Durso · Journal of clinical pharmacology 2000 · non-randomized pharmacokinetic study · n=9

Variable absorption of carbidopa affects both peripheral and central levodopa metabolism.

Cited 30 times in the scientific literature.

Level 4 - case-series / case-control

Small single-arm pharmacokinetic study without a separate control group

PubMed 10934669 · doi:10.1177/00912700022009585 · record verified 2026-08-30

What was done

Nine patients with Parkinson disease were given 50 mg oral carbidopa followed 1 hour later by an intravenous infusion of 150 mg stable isotope-labeled levodopa. Eight patients underwent lumbar puncture at 6 hours post-infusion. Blood and cerebrospinal fluid (CSF) samples were analyzed by high-performance liquid chromatography and mass spectrometry. Participants were divided post hoc into slow and rapid carbidopa absorption groups.

What was found

Poor carbidopa absorbers had significantly greater peripheral levodopa decarboxylation measured by serum-labeled HVA AUC (p = 0.05). Elimination half-lives of serum levodopa did not differ between groups. Serum carbidopa AUC correlated with percent-labeled HVA in CSF (R = 0.786, p = 0.02). Rapid absorbers had higher percent-labeled CSF HVA compared to slow absorbers (60% vs. 49%, p = 0.02).

Why it matters

This indicates that standard clinical doses of carbidopa do not saturate peripheral aromatic L-amino acid decarboxylase, meaning variations in carbidopa absorption can alter central dopamine availability.

Limits

The sample size is very small (n=9 total, n=8 with CSF data). The split into absorption categories was non-randomized and observational, and clinical Parkinsonian motor outcomes were not assessed.

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