Autor segons l'article: Colomina J, Cavallé-Busquets P, Fernàndez-Roig S, Solé-Navais P, Fernandez-Ballart J, Ballesteros M, Ueland P, Meyer K, Murphy M
Departament: Ciències Mèdiques Bàsiques
e-ISSN: 2072-6643
Autor/s de la URV: Fernández Ballart, Joan Domènech / Murphy, Michelle
Paraules clau: Synthase Risk Pregnancy Plasma homocysteine Methionine metabolism Mammals Homocysteine methyltransferase Gene-expression Folic-acid supplementation Folate Down-syndrome Dimethylglycine Bhmt c.716g>a Bhmt c.716g > a Betaine: homocysteine methyltransferase Betaine Association folate bhmt c.716g> dimethylglycine betaine: homocysteine methyltransferase betaine a
Resum: The effect of the betaine: homocysteine methyltransferase BHMT c.716G>A (G: guanosine; A: adenosine) single nucleotide polymorphism (SNP) on the BHMT pathway is unknown during pregnancy. We hypothesised that it impairs betaine to dimethylglycine conversion and that folate status modifies its effect. We studied 612 women from the Reus Tarragona Birth Cohort from ¿12 gestational weeks (GW) throughout pregnancy. The frequency of the variant BHMT c.716A allele was 30.8% (95% confidence interval (CI): 28.3, 33.5). In participants with normal-high plasma folate status (>13.4 nmol/L), least square geometric mean [95% CI] plasma dimethylglycine (pDMG, µmol/L) was lower in the GA (2.35 [2.23, 2.47]) versus GG (2.58 [2.46, 2.70]) genotype at ¿12 GW (p < 0.05) and in the GA (2.08 [1.97, 2.19]) and AA (1.94 [1.75, 2.16]) versus GG (2.29 [2.18, 2.40]) genotypes at 15 GW (p < 0.05). No differences in pDMG between genotypes were observed in participants with possible folate deficiency (¿13.4 µmol/L) (p for interactions at ¿12 GW: 0.023 and 15 GW: 0.038). PDMG was lower in participants with the AA versus GG genotype at 34 GW (2.01 [1.79, 2.25] versus 2.44 [2.16, 2.76] and at labour, 2.51 [2.39, 2.64] versus 3.00 [2.84, 3.18], (p < 0.01)). Possible deficiency compared to normal-high folate status was associated with higher pDMG in multiple linear regression analysis (¿ coefficients [SEM] ranging from 0.07 [0.04], p < 0.05 to 0.20 [0.04], p < 0.001 in models from early and mid-late pregnancy) and the AA compared to GG genotype was associated with lower pDMG (¿ coefficients [SEM] ranging from -0.11 [0.06], p = 0.055 to -0.23 [0.06], p < 0.001). Conclusion: During pregnancy, the BHMT pathway is affected by folate status and by the variant BHMT c.716A allele.
Àrees temàtiques: Zootecnia / recursos pesqueiros Saúde coletiva Química Psicología Planejamento urbano e regional / demografia Nutrition and dietetics Nutrition & dietetics Nutrição Medicina veterinaria Medicina iii Medicina ii Medicina i Interdisciplinar Food science Farmacia Engenharias iv Engenharias ii Enfermagem Educação física Economia Ciências biológicas iii Ciências biológicas ii Ciências biológicas i Ciências agrárias i Ciência de alimentos Biotecnología
Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
ISSN: 20726643
Adreça de correu electrònic de l'autor: michelle.murphy@urv.cat
Identificador de l'autor: 0000-0002-6304-6204
Data d'alta del registre: 2024-09-07
Volum de revista: 8
Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
Enllaç font original: https://www.mdpi.com/2072-6643/8/10/621
URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
Referència a l'article segons font original: Nutrients. 8 (10):
Referència de l'ítem segons les normes APA: Colomina J, Cavallé-Busquets P, Fernàndez-Roig S, Solé-Navais P, Fernandez-Ballart J, Ballesteros M, Ueland P, Meyer K, Murphy M (2016). Maternal folate status and the BHMT c.716g>A polymorphism affect the betaine dimethylglycine pathway during pregnancy. Nutrients, 8(10), -. DOI: 10.3390/nu8100621
DOI de l'article: 10.3390/nu8100621
Entitat: Universitat Rovira i Virgili
Any de publicació de la revista: 2016
Tipus de publicació: Journal Publications
Repositori URV