Table 3.
Reference | Study design | Measurement type | Main outcome | |||
---|---|---|---|---|---|---|
Cohort | Size | Follow-up | Mean age | |||
Burnham et al., 2016 [85] | AIBL | N = 573 | 6 years | 73 | Hippocampal volume | Subjects with low hippocampal volume and evidence of amyloid pathology showed faster cognitive decline compared with subjects with normal biomarkers. Subjects with only decreased hippocampal volume in the absence of amyloid pathology did not show significant decline compared to the normal biomarker group |
den Heijer et al., 2010 [83] | Rotterdam study (population-based) | N = 518 | 8 years | 73–79 | Hippocampal atrophy rate | Hippocampal atrophy rates predict cognitive decline in healthy subjects (HR 1.6, 1.2–2.3). |
den Heijer et al., 2006 [82] | Rotterdam study (population-based) | N = 511 | 6 years | 73–79 | Hippocampal volume | Hippocampal volume associated with risk of dementia (HR 3.0, 2.0–4.6). |
Martin et al., 2010 [84] | University of Kentucky AD Centre | N = 71 | 5 years | 78–84 | Hippocampal and subregions volume; entorhinal cortex volume | Greater atrophy in hippocampus (head and body) and entorhinal cortex in subjects converting to MCI. AUC 0.87 for hippocampal head, 0.84 for hippocampal body, 0.79 for entorhinal cortex. |
Stoub et al., 2005 [94] | Rush Alzheimer’s Disease Center (Chicago, USA) | N = 58 (CN and MCI together) | 5 years | 80 | Hippocampal volume and atrophy rates; entorhinal cortex volume and atrophy rates | Baseline entorhinal and slope of decline were predictors for AD. Baseline hippocampal volume and atrophy rates were not (after controlling for entorhinal cortex). |
AD Alzheimer’s disease, AIBL Australian Imaging, Biomarker and Lifestyle study, AUC area under the curve, CN cognitively normal, MCI mild cognitive impairment, HR hazard ratio