PMID- 31371071 OWN - NLM STAT- MEDLINE DCOM- 20200220 LR - 20200220 IS - 1532-2777 (Electronic) IS - 0306-9877 (Linking) VI - 129 DP - 2019 Aug TI - A novel approach in the management of hyperhomocysteinemia. PG - 109245 LID - S0306-9877(19)30367-6 [pii] LID - 10.1016/j.mehy.2019.109245 [doi] AB - Hyperhomocysteinemia (Hhcy) is a biochemical alteration with plasma levels of homocysteine higher than 15 micromol/L, associated with atherosclerosis, and with vascular thrombosis by disrupting endothelial cells. Homocysteine is a sulfur-containing amino acid derived from methionine which is an essential amino acid. Excess homocysteine produced in the body is expelled out by liver and kidney from the systemic circulation. Hhcy is caused by the excess deficiencies of the vitamins like pyridoxine (B6), folic acid (B9), or cyanocobalamin (B12). High protein consumers are usually at risk for hyperhomocysteinemia because of low plasma B12 levels. It is approximated that mild Hhcy occurs in 5-7% of the general population and 40% in patients with vascular disease. Patients with heart failure, impaired renal function, and diabetes should be screened since the prevalence of Hhcy in these patients appears to be quite high. In this article, we hypothesise that citicoline is a novel drug for the management of Hhcy. Furthermore, the side effects of citicoline are also minimal and self-limiting. If this strategy is validated, citicoline will be the cost-effective way to be administered for Hhcy. Many evidences are available which suggest that ignoring homocysteine levels in patients with the vascular disease would be unwise. Thus, there is an urgent need for health care providers to develop effective preventions and interventions program (folic acid, Vitamin B6 and Vitamin B12 supplementation as well as lifestyle change) to reduce this disorder. CI - Copyright (c) 2019 Elsevier Ltd. All rights reserved. FAU - Qureshi, Shaiba Sana AU - Qureshi SS AD - Department of Pharmacology, Institute of Pharmaceutical Research, GLA University, Mathura 281406, UP, India. FAU - Gupta, Jeetendra Kumar AU - Gupta JK AD - Department of Pharmacology, Institute of Pharmaceutical Research, GLA University, Mathura 281406, UP, India. Electronic address: jkgupta81@rediffmail.com. FAU - Goyal, Ahsas AU - Goyal A AD - Department of Pharmacology, Institute of Pharmaceutical Research, GLA University, Mathura 281406, UP, India. FAU - Narayan Yadav, Harlokesh AU - Narayan Yadav H AD - All India Institute of Medical Sciences (AIIMS), New Delhi 110029, India. LA - eng PT - Journal Article DEP - 20190523 PL - United States TA - Med Hypotheses JT - Medical hypotheses JID - 7505668 RN - 0LVT1QZ0BA (Homocysteine) RN - 536BQ2JVC7 (Cytidine Diphosphate Choline) RN - 8059-24-3 (Vitamin B 6) RN - 935E97BOY8 (Folic Acid) RN - AE28F7PNPL (Methionine) RN - EC 1.1.- (Alcohol Oxidoreductases) RN - EC 1.1.3.17 (choline oxidase) RN - N91BDP6H0X (Choline) RN - P6YC3EG204 (Vitamin B 12) SB - IM MH - Alcohol Oxidoreductases/metabolism MH - Animals MH - Choline/therapeutic use MH - Cytidine Diphosphate Choline/therapeutic use MH - Dietary Supplements MH - Endothelial Cells MH - Folic Acid/*therapeutic use MH - Homocysteine/metabolism MH - Humans MH - Hydrolysis MH - Hyperhomocysteinemia/complications/*therapy MH - Kidney/metabolism/physiopathology MH - Life Style MH - Liver/metabolism MH - Methionine/metabolism MH - Models, Theoretical MH - Vitamin B 12/*therapeutic use MH - Vitamin B 6/*therapeutic use OTO - NOTNLM OT - Atherosclerosis OT - Citicoline OT - Hyperhomocysteinemia OT - Stroke OT - Vitamin B12 OT - Vitamin B6 EDAT- 2019/08/03 06:00 MHDA- 2020/02/23 06:00 CRDT- 2019/08/03 06:00 PHST- 2019/04/03 00:00 [received] PHST- 2019/05/22 00:00 [accepted] PHST- 2019/08/03 06:00 [entrez] PHST- 2019/08/03 06:00 [pubmed] PHST- 2020/02/23 06:00 [medline] AID - S0306-9877(19)30367-6 [pii] AID - 10.1016/j.mehy.2019.109245 [doi] PST - ppublish SO - Med Hypotheses. 2019 Aug;129:109245. doi: 10.1016/j.mehy.2019.109245. Epub 2019 May 23.