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J-Editing Proton MR Spectroscopy for Brain Signal Separation in Methylmalonic Acidemia: A Pediatric Case-Control
Mengyuan Zhuo1, Yan Yun2, Jiaxiang Xin3
1Department of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, No. 324 JingWu Rd, Jinan 250021, China.
Abstract:
Background Methylmalonic acid (MMA) accumulates due to mitochondrial dysfunction or enzymatic deficiencies. Methylmalonic acidemia causes central nervous system damage. In vivo detection of MMA using conventional proton (1H) MR spectroscopy is hindered by overlap with lactate and lipids at 1.33 ppm. Purpose To evaluate the feasibility of an optimized J-editing 1H MR spectroscopy protocol to selectively detect MMA and lactate signals in both phantoms and individuals with methylmalonic acidemia. Materials and Methods In this prospective pediatric case-control study, individuals with genetically confirmed methylmalonic acidemia and age-matched control participants underwent brain J-editing 1H MR spectroscopy. The primary endpoint was the feasibility of selective in vivo detection of cerebral MMA using J-editing 1H MR spectroscopy. Phantoms were prepared with different MMA to lactate ratios. Correlations between cerebral MMA signals and biochemical markers (blood propionylcarnitine to acetylcarnitine [C3/C2] ratio and urinary MMA levels) were assessed using Spearman correlation in individuals diagnosed with methylmalonic acidemia. The diagnostic performance of MR spectroscopy and urinary MMA measurement was evaluated against genetic confirmation with use of sensitivity, specificity, and receiver operating characteristic curves. Results A total of 42 participants were included: 24 with methylmalonic acidemia (mean age, 8.7 years ± 5.2 [SD]) and 18 control participants (mean age, 8.9 years ± 4.0 [SD]). The J-editing 1H MR spectroscopy protocol effectively separated MMA and lactate signals in the brains of individuals with methylmalonic acidemia, consistent with phantom results. No abnormal MMA peaks were observed in control participants. The intensity of cerebral MMA signals correlated with blood C3/C2 ratio (Spearman ρ = 0.53 [95% CI: 0.15, 0.78]; P = .008) and urinary MMA levels (ρ = 0.66 [95% CI: 0.33, 0.84]; P < .001). Conclusion J-editing 1H MR spectroscopy reliably and noninvasively detected cerebral MMA in vivo, distinguishing it from overlapping lactate signals. © RSNA, 2026 Supplemental material is available for this article.
Insights
Optimized J-editing 1H MR spectroscopy noninvasively detects cerebral methylmalonic acid (MMA) in vivo, overcoming signal overlap issues. This method aids in diagnosing methylmalonic acidemia by distinguishing MMA from lactate signals.
Area of Science:
- Biomedical Engineering
- Neuroimaging
- Metabolic Disorders
Background:
- Methylmalonic acid (MMA) accumulation from mitochondrial dysfunction or enzyme deficiencies can cause central nervous system damage.
- In vivo detection of MMA via conventional proton (1H) MR spectroscopy is challenging due to signal overlap with lactate and lipids.
- Methylmalonic acidemia requires accurate diagnostic methods for timely intervention.
Purpose of the Study:
- To assess the feasibility of an optimized J-editing 1H MR spectroscopy protocol for selective MMA and lactate detection.
- To evaluate the protocol's efficacy in phantoms and in pediatric patients with methylmalonic acidemia.
- To correlate in vivo MMA signals with established biochemical markers.
Main Methods:
- A prospective pediatric case-control study involving 24 patients with methylmalonic acidemia and 18 controls.
- Brain J-editing 1H MR spectroscopy was performed on all participants.
- Phantoms with varying MMA to lactate ratios were used; correlations with blood C3/C2 ratio and urinary MMA levels were analyzed.
Main Results:
- The J-editing 1H MR spectroscopy protocol successfully differentiated MMA and lactate signals in patients' brains.
- No abnormal MMA peaks were detected in control participants.
- Cerebral MMA signal intensity showed significant correlation with blood C3/C2 ratio (ρ = 0.53, P = .008) and urinary MMA levels (ρ = 0.66, P < .001).
Conclusions:
- J-editing 1H MR spectroscopy provides a reliable, noninvasive method for in vivo detection of cerebral MMA.
- This technique effectively distinguishes MMA from overlapping lactate signals, improving diagnostic capabilities for methylmalonic acidemia.
- The study validates the use of this advanced MR spectroscopy technique in clinical settings for metabolic disorder diagnosis.
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