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. 2019 Apr 8;68(3):885–923. doi: 10.3233/JAD-181089

Table 3.

Co-morbidities in young apolipoprotein ɛ4 carriers

Subjects / Age Sample Size Sex Study Scope Major Finding Citation Quality of Evidence
Meta-analysis of 28 studies on schizophrenia; Age of subjects not specified Not specified Mixed Determine the association between APOE and schizophrenia: evidence of systematic review and updated meta-analysis Protective effect was found for ɛ3 in the Asian population (OR = 0.73, 95% CI = 0.54–0.98) Gonzalez-Castro et al. [70] Moderate
Infants with hypoxic-ischemic encephalopathy ɛ4 Carriers (N = 41) Mixed APOE genotype and outcome in infants with hypoxic-ischemic encephalopathy Disability was not associated with APOE genotype in this cohort of hypoxic-ischemic encephalopathy patients Cotton et al. [72] Moderate
Pooled analysis of 15 studies on the association of APOE alleles with age-related macular degeneration; Age not specified Not specified Mixed Evidence of association of APOE with age-related macular degeneration–a pooled analysis of 15 studies Decrease in risk associated with each copy of ɛ4 in all age-related macular degeneration sub-phenotypes (Neovascular: OR = 0.74, CI 0.66–0.83; Geographic Atrophic: OR = 0.65, CI 0.55–0.77; Geographic Atrophic Neovascular: OR = 0.71, CI 0.59–0.85; early Age-Related Macular Degeneration: OR = 0.84, CI 0.77–0.92 McKay et al. [71] High
Male and female patients, average age 46, from the dermatology clinic at Hospital Universitario Central Asturias, Spain ɛ3/ɛ4 (N = 54), ɛ4/ɛ4(N = 3), ɛ2/ɛ4(N = 5) Mixed APOE4 allele is associated with psoriasis severity ɛ4 carriers were significantly more common in patients with severe psoriasis compared to controls (p = 0.003) and to non-severe psoriasis (p = 0.017) Coto-Segura et al. [150] Moderate
Children in Brasilia Brazil with and without CP; Age not specified ɛ4 Carriers (N = 139) Mixed Association of APOE genotype and CP Presence of ɛ2 raised the probability of having cerebral palsy (OR 3.2; 95% CI 1.27–8.27). The presence of ɛ4 was not significantly different among groups Braga et al. [73] Moderate
Infants in Edinburgh Scotland ɛ4 Carriers (N = 95) Mixed APOE ɛ4 and its prevalence in early childhood death due to sudden infant death syndrome or to recognized causes Percentage of children with at least one ɛ4 allele was lower in non-SIDS compared to SIDS (p = 0.016) Becher et al. [59] Moderate
Caucasian (70%) and African-American children (30%) from Louisville, KY, area, average age 6.4 years ɛ4 Carriers (N = 19) Mixed APOE ɛ4 allele, cognitive dysfunction, and obstructive sleep apnea in children ɛ4 allele is more frequent in children with obstructive sleep apnea and particularly in children who develop neurocognitive deficits Gozal et al. [151] Low
White, Black, and Hispanic children from the Chicago area; Age not specified ɛ4 Carriers (N = 25 patients; N = 9 controls) Mixed Association of APOE genotype and CP in children Overall risk for CP was elevated 3.4-fold among children carrying an ɛ4 allele Kuroda et al. [75] Low
40 patients with CP and 40 without, in S’ao Paulo, Brazil; Age not specified Total N = 80, 40 with CP, 40 without CP; ɛ4 Carriers (N = 13 patients; N = 4 controls) Mixed Presence of APOE ɛ4 allele in CP OR for correlation between CP and ɛ4 allele = 4.333 de Barros et al. [74] Low

APOE, apolipoprotein E; 95% CI, 95% confidence interval; CP, cerebral palsy; OR, odds ratio; SIDS, sudden infant death syndrome.