PMID- 11735095 OWN - NLM STAT- MEDLINE DCOM- 20020102 LR - 20220409 IS - 0026-0495 (Print) IS - 0026-0495 (Linking) VI - 50 IP - 12 DP - 2001 Dec TI - Hyperhomocysteinemia and related factors in 600 hospitalized elderly subjects. PG - 1466-71 AB - Hyperhomocysteinemia (HHcy) is a metabolic disorder frequently occurring in the elderly population. Recently several reports have suggested abnormalities in homocysteine (tHcy) metabolism implicating HHcy as a metabolic link in the multifactorial processes characterizing many geriatric illnesses-with special emphasis on atherosclerotic vascular diseases and cognitive impairment. The present study was undertaken in a large sample of elderly hospitalized subjects to determine (1) the prevalence of HHcy, (2) the association of HHcy with vascular and cognitive disorders, and (3) the factors independently predicting Hhcy. Six hundred elderly subjects (264 men and 336 women; mean age, 79 +/- 9 years) were randomly chosen from those admitted as inpatients over a period of 3 years. In all patients, body mass index (BMI), mid-upper arm muscle area (MUAMA), plasma cholesterol, triglycerides, total proteins, albumin, lymphocyte count, creatinine, homocysteine (fasting and 4 hours after methionine oral load), serum vitamin B(6), vitamin B(12), and folate concentrations were measured. The presence of disease or use of medications known to affect homocysteine plasma levels were also recorded. The mean fasting tHcy level was 16.8 +/- 12 micromol/L in the whole sample, 18.18 +/- 13.25 micromol/L in men, and 15.86 +/- 12.14 micromol/L in women (P =.005 men v women). The mean Hcy level 4 hours after methionine load was 37.95 +/- 20.9 in the whole sample. Prevalence of hyperhomocysteinemia (fasting Hcy > or = 15 micromol/L or 4 hours after methionine load > or = 35 micromol/L) was 61% (365/600) (67% in men and 56% in women, P <.05). HHcy was rarely (8%) an isolated disorder; in addition to diabetes (20%), renal failure (48.2%), and malnutrition (20.2%), it was often associated with heart failure (30%), malignancies (20.5%), and the use of diuretics (56%) and anticonvulsant drugs (13%). Plasma homocysteine progressively increases across subjects from those with no diabetes, malnutrition, renal failure, obesity, inflammatory bowel disease, heart failure to those with 1, 2, or more concurrent diseases. Multiple stepwise regression analysis showed that 72% of plasma total fasting tHcy variability was explained by age, serum folate, plasma albumin, use of diuretics, and renal function (measured as plasma creatinine clearance). In conclusion, the present study documents that hyperhomocysteinemia, in elderly hospitalized patients is (1) a common finding, (2) frequently associated with vascular and cognitive disorders, and (3) probably a secondary phenomenon in most cases. The major predictor of high plasma homocysteine levels were age, serum folate, plasma albumin, plasma creatinine clearance, and use of diuretic drugs. These variables explain a large proportion of plasma Hcy variability. CI - Copyright 2001 by W.B. Saunders Company FAU - Ventura, P AU - Ventura P AD - Department of Internal Medicine, University of Modena and Reggio Emilia, Modena, Italy. FAU - Panini, R AU - Panini R FAU - Verlato, C AU - Verlato C FAU - Scarpetta, G AU - Scarpetta G FAU - Salvioli, G AU - Salvioli G LA - eng PT - Journal Article PL - United States TA - Metabolism JT - Metabolism: clinical and experimental JID - 0375267 RN - 0LVT1QZ0BA (Homocysteine) RN - AE28F7PNPL (Methionine) SB - IM MH - Aged MH - Aged, 80 and over MH - *Aging MH - Dementia/complications MH - Diabetes Complications MH - Fasting MH - Female MH - Homocysteine/blood MH - Humans MH - Hyperhomocysteinemia/complications/*epidemiology MH - Inflammatory Bowel Diseases/complications MH - Kinetics MH - Linear Models MH - Male MH - Methionine MH - Nutrition Disorders/complications MH - Odds Ratio MH - Renal Insufficiency/complications MH - Vascular Diseases/complications EDAT- 2001/12/06 10:00 MHDA- 2002/01/05 10:01 CRDT- 2001/12/06 10:00 PHST- 2001/12/06 10:00 [pubmed] PHST- 2002/01/05 10:01 [medline] PHST- 2001/12/06 10:00 [entrez] AID - S0026-0495(01)07417-0 [pii] AID - 10.1053/meta.2001.28079 [doi] PST - ppublish SO - Metabolism. 2001 Dec;50(12):1466-71. doi: 10.1053/meta.2001.28079.