Risk factors for premature ovarian failure in females with galactosemia

Citation
Nv. Guerrero et al., Risk factors for premature ovarian failure in females with galactosemia, J PEDIAT, 137(6), 2000, pp. 833-841
Citations number
32
Categorie Soggetti
Pediatrics,"Medical Research General Topics
Journal title
JOURNAL OF PEDIATRICS
ISSN journal
00223476 → ACNP
Volume
137
Issue
6
Year of publication
2000
Pages
833 - 841
Database
ISI
SICI code
0022-3476(200012)137:6<833:RFFPOF>2.0.ZU;2-U
Abstract
The risk for premature ovarian failure (POF) in females with galactosemia c an be predicted by analyzing 3 areas of risk pathology: the patient's molec ular genotype for galactose-1-phosphate uridyltransferase (GALT), alternate pathways for galactose metabolism, and the patient's environment at diagno sis and during treatment. Study design: Retrospective cross-sectional information was collected on 53 females with classic galactosemia, and their ovarian function was analyzed by determination of serum follicle-stimulating hormone and luteinizing hor mone levels and by clinical observation. The associations were analyzed bet ween POF and the mutations in GALT, the highest erythrocyte galactose-1-pho sphate (Gal-1-P) level at diagnosis, the age at which dietary treatment was initialed, mean erythrocyte Gal-1-P level during treatment, and whole-body carbon 13-labeled galactose oxidation to (CO2)-C-13. Results: The most prevalent mutation, Q188R, had a significant effect of ge notype category (Q188R/Q188R, Q188R/Other, Other/Other) on POF (P = .04, Fi sher exact test and an odds ratio of 8.3). Mean erythrocyte Gal-1-P level d uring treatment was a significant risk factor for POF (P = .04). Also, all patients studied with less than 5% total body oxidation of galactose to (CO 2)-C-13 had POF whereas those with more than 5% did not have POF (P = .008, Fisher exact lest). Conclusion: The development of POF in females with galactosemia is more lik ely if the patient's genotype is Q188R/Q188R, if the mean erythrocyte Gal-1 -P is >3.5 mg/dL during therapy and if the recovery of (CO2)-C-13 from whol e-body C-13-galactose oxidation is reduced below 5% of administered C-13-ga lactose.