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. 2020 Oct 22;7:578640. doi: 10.3389/fmolb.2020.578640

TABLE 2.

Effect of diagnosis, age and diagnosis x age interaction on mitochondrial outcomes evaluated in controls, PM and FXTAS female carriers.

Diagnosis x age interaction Diagnosis effect Age effect
Controls vs. PM
ROS (DFn = 1, DFd = 26) F = 1.05e-003 F = 1.45 F = 0.01
p = 0.9744 p = 0.2396 p = 0.9133
CS (DFn = 1, DFd = 24) F = 0.57 F = 4.84 F = 6.83
p = 0.4560 p = 0.0377 p = 0.0153
M/G (DFn = 1, DFd = 26) F = 0.07 F = 4.75 F = 0.46
p = 0.7989 p = 0.0385 p = 0.5019
S (DFn = 1, DFd = 25) F = 0.21 F = 4.80 F = 0.08
p = 0.6542 p = 0.0381 p = 0.7863
αGP (DFn = 1, DFd = 26) F = 0.04 F = 8.08 F = 0.09
p = 0.8433 p = 0.0086 p = 0.7623
CCO (DFn = 1, DFd = 26) F = 1.8e-003 F = 6.82 F = 0.02
p = 0.9665 p = 0.0148 p = 0.9026
Basal (DFn = 1, DFd = 27) F = 0.01 F = 5.94 F = 4.16e-005
p = 0.9362 p = 0.0217 p = 0.9949
Coupling (DFn = 1, DFd = 26) F = 0.08 F = 1.23 F = 1.23
p = 0.7832 p = 0.2760 p = 0.4929
PM vs. FXTAS
ROS (DFn = 1, DFd = 35) F = 0.36 F = 9.36 F = 0.42
p = 0.5537 p = 0.0042 p = 0.5230
CS (DFn = 1, DFd = 41) F = 2.20 F = 0.50 F = 1.67
p = 0.1461 p = 0.4839 p = 0.2029
M/G (DFn = 1, DFd = 40) F = 2.42 F = 0.28 F = 1.89
p = 0.1279 p = 0.5971 p = 0.1766
S (DFn = 1, DFd = 39) F = 1.24e-004 F = 3.48 F = 0.05
p = 0.9912 p = 0.0697 p = 0.8193
αGP (DFn = 1, DFd = 39) F = 0.09 F = 0.11 F = 0.11
p = 0.7604 p = 0.7376 p = 0.7408
CCO (DFn = 1, DFd = 41) F = 0.55 F = 2.54 F = 0.26
p = 0.4632 p = 0.1189 p = 0.6161
Basal (DFn = 1, DFd = 40) F = 0.40 F = 0.65 F = 0.55
p = 0.5296 p = 0.4242 p < 0.4632
Coupling (DFn = 1, DFd = 40) F = 1.71e-003 F = 5.00 F = 0.14
p = 0.9672 p = 0.0312 p = 0.7118

αGP, alpha-glycerophosphate; Basal, glucose-sustained mitochondrial ATP production; CCO, cytochrome c oxidase; CS, citrate synthase activity; M/G, malate/glutamate; ROS, reactive oxygen species; S, succinate. DF, degrees of freedom; DFn, number of groups -1; DFd, number of subjects – DFn. Numerosity of the groups is as follows. For the comparison between controls and PM: younger controls, n = 4; older controls n = 4; younger PM, n = 7, older PM, n = 13. For the comparison between younger and older carriers: younger PM, n = 17; older PM, n = 5; younger FXTAS, n = 5; older FXTAS, n = 15). Note: in some instances, outcomes for 1–6 samples were not tested for lack of biological material. Bolded are statistically significant p values (<0.05).