TABLE 1.
The demographic information of all samples
Sample no. | Group | Average Agea | Gender (M/F) | Age (y) | Delay of Collection after Death (h) | Weight of Retina (g) | Weight of RPE/Choroid (g) | Eye Disease History | Cause of Death |
---|---|---|---|---|---|---|---|---|---|
1 | Young age group | 16.4 ± 3.6 | M | 17 | 14 | 0.1547 | 0.0953 | No | Heart failure |
2 | F | 22 | 21 | 0.0879 | 0.1208 | No | Respiratory collapse | ||
3 | F | 12 | 16 | 0.1149 | 0.1223 | No | Multiple sclerosis | ||
4 | F | 15 | 22 | 0.0873 | 0.1006 | No | Anoxic brain injury | ||
5 | M | 16 | 22 | 0.1149 | 0.1223 | No | Blunt force head trauma | ||
6 | Middle age group | 38.2 ± 6.2 | M | 36 | 26 | 0.0917 | 0.0867 | No | Respiratory failure |
7 | M | 38 | 26 | 0.0846 | 0.0775 | No | Aspiration pneumonia | ||
8 | M | 49 | 13 | 0.1157 | 0.1181 | No | Respiratory arrest | ||
9 | M | 39 | 16 | 0.1099 | 0.1090 | No | Myocardial infarction | ||
10 | M | 37 | 6 | 0.0799 | 0.0990 | No | End-stage renal failure | ||
11 | M | 30 | 8 | 0.1056 | 0.0976 | No | Congestive heart failure | ||
12 | Old age group | 74.0 ± 3.4 | M | 77 | 15 | 0.1164 | 0.1363 | No | Trauma |
13 | F | 78 | 23 | 0.1332 | 0.0992 | No | Cerebrovascular accident | ||
14 | M | 72 | 20 | 0.1550 | 0.1089 | No | Cerebrovascular accident | ||
15 | F | 70 | 7 | 0.1242 | 0.1378 | No | Cerebrovascular accident | ||
16 | F | 73 | 17 | 0.1542 | 0.1678 | No | Amyotrophic lateral sclerosis | ||
17 | Age-matched AMD group | 77.2 ± 6.4 | M | 78 | 23 | 0.1538 | 0.1375 | AMD | Cancer |
18 | F | 70 | 23 | 0.1123 | 0.1462 | AMD | Myocardial infarction | ||
19 | M | 75 | 22 | 0.1557 | 0.1562 | AMD | Lymphoma | ||
20 | M | 73 | 17 | 0.0947 | 0.1008 | AMD | Respiratory failure | ||
21 | M | 81 | 8 | 0.1357 | 0.1313 | AMDb | Circulatory collapse | ||
22 | F | 84 | 22 | 0.2557 | 0.2562 | AMD | Renal failure | ||
23 | F | 87 | 18 | 0.1671 | 0.1395 | AMDb | Respiratory failure, breast cancer | ||
24 | M | 70 | 8 | 0.1222 | 0.0722 | AMD | Circulatory collapse |
Average ± SD.
These AMD patients had exudative AMD. All other AMD patients had early to intermediate dry AMD with drusen and pigmentary changes but no history of geographic atrophy or exudative disease.