PMID- 10760109 OWN - NLM STAT- MEDLINE DCOM- 20000509 LR - 20131121 IS - 0085-2538 (Print) IS - 0085-2538 (Linking) VI - 57 IP - 4 DP - 2000 Apr TI - Hyperhomocysteinemia, nutritional status, and cardiovascular disease in hemodialysis patients. PG - 1727-35 AB - BACKGROUND: Hyperhomocysteinemia, cardiovascular disease (CVD), and malnutrition are common in patients with end-stage renal disease (ESRD). This study was designed to assess possible relationships between total plasma homocysteine (tHcy), nutritional status, and ischemic CVD. METHODS: We performed a cross-sectional study in 117 unselected patients on maintenance hemodialysis (HD) treatment, among whom there was a high prevalence of malnutrition (56%), as assessed by the subjective global nutritional assessment (SGNA), and a high prevalence of CVD (60%), and prospectively, we followed-up the overall mortality for four years. RESULTS: The level of tHcy was elevated in 95% of the HD patients, and that of total plasma cysteine (tCys) was also significantly elevated, while the plasma concentrations of methionine (Met), serine (Ser), and taurine (Tau) were significantly lower than those in healthy controls. The 65 patients who were malnourished according to the SGNA score had significantly lower levels of serum albumin (SAlb), plasma IFG-1 (p-IGF-1), tHcy, tCys, and Met than the 52 patients with normal nutritional status, whereas the levels of Ser, Tau, plasma folate, and vitamin B12 were similar in the two groups. The prevalence of malnutrition was 30% in the 47 patients without CVD and was significantly higher (70%, P < 0.001) in the 70 patients with CVD, who also had lower tHcy, SAlb, plasma IGF-1, serum creatinine (SCr), and blood hemoglobin. The tHcy levels were positively correlated with SAlb, Met, tCys, and SCr. Stepwise, multiple-regression analysis showed that tCys, SAlb, and normalized protein equivalent of nitrogen appearance (nPNA), an indicator of protein intake, were independent predictors of tHcy. The patients with tHcy <24 micromol/L (median value) had a significantly worse four-year survival than those with a higher tHcy (> or =24 micromol/L). CONCLUSIONS: Our results demonstrate that most of HD patients have grossly elevated tHcy levels, but that the absolute level appears to be dependent on nutritional status, protein intake, and SAlb. The results also suggest that the lower tHcy levels in patients with CVD than in those without CVD may be related to the higher prevalence of malnutrition and hypoalbuminemia in the CVD patients. This is also in accordance with our observation that the patients with lower tHcy had a worse survival rate than those with higher tHcy, considering that malnutrition is a strong risk factor for mortality and that CVD is the most common cause of death in ESRD patients. FAU - Suliman, M E AU - Suliman ME AD - Divisions of Baxter Novum and Renal Medicine, Department of Clinical Science, Karolinska Institutet, Huddinge University Hospital, Stockholm, Sweden. FAU - Qureshi, A R AU - Qureshi AR FAU - Barany, P AU - Barany P FAU - Stenvinkel, P AU - Stenvinkel P FAU - Filho, J C AU - Filho JC FAU - Anderstam, B AU - Anderstam B FAU - Heimburger, O AU - Heimburger O FAU - Lindholm, B AU - Lindholm B FAU - Bergstrom, J AU - Bergstrom J LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Kidney Int JT - Kidney international JID - 0323470 RN - 0 (Amino Acids) RN - 0 (Dietary Proteins) RN - 0 (Serum Albumin) RN - K848JZ4886 (Cysteine) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Amino Acids/blood MH - Cardiovascular Diseases/*complications/physiopathology MH - Cross-Sectional Studies MH - Cysteine/blood MH - Dietary Proteins/administration & dosage MH - Female MH - Humans MH - Hyperhomocysteinemia/*complications MH - Kidney Failure, Chronic/complications/mortality/physiopathology/therapy MH - Male MH - Middle Aged MH - Nutrition Disorders/complications MH - *Nutritional Status MH - Prospective Studies MH - *Renal Dialysis MH - Serum Albumin/analysis MH - Survival Analysis EDAT- 2000/04/12 09:00 MHDA- 2000/05/16 09:00 CRDT- 2000/04/12 09:00 PHST- 2000/04/12 09:00 [pubmed] PHST- 2000/05/16 09:00 [medline] PHST- 2000/04/12 09:00 [entrez] AID - S0085-2538(15)46923-6 [pii] AID - 10.1046/j.1523-1755.2000.00018.x [doi] PST - ppublish SO - Kidney Int. 2000 Apr;57(4):1727-35. doi: 10.1046/j.1523-1755.2000.00018.x.