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. 2010 Aug 6;5(8):e12037. doi: 10.1371/journal.pone.0012037

Table 2. Frequencies of mtDNA sub-haplogroups in AD patients and controls from Italy.

Sub-haplogroupa AD patients Controls
(N = 936) (N = 776)
N % SEb N % SEb
H* 182 19,4 0,0129 156 20,1 0,0144
H1 115 12,3 0,0107 97 12,5 0,0119
H3 28 3,0 0,0056 18 2,3 0,0054
H5c 39 4,2 0,0065 18 2,3 0,0054
H6 33 3,5 0,0060 21 2,7 0,0058
J1 64 6,8 0,0082 49 6,3 0,0087
J2 14 1,5 0,0040 13 1,7 0,0046
R0 46 4,9 0,0071 46 5,9 0,0085
T1 21 2,2 0,0048 17 2,2 0,0053
T2 84 9,0 0,0093 70 9,0 0,0103
U* 38 4,1 0,0065 32 4,1 0,0071
K 67 7,2 0,0084 68 8,8 0,0102
U4 23 2,5 0,0051 16 2,1 0,0051
U5a 46 4,9 0,0071 38 4,9 0,0077
U5b 18 1,9 0,0045 22 2,8 0,0060
V 31 3,3 0,0058 29 3,7 0,0068
W 20 2,1 0,0047 16 2,1 0,0051
X 26 2,8 0,0054 15 1,9 0,0049
Other 41 4,4 0,0067 35 4,5 0,0074
a

Sub-haplogroups with frequencies lower than 1.5% were grouped. Thus R0 includes R0a, R1, HV*, HV0*, HV0a, HV1 and HV2; H* includes all mtDNAs belonging to haplogroup H, except those further classified (H1, H3, H5 and H6); the same rationale has been used for U*; whereas “Other” contains the heterogeneous haplogroups I, L1b, L2a, L2c, L3d, L3e, M, N and N1.

b

Standard Error.

c

Only for H5 there is a difference between AD patients and controls with a χ2 p-value (not adjusted for multiple comparisons) of 0.034.