Penn Frontotemporal Degeneration Center, Department of Neurology, School of Medicine, University of Pennsylvania, Philadelphia.
Department of Family and Community Health, School of Nursing, University of Pennsylvania, Philadelphia.
JAMA Neurol. 2023 Nov 1;80(11):1191-1198. doi: 10.1001/jamaneurol.2023.3093.
Prior research suggests there are racial disparities in the presentation of dementia, but this has not been investigated in the context of frontotemporal dementia (FTD).
To explore racial disparities in dementia severity, functional impairment, and neuropsychiatric symptoms in individuals with a diagnosis of FTD.
DESIGN, SETTING, AND PARTICIPANTS: This exploratory cross-sectional study of National Alzheimer's Coordinating Center (NACC) data collected between June 2005 to August 2021 evaluated Asian, Black, and White individuals with a diagnosis of FTD (behavioral variant FTD or primary progressive aphasia). Excluded were races with limited data, including American Indian or Alaska Native (n = 4), Native Hawaiian or other Pacific Islander (n = 3), other (n = 13), and unknown (n = 24), and participants with symptom duration more than 4 SDs above the mean.
Racial differences at initial NACC visit were examined on Clinical Dementia Rating Dementia Staging Instrument plus NACC Frontotemporal Lobar Degeneration Behavior & Language Domains (FTLD-CDR), Functional Assessment Scale, and Neuropsychiatric Inventory using regression models. Matching was also performed to address the imbalance between racial groups.
The final sample comprised 2478 individuals, of which 59 (2.4%) were Asian, 63 (2.5%) were Black, and 2356 (95.1%) were White. The mean (SD) age at initial visit was 65.3 (9.4) years and symptom duration at initial visit was 67.5 (35.6) months. Asian and Black individuals were considerably underrepresented, comprising a small percent of the sample. Black individuals had a higher degree of dementia severity on FTLD-CDR (β = 0.64; SE = 0.24; P = .006) and FTLD-CDR sum of boxes (β = 1.21; SE = 0.57; P = .03) and greater functional impairment (β = 3.83; SE = 1.49; P = .01). There were no differences on FTLD-CDR and Functional Assessment Scale between Asian and White individuals. Black individuals were found to exhibit a higher frequency of delusions, agitation, and depression (delusions: odds ratio [OR], 2.18; 95% CI, 1.15-3.93; P = .01; agitation: OR, 1.73; 95% CI, 1.03-2.93; P = .04; depression: OR, 1.75; 95% CI, 1.05-2.92; P = .03). Asian individuals were found to exhibit a higher frequency of apathy (OR, 1.89; 95% CI, 1.09-3.78; P = .03), nighttime behaviors (OR, 1.72; 95% CI, 1.01-2.91; P = .04), and appetite/eating (OR, 1.99; 95% CI, 1.17-3.47; P = .01) compared to White individuals.
This exploratory study suggests there are racial disparities in dementia severity, functional impairment, and neuropsychiatric symptoms. Future work must address racial disparities and their underlying determinants as well as the lack of representation of racially minoritized individuals in nationally representative dementia registries.
先前的研究表明,痴呆症在表现上存在种族差异,但这在额颞叶痴呆(FTD)的背景下尚未得到研究。
探讨在 FTD 诊断个体中,痴呆严重程度、功能障碍和神经精神症状的种族差异。
设计、地点和参与者:本研究为国家阿尔茨海默病协调中心(NACC)数据的探索性横断面研究,数据收集时间为 2005 年 6 月至 2021 年 8 月,评估了亚洲、黑人和白人的 FTD(行为变异型 FTD 或原发性进行性失语症)患者。排除了种族数据有限的种族,包括美洲印第安人或阿拉斯加原住民(n=4)、夏威夷原住民或其他太平洋岛民(n=3)、其他(n=13)和未知(n=24),以及症状持续时间超过平均 4 个标准差的参与者。
使用回归模型,在初始 NACC 就诊时,根据临床痴呆评定痴呆分期量表加 NACC 额颞叶变性行为和语言域(FTLD-CDR)、功能评估量表和神经精神疾病量表,检查了种族差异。还进行了匹配,以解决种族群体之间的不平衡。
最终样本包括 2478 人,其中 59 人(2.4%)为亚洲人,63 人(2.5%)为黑人,2356 人(95.1%)为白人。初始就诊时的平均(SD)年龄为 65.3(9.4)岁,初始就诊时的症状持续时间为 67.5(35.6)个月。亚洲人和黑人的人数严重不足,占样本的一小部分。黑人在 FTLD-CDR 上的痴呆严重程度(β=0.64;SE=0.24;P=0.006)和 FTLD-CDR 总分(β=1.21;SE=0.57;P=0.03)以及更大的功能障碍上存在较大差异(β=3.83;SE=1.49;P=0.01)。亚洲人和白人在 FTLD-CDR 和功能评估量表上没有差异。发现黑人更频繁地出现妄想、激越和抑郁(妄想:比值比[OR],2.18;95%置信区间[CI],1.15-3.93;P=0.01;激越:OR,1.73;95%CI,1.03-2.93;P=0.04;抑郁:OR,1.75;95%CI,1.05-2.92;P=0.03)。与白人相比,发现亚洲人更容易出现冷漠(OR,1.89;95%CI,1.09-3.78;P=0.03)、夜间行为(OR,1.72;95%CI,1.01-2.91;P=0.04)和食欲/进食(OR,1.99;95%CI,1.17-3.47;P=0.01)。
这项探索性研究表明,痴呆严重程度、功能障碍和神经精神症状存在种族差异。未来的工作必须解决种族差异及其潜在决定因素,以及在全国代表性的痴呆登记处中代表性不足的少数族裔个体的缺乏。