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. 2013 Sep 18;7(5):383–393. doi: 10.4161/pri.26416

Table 2. Cases studied in the present series.

Western blot
  Frontal cortex Cerebellum
  Control (n = 15) MM1 sCJD (n = 15) VV2 sCJD (n = 15) Control (n = 15) MM1 sCJD (n = 15) VV2 sCJD (n = 14)
Gender (M/F) 10/5 10/5 5/10 11/4 10/5 4/10
Age (years)* 60(15) 68(9) 61(11) 62(12) 66(15) 63(11)
RT-qPCR
  Frontal cortex Cerebellum
  Control (n = 15) MM1 sCJD (n = 15) VV2 sCJD (n = 15) Control (n = 15) MM1 sCJD (n = 15) VV2 sCJD (n = 10)
Gender (M/F) 10/5 10/5 5/10 10/5 10/5 4/6
Age (years)* 60(16) 64(14) 63(11) 63(12) 66(15) 63(11)
  Western blot RT-qPCR
  Control (n = 14) AD (n = 14) LBD (n = 14) Control (n = 15) AD (n = 29) LBD (n = 20)
Gender (M/F) 9/5 7/7 10/4 6/9 13/16 12/8
Age (years)* 69(12) 74(6) 71(10) 70(12) 78(7) 72(11)
  Control (n = 7) PSP (n = 10) FTLD (n = 10) Control (n = 15) PSP (n = 10) FTLD (n = 10)
Gender (M/F) 4/3 4/6 4/6 9/6 4/6 4/6
Age (years)* 71(9) 73(6) 68(7) 72(11) 73(6) 68(7)

*Mean (SD). Control refers to cases with no neuropathological changes and cases with a few neurofibrillary tangles in the entorhinal and transentorhinal cortex (Braak stages I-II) if older than 62 y. sCJD, sporadic Creutzfeldt-Jakob disease (MM1 and VV2 subtypes); AD III-VI, Alzheimer disease stages III-VI according to Braak and Braak; LBD, Lewy body disease stages 3–6 of Braak; PSP, progressive supranuclear palsy; FTLD, frontotemporal lobar degeneration. FTLD included familial FTLD-tau due to mutations in the tau gene(fFTLD-tau) and FTLD-TDP-43 cases.

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