Microalbuminuria, Lipoproteins, and Diabetic Control

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TO THE EDITOR:

In their cross-sectional analysis, Ramirez and colleagues [1] provide no data regarding microalbuminuria, nor did the preliminary studies cited by Ramirez and colleagues show either a cross-sectional (their references 30 and 32), or short-term longitudinal (their reference 31) relation between lipoprotein (a) (Lp[a]) level and glycemic control. Categorizing either insulin- or non–insulin-dependent diabetics by the presence or absence of the nephrotic syndrome is insufficient when assessing their Lp(a) levels and the possibly related risk for accelerated atherosclerotic disease.

Karadi and colleagues [2], the first to report significantly increased Lp(a) concentrations in association with nephrosis, found no correlation between daily protein loss or selectivity index and Lp(a) concentration. Jenkins and colleagues [3] reported that apolipoprotein (a) (apo [a]) levels in insulin-dependent diabetics (n = 107) were elevated in those with microalbuminuria and did not correlate with glycemic control. Patients with microalbuminuria had significantly higher apo (a) levels (geometric mean, 245 U/L compared with 196 U/L; P < 0.005), despite glycosylated hemoglobin (HbA1c) concentrations that were significantly lower than those in the albuminuric patients (mean, 8.8% compared with 9.8%; P < 0.05).

Microalbuminuria is predictive of increased mortality in non–insulin-dependent diabetes [4]. Data from the original population-based Framingham cohort suggest that trace proteinuria determined by dipstick is associated with significantly increased overall and cardiovascular disease-related mortality [5]. The interrelation of quantitative microalbuminuria, Lp(a), HbA1c, and cardiovascular disease should be examined prospectively in a population that includes persons with normal glucose tolerance, documented glucose intolerance, and overt diabetes mellitus.

Andrew G. Bostom

Peter W. F. Wilson

The Editors welcome submissions for possible publication in the Letters section. Authors of letters should:

•Include no more than 300 words of text, three authors, and five references

•Type with double-spacing

•Send three copies of the letter, an authors' form signed by all authors, and a cover letter describing any conflicts of interest related to the contents of the letter.

Letters commenting on an Annals article will be considered if they are received within 6 weeks of the time the article was published. Only some of the letters received can be published. Published letters are edited and may be shortened; tables and figures are included only selectively. Authors will be notified that the letter has been received. If the letter is selected for publication, the author will be notified about 3 weeks before the publication date. Unpublished letters cannot be returned.

Annals welcomes electronically submitted letters.

References

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