Skip to main content
. Author manuscript; available in PMC: 2023 Sep 1.
Published in final edited form as: Neurobiol Aging. 2022 May 26;117:107–116. doi: 10.1016/j.neurobiolaging.2022.05.007

Table 6.

Association between gender and neuropathological alterations (n = 741).

Small vessel disease
Crude
OR (95% CI)
p Multivariatea
OR (95% CI)
p
No Yes

Female ×
male
311 (88.1%)
347 (90.1%)
42 (11.9%)
38 (9.9%)
0.8 (0.5–1.3) 0.38 0.7 (0.4–1.2) 0.18
Cerebral amyloid angiopathy
No Yes
Female ×
male
336 (95.5%)
375 (97.4%)
16 (4.5%)
10 (2.6%)
0.6 (0.3–1.3) 0.16 0.5 (0.2–1.4) 0.19
Infarcts
No Yes
Female ×
male
325 (92.6%)
359 (93.2%)
26 (7.4%)
26 (6.8%)
0.9 (0.5–1.6) 0.73 1.1 (1.0–2.2) 0.82
Neuritic plaques (beta-amyloid): moderate-frequent
No Yes
Female ×
male
284 (80.2%)
333 (86.0%)
70 (19.8%)
54 (14.0%)
0.7 (0.5–1.0) 0.035 0.7 (0.5–1.2) 0.19
Neurofibrillary pathology (tau) III-VI
No Yes
Female ×
male
234 (66.7%)
291 (76.2%)
117 (33.3%)
91 (23.8%)
0.6 (0.5–0.9) 0.004 0.4 (0.1–1.1) 0.07
Lewy body disease
No Yes
Female ×
male
307 (90.3%)
338 (90.6%)
33 (9.7%)
35 (9.4%)
1.0 (0.6–1.6) 0.88 1.0 (0.6–1.9) 0.89

Key: a-MDD, adult-onset major depressive disorder; 95% CI, 95% Confidence Interval; DS, depressive symptoms 3 months prior to death; LLD, late life MDD; MDD, major depressive disorder.

a

Logistic regression models adjusted for age at death, education, alcohol misuse, smoking, and hypertension.