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. Author manuscript; available in PMC: 2012 Nov 1.
Published in final edited form as: J Mol Neurosci. 2011 May 17;45(3):330–335. doi: 10.1007/s12031-011-9538-y

Table 3.

Studies of survival in FTLD

Location Basis of diagnosis No. of subjects Mean age at diagnosis Delay in diagnosis Survival from onset or diagnosis
Survival from diagnosis
San Francisco (Roberson et al. 2005) Clinical diagnoses 177 58.5+9.4 4.5+2.9 3.6+0.4
San Diego (Rascovsky et al. 2005) Pathologically confirmed 70 65+9.4 4.0+2.8 4.2
Sydney (Garcin et al. 2009) Clinical diagnoses 91 57.2+8.2 (onset) 3.6+2.5 4.2+0.8a
Cambridge and Sydney (Hodges et al. 2003) Pathologically confirmed 61 61.5+7.6 3 3.0+0.4
Survival from onset
Rochester MN (Josephs et al. 2005) Pathologically confirmed 45 57.3+11.1 (onset) 6.6
Philadelphia (Xie et al. 2008) Pathologically confirmed 71 61+9.5 (onset) 1+1 6.6+0.5
Netherlands (Chiu et al. 2010) Clinical diagnoses 354 57.5+8.9 9.9+0.7
a

Cases of “bvFTD phenocopy were excluded” (Davies et al. 2006). If those cases were included, survival from diagnosis was 5.5+4.1