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Elevated plasma homocysteine levels in patients with amyotrophic lateral sclerosis.
Neurology. 2008 Jan 15; 70(3):222-5.Neur

Abstract

BACKGROUND

Both in vitro and in vivo studies indicate that homocysteine (Hcy) may be directly involved in the damage of motor neurons and in several pathways implicated in amyotrophic lateral sclerosis (ALS) pathogenesis.

OBJECTIVE

To determine whether plasma Hcy levels were higher in ALS patients than healthy controls and to examine the relationship between Hcy levels and clinical ALS phenotypes.

METHODS

In a cross-sectional study, we compared Hcy, B(12), and folate levels in 62 patients with ALS and 88 age- and sex-matched controls recruited as outpatients in a tertiary clinical center.

RESULTS

Patients with ALS had higher median plasma Hcy levels (11.2 [range 5.8 to 46] vs 9.7 [range 4.5 to 15.9] micromol/L; p = 0.0004) and lower folate levels (4.4 [range 1.7 to 22.1] vs 5.8 [range 2.3 to 21.1] ng/mL; p = 0.0003), compared with controls. Multivariate logistic regression revealed a strong direct association between plasma Hcy levels and presence of ALS (odds ratios adjusted for age, sex, and B-vitamin levels comparing the top tertile [Hcy levels >or= 11.6 micromol/L] with the bottom tertile [Hcy levels < 9.2 micromol/L]: 6.4; 95% CI 2.2 to 19.1; p for trend = 0.0008). We also found a trend for higher Hcy levels in patients with shorter interval from symptom onset to diagnosis (ODI; <14 months), compared with patients with longer ODI (>14 months; median Hcy levels 11.8 [range 5.8 to 46] vs 10.1 [range 7.2 to 17.6] micromol/L; p = 0.09). In a multivariate model, Hcy levels strongly correlated with shorter interval onset diagnosis (r(2) = 0.18; p = 0.01).

CONCLUSIONS

Plasma homocysteine (Hcy) levels were significantly increased in patients with amyotrophic lateral sclerosis (ALS) compared with healthy controls. ALS cases with shorter time to diagnosis presented higher Hcy levels, suggesting that higher Hcy may be linked to faster progression of the disease.

Authors+Show Affiliations

Operative Unit of Neurology, Lorenzo Bonomo Hospital, Andria, Italy.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Comparative Study
Journal Article

Language

eng

PubMed ID

18195267

Citation

Zoccolella, S, et al. "Elevated Plasma Homocysteine Levels in Patients With Amyotrophic Lateral Sclerosis." Neurology, vol. 70, no. 3, 2008, pp. 222-5.
Zoccolella S, Simone IL, Lamberti P, et al. Elevated plasma homocysteine levels in patients with amyotrophic lateral sclerosis. Neurology. 2008;70(3):222-5.
Zoccolella, S., Simone, I. L., Lamberti, P., Samarelli, V., Tortelli, R., Serlenga, L., & Logroscino, G. (2008). Elevated plasma homocysteine levels in patients with amyotrophic lateral sclerosis. Neurology, 70(3), 222-5. https://doi.org/10.1212/01.wnl.0000297193.53986.6f
Zoccolella S, et al. Elevated Plasma Homocysteine Levels in Patients With Amyotrophic Lateral Sclerosis. Neurology. 2008 Jan 15;70(3):222-5. PubMed PMID: 18195267.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Elevated plasma homocysteine levels in patients with amyotrophic lateral sclerosis. AU - Zoccolella,S, AU - Simone,I L, AU - Lamberti,P, AU - Samarelli,V, AU - Tortelli,R, AU - Serlenga,L, AU - Logroscino,G, PY - 2008/1/16/pubmed PY - 2008/2/15/medline PY - 2008/1/16/entrez SP - 222 EP - 5 JF - Neurology JO - Neurology VL - 70 IS - 3 N2 - BACKGROUND: Both in vitro and in vivo studies indicate that homocysteine (Hcy) may be directly involved in the damage of motor neurons and in several pathways implicated in amyotrophic lateral sclerosis (ALS) pathogenesis. OBJECTIVE: To determine whether plasma Hcy levels were higher in ALS patients than healthy controls and to examine the relationship between Hcy levels and clinical ALS phenotypes. METHODS: In a cross-sectional study, we compared Hcy, B(12), and folate levels in 62 patients with ALS and 88 age- and sex-matched controls recruited as outpatients in a tertiary clinical center. RESULTS: Patients with ALS had higher median plasma Hcy levels (11.2 [range 5.8 to 46] vs 9.7 [range 4.5 to 15.9] micromol/L; p = 0.0004) and lower folate levels (4.4 [range 1.7 to 22.1] vs 5.8 [range 2.3 to 21.1] ng/mL; p = 0.0003), compared with controls. Multivariate logistic regression revealed a strong direct association between plasma Hcy levels and presence of ALS (odds ratios adjusted for age, sex, and B-vitamin levels comparing the top tertile [Hcy levels >or= 11.6 micromol/L] with the bottom tertile [Hcy levels < 9.2 micromol/L]: 6.4; 95% CI 2.2 to 19.1; p for trend = 0.0008). We also found a trend for higher Hcy levels in patients with shorter interval from symptom onset to diagnosis (ODI; <14 months), compared with patients with longer ODI (>14 months; median Hcy levels 11.8 [range 5.8 to 46] vs 10.1 [range 7.2 to 17.6] micromol/L; p = 0.09). In a multivariate model, Hcy levels strongly correlated with shorter interval onset diagnosis (r(2) = 0.18; p = 0.01). CONCLUSIONS: Plasma homocysteine (Hcy) levels were significantly increased in patients with amyotrophic lateral sclerosis (ALS) compared with healthy controls. ALS cases with shorter time to diagnosis presented higher Hcy levels, suggesting that higher Hcy may be linked to faster progression of the disease. SN - 1526-632X UR - https://www.unboundmedicine.com/medline/citation/18195267/Elevated_plasma_homocysteine_levels_in_patients_with_amyotrophic_lateral_sclerosis_ L2 - http://www.neurology.org/cgi/pmidlookup?view=long&amp;pmid=18195267 DB - PRIME DP - Unbound Medicine ER -