Additional file 2 of Neurodegenerative pathologies associated with behavioral and psychological symptoms of dementia in a community-based autopsy cohort

Additional file 2: Table S2. Average raw numbers of different BPSD subtypes per individual participant by pathology category. Table S3. Sample sizes of subsets of cases, stratified by pathological features. Table S4. Odds ratio (and 95% CI) of having any degree of BPSD (scored 1, 2, or 3 versus none), stratified by pathology, in cases with Braak NFT stage < V and relatively pure subtypes of pathology; analogous to Table 5. Table S5. Odds ratio (and 95% CI) of having any degree of BPSD (scored 1, 2, or 3 versus none), stratified by pathology, in cases with Braak NFT stages V or VI; analogous to Table 6. Table S6. p values for radar charts (Figs. 2, 3, 4), stratified by BPSD subtypes.

附加文件2：表S2。按病理类别划分的每名受试者不同行为与精神症状（Behavioral and Psychological Symptoms of Dementia, BPSD）亚型的原始平均计数。
表S3：按病理特征分层的病例亚组样本量。
表S4：在Braak神经原纤维缠结（Neurofibrillary Tangles, NFT）分期低于V期且病理类型相对单纯的病例中，按病理特征分层的任意程度BPSD（评分为1、2或3分与无该症状）的比值比（及95%置信区间），与表5类似。
表S5：在Braak NFT分期为V期或VI期的病例中，按病理特征分层的任意程度BPSD（评分为1、2或3分与无该症状）的比值比（及95%置信区间），与表6类似。
表S6：按BPSD亚型分层的雷达图（图2、3、4）对应的p值。