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. 2022 Dec 13;13:1090958. doi: 10.3389/fneur.2022.1090958

Table 2.

Metabolite analysis in the participants.

Control HHcy cblC-MMA
methylmalonic acid in urine (mmol/mmol creatinine) 0.00 (0.00–0.00) 0.00 (0.00–0.00) 0.74 (0.58–1.14)*&
HCY in serum (μmol/L) 5.44 (4.65–5.78) 89.70 (69.74–112.49) * 156.68 (150.07–171.08)*&
methylmalonic acid in serum (μmol/L) 0.05 (0.04–0.08) 0.06 (0.04–0.12) 5.73 (4.36–7.20)*&
C3 (μmol/L) 3.85 (3.10–4.34) 4.82 (3.48–7.06) * 7.28 (4.87–9.11)*
C0 (μmol/L) 27.4 (25.3–30.5) 25.3 (21.4–28.3) 17.60 (13.9–23.3)*&
C3/C0 0.14 (0.11–0.15) 0.22 (0.14–0.32) * 0.36 (0.25–0.56)*
*

p < 0.01 compared with control group;

&

p < 0.05 compared with HHcy group; HHcy, non-inherited hyperhomocysteinemia; MMA, methylmalonic acidemia; HCY, homocysteine; C3, propionylcarnitine; C0, free carnitine; C3/C0, the ratio of C3 and C0. Data were shown as median with 95% CI.