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. Author manuscript; available in PMC: 2024 Feb 12.
Published in final edited form as: J Alzheimers Dis. 2023;93(3):949–961. doi: 10.3233/JAD-221224

Table 5.

Risk of select neuropathological endpoints among those with baseline TBI with LOC a ≤1 hour or >1 hour at baseline, compared to those with no TBI with LOC at baseline.

Hour or less (n = 126) Over an hour (n = 19)

Neuropath outcomeb N RRc (95% CI) p RRc (95% CI) p

Braak stage V or VI 750 1.01 (0.74, 1.36) 0.96 1.12 (0.49, 2.04) 0.77
LATE stage >0 751 1.00 (0.75, 1.31) 0.99 1.01 (0.52, 1.64) 0.97
Any cerebral or deep microvascular lesions 749 0.97 (0.73, 1.27) 0.81 1.20 (0.55, 1.96) 0.53
Any cerebral microvascular lesions 749 0.92 (0.66, 1.28) 0.65 1.06 (0.45, 2.00) 0.88
Any deep microvascular lesions 749 0.87 (0.58, 1.31) 0.53 1.58 (0.66, 2.90) 0.21
Any Macroinfarcts 771 1.04 (0.70, 1.51) 0.83 0.97 (0.37, 1.94) 0.94
Ratio of fixed brain weight to expected weightd 621 1.00 (0.97, 1.02) 0.96 0.99 (0.93, 1.06) 0.88
Centimeters of cerebral cortical atrophye 669 1.16 (0.94, 1.43) 0.16 1.53 (0.86, 2.80) 0.17
a

At least one report of TBI with LOC as of ACT study entry, based on ACT study data, or, when available, on BISQ self-report or proxy or chart review.

b

Some outcomes were too rare to assess by LOC duration.

c

Adjusted rate ratios (RR) and 95% confidence intervals (CI) are from Poisson regressions modified with robust standard errors, adjusting for age at death, sex, education, any Apoe4 alleles, TBI with LOC after baseline, and ACT study cohort. Results were weighted back to the full cohort in a bootstrapping procedure that accounted for the error in estimating the weights, resulting in wider confidence intervals and higher p-values than in unweighted results.

d

Total fixed brain weight divided by the expected brain weight, where the expected brain weight was calculated as 200 + the posterior fossa contents weight/0.15.

e

Atrophy defined by dilatation in the lateral ventricles at the level of the temporal tip.