Leukocyte phosphomannomutase activity in diagnosis of congenital disorder of glycosylation Ia.

Phosphomannomutase (PMM; EC 5.4.2.8) is a cytosolic enzyme that catalyzes the reversible conversion of mannose 6-phosphate to mannose 1-phosphate, a substrate for the synthesis of GDP-mannose, which is a nucleotide sugar required in glycosylation. Previously known in yeast (1, 2), Van Schaftingen and Jaeken (3 ) described the enzyme in 1995 in humans and its deficiency in patients with congenital disorders of glycosylation (CDG) Ia, an autosomal recessive disorder characterized by psychomotor retardation and multisystemic involvement (4 ). PMM deficiency is related to the presence of mutations in the corresponding PMM2 gene (5 ). Most patients bear the very common R141H mutation, which is never found in the homozygous state because it is probably lethal (6 ). Diagnosis of CDG Ia, screening for which involves evidence of abnormally glycosylated serum N-glycoproteins (7 ), is completed by measurement of cellular PMM activity. Authors who have published PMM activity results (3, 8–13) have worked primarily on cultured fibroblasts and lymphoblasts or peripheral blood mononucleated cells (PBMCs). However, in most studies, the analytical conditions are described rather succinctly, no indication is given of the preanalytical conditions, and well-defined reference values are lacking. The aim of this study was to determine preanalytical conditions for the PMM assay measured in PBMCs from healthy individuals and the corresponding reference values, and to compare them with the results obtained for CDG Ia patients and their relatives. Deindentified blood samples were obtained (from January 1999 to January 2001) from 414 individuals without CDG I (control group; age range, 1 month to 87 years), 25 CDG Ia patients for whom diagnosis was confirmed by the identification of PMM2 mutations, and 35 of their parents or relatives bearing one mutation on the PMM2 gene. PBMCs were first isolated on a Ficoll gradient (14 ). Cell pellets were resuspended in the homogenization buffer [20 mmol/L HEPES, 10 mmol/L KCl, 1.5 mmol/L MgCl2, 1 mmol/L dithiothreitol, 0.25 mol/L sucrose, and antiproteases (10 mg/L each of Trasyslol, leupeptin, and phenylmethylsulfonyl fluoride)] and were lysed mechanically by numerous passes through a syringe needle (25-gauge, 5/8-inch) and then centrifuged at 500g for 10 min. The resulting extract was used for the PMM enzymatic assay, as described elsewhere (3 ), and protein determination (15 ). PMM results are expressed as mean SD U/g of total protein content (TP). Mutations on the PMM2 gene were identified by a combination of direct sequencing and restriction analysis, as described elsewhere (16 ). The means of the three groups were compared by ANOVA, followed by a post hoc test for pairwise comparison. Receiver operator characteristic (ROC) curves were calculated using the logistic procedure of SAS (SAS Institute). We first established preanalytical conditions to standardize the PMM assay conditions for samples. Dipotassium EDTA was chosen as anticoagulant because values obtained for dipotassium EDTA-blood samples were statistically higher than those obtained for paired lithium heparinate samples (n 6; P 0.032). We studied the stability of PMM activity in whole blood samples. PMM activity was measured once a day for 6 days in samples stored at 4 °C and room temperature (n 5) and compared with the activity measured directly after withdrawal on day 0. No statistical difference was found between days 0 and 1, whatever the storage temperature. In contrast, results were lower from day 2 at both temperatures (P 0.028). The time between blood withdrawal and isolation of PBMCs should be at most 24 h at room temperature. PMM activity in cell extracts was altered after day 4 in extracts stored without glycerol at 4 °C (n 6; day 0, 4.3 0.07 U/g TP; day 4, 2.3 0.04 U/g TP; P 0.001), whereas no alteration was observed when the cell extract was stored with 150 mL/L glycerol at 80 °C for at least 1 month. The within-run imprecision (CV), estimated with four successive assays of two control samples (5.3 0.2 and 4.5 0.3 U/g TP) on the same day, was 7%. The mean between-run CV was 4%, as determined by assaying the same cell extract (4.2 0.2 U/g TP) for 14 consecutive days. Using the above-mentioned assay conditions, we measured PMM activity in PBMC extracts in the different groups (Fig. 1). PMM activity in the PBMC extract from the control groups is reported in Table 1. PMM values were higher in individuals younger than 2 years compared with older individuals (P 0.001). For individuals older than 2 years, the mean PMM value was similar to those reported in other studies (8–13). The PMM mean value was lower in women (n 209; 4.8 1.3 U/g TP) than in men (n 206; 5.1 1.6 U/g TP; P 0.029). However, no difference was found in individuals younger than 2 years. To check that the assay measured PMM activity and not phosphoglucomutase (PGM), we tested the effect of arsenate (5 mmol/L) added to the assay mixture on PBMC extracts from the control groups. The PMM activity was slightly inhibited by arsenate, regardless of the sex or age of the individual (Table 1). The mean PMM activity for CDG Ia patients was significantly lower compared with the control group (P 0.0001; Table 1), although individual values varied from undetectable or residual activity up to 1.9 U/g TP. When detectable PMM activity was determined in the presence of arsenate, partial inhibition was also observed. Heterozygotes had intermediate PMM activity values, Technical Briefs