Hyperhomocysteinemia in patients with cardiovascular manifestations: to treat or not to treat

MacFarlane, Amanda J.

doi:10.1093/ajcn/nqab090

Cited by 3 publications

(1 citation statement)

References 9 publications

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“…99 The most common manifestations of deficiencies and inherited metabolic disorders of vitamin B12 and folate are central and peripheral neurological disorders and macrocytic/megaloblastic anemia, with a risk of potentially serious sequelae, which points out the need to properly identify and treat the patients. 100 However, VTE outcomes may be also revealing symptoms of cases with autoimmune gastritis of Addison/Biermer and celiac disease and intermediate/major HHcy. 101 102 103 104 105 Thrombotic outcomes account also among the clinical manifestations of inherited disorders of cobalamin metabolism with a prevalence that dramatically increases with age.…”

Section: Introductionmentioning

confidence: 99%

Hyperhomocysteinemia in Cardiovascular Diseases: Revisiting Observational Studies and Clinical Trials

et al. 2022

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Thromboembolic manifestations are relativement frequent in patients with intermediate/severe hyperhomocysteinemia (> 30 µmol/L) related to inherited disorders and deficiencies in vitamin B12 and folate. In contrast, moderate hyperhomocysteinemia (15- 30 µmol/L) is a modest predictor of cardiovascular risk. The recognition of homocysteine as a cardiovascular risk factor has been challenged by some but not all randomized clinical trials. We reviewed the main data of this controversy and formulated conclusions to be translated in clinical practice. Lowering homocysteine trials have been performed in cardiovascular subjects with moderate but not intermediate/severe hyperhomocysteinemia despite the dose-effect risk association. The first meta-analyses found no benefit and led cardiology societies not recommending homocysteine in the assessment of cardiovascular risk. This guideline challenged the need to diagnose and treat the nutritional and genetic causes of intermediate/major hyperhomocysteinemia and was not revised when larger meta-analyses concluded to a reduced risk of stroke. In a recent observational study, 84% of consecutive cardiovascular patients assessed for homocysteine had intermediate or major hyperhomocysteinemia, which was properly assessed in only half cases and related to B12 and/or folate deficiency and Addisson/Biermer disease in 55% of these cases. In conclusion, revisiting observational studies and clinical trials suggests that cardiovascular patients should be screened for hyperhomocysteinemia, when no other risk factor is found. Patients with intermediate/major hyperhomocysteinemia should be properly assessed and treated for vitamin B deficiencies and inherited disorders according to current guidelines. Further trials are needed to assess the lowering homocysteine effect according to hyperhomocysteinemia categories at baseline.

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