patients with sporadic ALS (RR = 1.8; 95% Cl 0.5-6.0), but these differences were not statistically significant, probably due to insufficient statistical power with the available sample size. These findings indicate that ALS and dementia, and perhaps also PD, co-occur within families more often than expected by chance, suggesting that there may be a shared genetic susceptibility to these disorders.

Original languageEnglish (US)
Pages (from-to)1872-1877
Number of pages6
Issue number10
Publication statusPublished - Oct 1994


All Science Journal Classification (ASJC) codes

  • Clinical Neurology

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