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Table 1 Sample demographic and clinical characteristics. The total sample included 465 participants from the National Alzheimer’s Coordinating Uniform Data Set. All participants were diagnosed with normal cognition at the baseline study visit. The final analytic sample included those who remained stable with normal cognition and those who converted to MCI due to AD or AD dementia (n = 56). APOE data were missing for six participants

From: Independent effects of white matter hyperintensities on cognitive, neuropsychiatric, and functional decline: a longitudinal investigation using the National Alzheimer’s Coordinating Center Uniform Data Set

Variable

Mean (SD) or n (%)

Range

Age at baseline MRI visit

68.9 (11.8)

45–100

Total length of follow-up (years)

5.10 (2.14)

1.45–11.67

Total number of follow-up visits

4.62 (1.91)

2–10

Sex

146 (31.4%) male

 

Years of education

15.37 (3.41)

1–25

Ethnicity

86.9% white, 10.3% AA, 2.8% other

 

APOE ε4 carrier status

162 (35.3%) carriers

 

Systolic blood pressure

132 (18.8)

78–198

History of hypertension

200 (43.0%)

 

History of diabetes

80 (17.2%)

 

History of hypercholesterolemia

224 (48.2%)

 

WMH volume at baseline (cm3)

4.70 (8.71)

0–61.24

Natural log of WMH at baseline

0.45 (1.52)

− 2.30–4.12

Diagnosis at final study visit

 Normal cognition

417 (89.7%)

 

 MCI

22 (4.7%)

 

 Dementia

26 (5.6%)

 

CDR Sum of Boxes at final study visit

0.55 (1.83)

0–18

  1. Abbreviations: beta-amyloid, CDR Clinical Dementia Rating scale, MCI mild cognitive impairment, MRI magnetic resonance imaging, WMH white matter hyperintensities