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Facts and Recommendations about Total Homocysteine Determinations: An Expert Opinion

Clinical Chemistry · 2004 · Vol. 50(1) · pp. 3–32
Helga RefsumA. David SmithPer Magne UelandEbba NexøRobert ClarkeJoseph McPartlinCarole JohnstonF EngbaekJørn SchneedeCatherine McPartlinJohn M. Scott

Abstract

This review is divided into two sections: (a) determination of homocysteine (methods and their performance, sample collection and handling, biological determinants, reference intervals, within-person variability, and methionine loading test); and (b) risk assessment and disease diagnosis (homocystinuria, folate and cobalamin deficiencies, cardiovascular disease, renal failure, psychiatric disorders and cognitive impairment, pregnancy complications and birth defects, and screening of elderly and newborns). Each of these subsections concludes with a separate series of recommendations to assist the clinician and the research scientist in making informed decisions. The review concludes with a list of unresolved questions.

Folate and B Vitamins ResearchEsophageal and GI PathologyMetabolism and Genetic DisordersHomocysteineExpert opinionHomocystinuriaMedicineCobalaminDiseaseMEDLINECognitive impairmentClinical significanceIntensive care medicine

MeSH terms

Blood Specimen CollectionHomocysteineHumansMass ScreeningReference ValuesRisk AssessmentEvidence-Based MedicineClinical Laboratory Techniques

Funding

  • U.S. Department of Agriculture
  • University of Oxford
  • Universitetet i Bergen
  • Medical Research Council
Citations
1,046
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42.57
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