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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Direct observations: clinical cases, poisoning incidents and other

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Administrative data

Endpoint:
direct observations: clinical cases, poisoning incidents and other
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Case report.

Data source

Reference
Reference Type:
publication
Title:
Adverse event associated with methionine loading test: a case report.
Author:
Cottington EM, LaMantia C, Stabler SP, Allen RH, Tangerman A, Wagner C, Zeisel SH, Mudd SH
Year:
2002
Bibliographic source:
Arterioscler Thromb Vasc Biol. 2002 Jun 1;22(6):1046-50.

Materials and methods

Study type:
clinical case study
Principles of method if other than guideline:
Case report regarding the death of a 69-year-old African American woman who was recruited and consented to participate in a study of methionine-homocysteine metabolism and its relationship to Alzheimer’s disease.

Test material

Constituent 1
Chemical structure
Reference substance name:
L-methionine
EC Number:
200-562-9
EC Name:
L-methionine
Cas Number:
63-68-3
Molecular formula:
C5H11NO2S
IUPAC Name:
L-methionine

Method

Subjects:
- Number of subjects exposed:
- Sex:female
- Age: 69 yeras
- Race: African American woman
Route of exposure:
oral
Reason of exposure:
intentional
Details on exposure:
intended dose: 100 mg/kg bw
Although there was no direct evidence that the dose of methionine received was incorrect, the blood analysis data are consistant with a dose approximately 10 times what was intended.

Results and discussion

Any other information on results incl. tables

After 2 h 40 min after the loading dose, the volunteer began to vomit and continued for several hours, during which prochlorperazine and diphenhydramine were given. At about 8 h after the methionine was given, she was taken to the emergency room, subsequently became apneic and pulseless, and was admitted to an intensive care unit. After various other complications, she died 30 d after the methionine load was administered. Retrospective measurements of plasma methionine showed it to be about 200 times the baseline value at 2 h after the dose, even higher at 4 h, and 10 times the baseline value after 2 d. Although there was no direct evidence that the dose of methionine was incorrect, the blood analysis data are consistent with a dose approximately 10 times what was intended (i.e.,70 times the dietary requirement).

Applicant's summary and conclusion