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. 2014 Jun 4;2(5):430–437. doi: 10.1002/mgg3.85

Table 1.

Demographic and clinical characteristics of sequenced participants and family members

Sequenced Relatives Controls



Characteristics n Mean n Mean n Mean
Number of subjects sequenced/genotyped1 195 318 498
Number of families2 194 56
Affection status
 Affected 183 94.0% 104 33.0%
 Unaffected 10 5.0% 197 62.0% 498 100.0%
 Unknown 2 1.0% 17 5.0%
Proportion of females 64/131 67.2% 142/176 55.30% 152/346 69.5
Age (year)
 Age at onset of affected 56.9 (SD = 7.29) 68.5 (SD = 12.64)
 Age at last examination of unaffected 66.7 (SD = 5.66) 58.8 (SD = 11.31) 79.1 (SD= 6.2)
 Range of age at onset 40–73 44–98
Education (year) 8.4 (SD = 5.45) 90 (SD =5.79 ) 7.6 (SD = 4.35)
 Range of education 0–20 0–22 0–20
Residency
 Puerto Rico 67 34.4% 147 46.2% 69 13.9%
 Dominican Republic 127 65.1% 165 51.9% 210 42.2%
 USA 1 0.5% 0 0.0% 10 2.0%
 Other Hispanics3 0 0.0% 0 0.0% 132 26.5%
 Unknown/others4 0 0.0% 6 1.9% 77 15.5%
APOE allele frequencies
E4 32.1% 24.1% 13.0%
E3 64.4% 70.9% 79.2%
E2 3.6% 5.0% 7.8%
1

Three individuals identified from separate sequencing experiments.

2

One family had more than one person sequenced.

3

Self-reported Hispanics but unclear about their nationality and place of birth.

4

Incomplete information.