Autor(es):
Katler, Q ; Stepien, K ; Paull, N ; Patel, S ; Adams, M ; Balci, M ; Berry, G ; Bosch, A ; DeLaO, A ; Demirbas, D ; Edman, J ; Ficicioglu, C ; Goff, M ; Hacker, S ; Knerr, I ; Lancaster, K ; Li, H ; Mendelsohn, B ; Nichols, B ; Rezende Pinto, W ; César Rocha, J ; Rubio‐Gozalbo, ME ; Saad‐Naguib, M ; Scholl‐Buergi, S ; Searcy, S ; Souza, P ; Wittenauer, A ; Fridovich‐Keil, J
Data: 2022
Identificador Persistente: http://hdl.handle.net/10400.17/4715
Origem: Repositório do Centro Hospitalar de Lisboa Central, EPE
Assunto(s): HCC END; Humans; Female; Alleles; Galactose; Galactosemias* / diagnosis; Galactosemias* / genetics; Homozygote; Infant, Newborn; UTP-Hexose-1-Phosphate Uridylyltransferase / genetics
Descrição
Patients with galactosemia who carry the S135L (c.404C > T) variant of galactose-1-P uridylyltransferase (GALT), documented to encode low-level residual GALT activity, have been under-represented in most prior studies of outcomes in Type 1 galactosemia. What is known about the acute and long-term outcomes of these patients, therefore, is based on very limited data. Here, we present a study comparing acute and long-term outcomes of 12 patients homozygous for S135L, 25 patients compound heterozygous for S135L, and 105 patients homozygous for two GALT-null (G) alleles. This is the largest cohort of S135L patients characterized to date. Acute disease following milk exposure in the newborn period was common among patients in all 3 comparison groups in our study, as were long-term complications in the domains of speech, cognition, and motor outcomes. In contrast, while at least 80% of both GALT-null and S135L compound heterozygous girls and women showed evidence of an adverse ovarian outcome, prevalence was only 25% among S135L homozygotes. Further, all young women in this study with even one copy of S135L achieved spontaneous menarche; this is true for only about 33% of women with classic galactosemia. Overall, we observed that while most long-term outcomes trended milder among groups of patients with even one copy of S135L, many individual patients, either homozygous or compound heterozygous for S135L, nonetheless experienced long-term outcomes that were not mild. This was true despite detection by newborn screening and both early and life-long dietary restriction of galactose. This information should empower more evidence-based counseling for galactosemia patients with S135L.
