Evidence map›Paper›PMID 27246648›Full record

ArticleNeurotoxicology2017

Lower sulfurtransferase detoxification rates of cyanide in konzo-A tropical spastic paralysis linked to cassava cyanogenic poisoning.

K J Kambale, E R Ali, N H Sadiki, K P Kayembe, L G Mvumbi, D L Yandju, M J Boivin, G R Boss, D D Stadler, W E Lambert and 5 more

Abstract read
In one paragraph

Article in Neurotoxicology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Motor control and cognition deficits associated with protein carbamoylation in food (cassava) cyanogenic poisoning: Neurodegeneration and genomic perspectives.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2021
    Article
  3. Review
  4. Article
  5. Article
  6. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 2 countries.

K J KambaleDepartment of Biomedical Sciences, University of Kinshasa, Congo-Kinshasa, Democratic Republic of the Congo.
E R AliDepartment of Biology, University of Kinshasa, Congo-Kinshasa, Democratic Republic of the Congo; Institut National de Recherches Biomédicales (INRB), Congo-Kinshasa, Democratic Republic of the Congo.
N H SadikiSchool of Public Health, University of Kinshasa, Congo-Kinshasa, Democratic Republic of the Congo.
K P KayembeSchool of Public Health, University of Kinshasa, Congo-Kinshasa, Democratic Republic of the Congo.
L G MvumbiDepartment of Biomedical Sciences, University of Kinshasa, Congo-Kinshasa, Democratic Republic of the Congo.
D L YandjuDepartment of Biology, University of Kinshasa, Congo-Kinshasa, Democratic Republic of the Congo.
M J BoivinDepartment of Psychiatry and Neurology/Ophthalmology, Michigan State University, East Lansing, MI, USA.
G R BossDepartment of Medicine, University of California, San Diego, La Jolla, CA, USA.
D D StadlerGraduate Programs in Human Nutrition, Oregon Health & Science University, Portland, OR, USA.
W E LambertDepartment of Public Health and Preventive Medicine, Oregon Health & Science University, Portland, OR, USA.
M R LasarevDepartment of Public Health and Preventive Medicine, Oregon Health & Science University, Portland, OR, USA; Oregon Institute of Occupational Health Sciences, Oregon Health & Science University, Portland, OR, USA.
L A OkitunduDepartment of Neurology, University of Kinshasa, Congo-Kinshasa, Democratic Republic of the Congo.
D Mumba NgoyiDepartment of Tropical Medicine, University of Kinshasa, Congo-Kinshasa, Democratic Republic of the Congo; Institut National de Recherches Biomédicales (INRB), Congo-Kinshasa, Democratic Republic of the Congo.
J P BaneaSchool of Public Health, University of Kinshasa, Congo-Kinshasa, Democratic Republic of the Congo; National Nutrition Program, Ministry of Health, Congo-Kinshasa, Democratic Republic of the Congo.
D D Tshala-KatumbayDepartment of Neurology, University of Kinshasa, Congo-Kinshasa, Democratic Republic of the Congo; Institut National de Recherches Biomédicales (INRB), Congo-Kinshasa, Democratic Republic of the Congo; Department of Neurology, Oregon Health & Science University, Portland, OR, USA. Electronic address: tshalad@ohsu.edu.
University of Kinshasa · CDOregon Health & Science University · USNational Institute of Biomedical Research · CDMichigan State University · USUniversity of California, San Diego · US

Funding

Pre-Clinical and Clinical Studies of Cobinamide, A New Cyanide Detoxifying AgentU01NS058030 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BOSS, GERRY R · 2006 to 2017
$7.3M
Toxicodietary and genetic determinants of susceptibility to neurodegenerationR01ES019841 · NIEHS · OREGON HEALTH & SCIENCE UNIVERSITY · PI TSHALA-KATUMBAY, DANIEL DESIRE · 2011 to 2020
$4.6M
Food(cassava) cyanogen exposure and motor neuron degenerationR21ES017225 · NIEHS · OREGON HEALTH & SCIENCE UNIVERSITY · PI TSHALA-KATUMBAY, DANIEL DESIRE · 2009 to 2010
$338k
NIEHS NIH HHS R01 ES019841NIEHS NIH HHS R21 ES017225NINDS NIH HHS U01 NS058030
6 · The paper itself

Abstract

Using a matched case-control design, we sought to determine whether the odds of konzo, a distinct spastic paraparesis associated with food (cassava) cyanogenic exposure in the tropics, were associated with lower cyanide detoxification rates (CDR) and malnutrition. Children with konzo (N=122, 5-17 years of age) were age- and sex-matched with presumably healthy controls (N=87) and assessed for motor and cognition performances, cyanogenic exposure, nutritional status, and cyanide detoxification rates (CDR). Cyanogenic exposure was ascertained by thiocyanate (SCN) concentrations in plasma (P-SCN) and urine (U-SCN). Children with a height-for-age z-score (HAZNCHS)<-2 were classified as nutritionally stunted. CDR was measured as time required to convert cyanide to SCN, and expressed as ms/μmol SCN/mg protein or as mmolSCN/ml plasma/min. Mean (SD) U-SCN in children with konzo was 521.9 (353.6) μmol/l and was, significantly higher than 384.6 (223.7) μmol/l in those without konzo. Conditional regression analysis of data for age- and sex- matched case-control pairs showed that konzo was associated with stunting (OR: 5.8; 95% CI: 2.7-12.8; p<0.01; N=83 paired groups) and higher U-SCN (OR: 1.1; 95% CI: 1.02-1.20 per 50-μmol increase in U-SCN; p=0.02; N=47 paired groups). After adjusting for stunting and U-SCN, the odds of developing konzo was reduced by 63% (95% CI: 11-85%, p=0.03; N=41 paired groups) for each 5mmol SCN/(ml plasma/min)-increase in CDR. Linear regression analysis indicated a significant association between BOT-2 or KABC-II scores and both the HAZNCHS z-score and the U-SCN concentration, but not the CDR. Our findings provide evidence in support of interventions to remove cyanogenic compounds from cassava prior to human consumption or, peharps, enhance the detoxification of cyanide in those relying on the cassava as the main source of food.

Indexed as

AdolescentAnalysis of VarianceCase-Control StudiesChildChild, PreschoolCognition DisordersCyanidesFemaleHumansMaleMotor DisordersNitrilesParaparesis, Tropical SpasticRetrospective StudiesStatistics, NonparametricSulfurtransferasesCyanidescyanogenNitrilesSulfurtransferasesCassavaCyanide detoxificationKonzoNeurotoxicityRhodaneseSulfurtransferases

Identifiers

PMID27246648
PMCPMC5125906
OpenAlexW2412779404

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.