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. 2023 Jun 15;17:1130845. doi: 10.3389/fninf.2023.1130845

Table 1.

Training datasets used for HSF.

Dataset Contrasts Subfields Field Age Condition
Winterburn et al. (2013) T1 and T2 DG/CA/Sub 3T 29–57 -
Kulaga-Yoskovitz et al. (2015) T1 and T2 DG/CA/Sub 3T 21–53 -
Yushkevich et al. (2015b) T1 and T2 DG/CA1/CA2-3/Sub 3T MCI
Hindy et al. (2016) T2 DG/CA1/CA2/CA3/Sub 3T 18–30 -
Bouyeure et al. (2021) T1 and T2 DG/CA1/CA2-3/Sub 3T 4–12 -
Yushkevich et al. (2010) T1 and T2 DG/CA1/CA2/CA3/Sub 4T 38–82 MCI/AD
HIPlay7* T1 and T2 DG/CA1/CA2/CA3/Sub 7T 12–21 TLE
Wisse et al. (2016) T2 DG/CA1/CA2/CA3/Sub 7T 50–68 -
Berron et al. (2017) T1 and T2 DG/CA1/CA2/CA3/Sub 7T 19–32 -
Haeger et al. (2020)** T2 DG/CA1/CA2/CA3/Sub 7T 50–70 -
Shaw et al. (2020)** T1 and T2 DG/CA1/CA2/CA3/Sub 7T 23–29 -
Lagarde et al. (2021)** T2 DG/CA1/CA2/CA3/Sub 7T 50–84 SC/MCI/AD

Description of the training database, alongside their manually segmented hippocampal subfields, namely the dentate gyrus (DG), the cornu ammonis (CA)1, CA2, and CA3. Included participants are either healthy, exhibiting mild cognitive impairments (MCI), Alzheimer's disease (AD), hippocampal sclerosis (SC), or temporal lobe epilepsy (TLE).

*

In-house dataset, ANR-16-NEUC-0001-01; Manual Segmentation on 23 controls and 4 temporal lobe epilepsies; 1 mm T1w and 0.125*0.125*1.2 mm T2w MRIs.

**

Manual segmentations on 7 subjects per dataset performed by the authors (CP, SP, MF, MB, and MN), following Berron et al. (2017).