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Comparative Study
. 2006 Jan;78(1):89-102.
doi: 10.1086/498985. Epub 2005 Nov 14.

Epimerase-deficiency galactosemia is not a binary condition

Affiliations
Comparative Study

Epimerase-deficiency galactosemia is not a binary condition

Kimberly K Openo et al. Am J Hum Genet. 2006 Jan.

Abstract

Epimerase-deficiency galactosemia results from the impairment of UDP-galactose 4'-epimerase (GALE), the third enzyme in the Leloir pathway of galactose metabolism. Originally identified as a clinically benign "peripheral" condition with enzyme impairment restricted to circulating blood cells, GALE deficiency was later demonstrated also to exist in a rare but clinically severe "generalized" form, with enzyme impairment affecting a range of tissues. Isolated cases of clinically and/or biochemically intermediate cases of epimerase deficiency have also been reported. We report here studies of 10 patients who, in the neonatal period, received the diagnosis of hemolysate epimerase deficiency. We have characterized these patients with regard to three parameters: (1) GALE activity in transformed lymphoblasts, representing a "nonperipheral" tissue, (2) metabolic sensitivity of those lymphoblasts to galactose challenge in culture, and (3) evidence of normal versus abnormal galactose metabolism in the patients themselves. Our results demonstrate two important points. First, whereas some of the patients studied exhibited near-normal levels of GALE activity in lymphoblasts, consistent with a diagnosis of peripheral epimerase deficiency, many did not. We detected a spectrum of GALE activity levels ranging from 15%-64% of control levels, demonstrating that epimerase deficiency is not a binary condition; it is a continuum disorder. Second, lymphoblasts demonstrating the most severe reduction in GALE activity also demonstrated abnormal metabolite levels in the presence of external galactose and, in some cases, also in the absence of galactose. These abnormalities included elevated galactose-1P, elevated UDP-galactose, and deficient UDP-glucose. Moreover, some of the patients themselves also demonstrated metabolic abnormalities, both on and off galactose-restricted diet. Long-term follow-up studies of these and other patients will be required to elucidate the clinical significance of these biochemical abnormalities and the potential impact of dietary intervention on outcome.

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Figures

Figure  1
Figure 1
Reactions catalyzed by human enzymes of the Leloir pathway of galactose metabolism
Figure  2
Figure 2
Enzyme activities in control lymphoblasts. Values plotted represent average specific activity ± SEM (N⩾3). Numbers listed above each bar are normalized to the mean of the set. C1–C10 designate the individual control cell lines studied. A, hGALE activity with regard to UDP-Gal. B, hGALE activity with regard to UDP-GalNAc. C, hGALT activity.
Figure  3
Figure 3
Enzyme activities in patient hemolysates and lymphoblasts. FKE numbers designate the individual patients enrolled in this study. A, RBC hGALE. Values plotted represent individual measurements of hemolysate hGALE specific activity with regard to UDP-Gal. Each asterisk (*) represents a missing value. Shaded area represents the control range for the assay, as reported by the clinical laboratory performing the assay. B, Lymphoblast hGALE. Values plotted represent average specific activity ± SEM (N⩾3) with regard to UDP-Gal. Numbers listed above each bar are normalized to the mean of the corresponding control set. Shaded area represents the range of corresponding control activities. C, Lymphoblast hGALE. Values plotted represent average specific activity ± SEM (N⩾3) with regard to UDP-GalNAc. Numbers listed above each bar are normalized to the mean of the corresponding control set. Shaded area represents the range of corresponding control activities. D, Lymphoblast hGALT. Values plotted represent average specific activity ± SEM (N⩾3). Numbers listed above each bar are normalized to the mean of the corresponding control set. Shaded area represents the range of corresponding control activities. Ave = average; prot = protein.
Figure  4
Figure 4
Metabolites in control and patient lymphoblasts exposed to galactose. A, External galactose in the medium of control and patient lymphoblasts at t=0 (open bar) and at t=24 h after addition of 0.5 mM galactose to the medium (shaded bar). Values plotted are average ± SEM (N⩾3). Control values were averaged from each of six different control cell lines (C1, C2, C3, C5, C7, and C10), each assayed three times. Patient cell lines designated “low,” “medium,” and “high” hGALE had <20%, 30%–40%, and >50%, respectively, of control (mean of the control set) hGALE activity with regard to UDP-Gal. B, Internal Gal-1P. Values plotted are average ± SEM (N=3) for each cell line. Open bars represent t=0; shaded bars represent t=24 h after addition of 0.5 mM galactose to the medium. C, Internal UDP-Gal. Values plotted are average ± SEM (N=3) for each cell line. Open bars represent t=0; shaded bars represent t=24 h after addition of 0.5 mM galactose to the medium. D, Internal UDP-Glc. Values plotted are average ± SEM (N=3) for each cell line. Open bars represent t=0; shaded bars represent t=24 h after addition of 0.5 mM galactose to the medium.

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References

Web Resources

    1. ExPASy, http://us.expasy.org/ (for GALK [EC 2.7.1.6], GALT [EC 2.7.7.12], and GALE [EC 5.1.3.2])
    1. GenBank, http://www.ncbi.nlm.nih.gov/Genbank/ (for hGALE reference sequences [accession numbers AF022382, NM_000403, NM_001008216, BC001273, CR616589, CR611350, CR602422, CR596991, CR592671, BC050685, L41668, CR592211, CR616462, CR601378, AL031295, DQ233667, and DQ233668])
    1. Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/entrez/Omim/

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