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*
Division of General Internal Medicine, Memorial Hospital of Rhode Island,
Providence, Rhode Island.
Tufts Jean Mayer USDA Human Nutrition Research Center on Aging, Boston,
Massachusetts.
Division of Renal Diseases, Rhode Island Hospital, Providence, Rhode
Island.
§
Lipid Research Laboratory, The Miriam Hospital, Providence, Rhode
Island.
Correspondence to Dr. Andrew G. Bostom, Division of General Internal Medicine, Memorial Hospital of Rhode Island, 111 Brewster Street, Pawtucket, RI 02860. Phone: 401-729-2859; Fax: 401-729-2950; E-mail: abostom{at}loa.com
Abstract
Abstract. Serum creatinine, a surrogate for both renal function
and homocysteine generation, is an important determinant of fasting plasma
total homocysteine levels in stable renal transplant recipients. In this
study, it is hypothesized that among stable renal transplant recipients with
normal creatinine levels (i.e.,
1.5 mg/dl), serum cystatin C, a
more sensitive indicator of GFR, would better predict fasting total
homocysteine levels compared with serum creatinine. Fasting plasma total
homocysteine, folate, vitamin B12, and pyridoxal 5'-phosphate
levels, along with serum cystatin C, creatinine, and albumin levels, were
determined in 28 consecutive renal transplant recipients (mean age 47 ±
14 yr; 60.7% men) with stable allograft function, whose serum creatinine was
1.5 mg/dl. General linear modeling with analysis of covariance revealed
that serum cystatin C was independently predictive (partial R =
0.494; P = 0.023) of fasting total homocysteine levels after
adjustment for age, gender, vitamin status, albumin, and creatinine levels. In
contrast, creatinine levels were not predictive of fasting total homocysteine
levels in this model (P = 0.110) or an identical model that excluded
cystatin C (P = 0.131). Serum cystatin C levels may reflect subtle
decreases in renal function that independently predict fasting total
homocysteine levels among stable renal transplant recipients with a normal
serum creatinine.
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