Association of RMND1/CCDC170-ESR1 single nucleotide polymorphisms with hip fracture and osteoporosis in postmenopausal women.
Absorptiometry, Photon
Aged
Bone Density
/ genetics
Carrier Proteins
/ genetics
Cell Cycle Proteins
/ genetics
Cohort Studies
Estrogen Receptor alpha
/ genetics
Female
Gene Frequency
Haplotypes
Hip Fractures
/ genetics
Humans
Linear Models
Linkage Disequilibrium
Mexico
Middle Aged
Osteoporosis, Postmenopausal
/ genetics
Pelvic Bones
/ pathology
Polymorphism, Single Nucleotide
Postmenopause
Osteoporosis
bone mineral density
genetic association
hip fracture
single nucleotide polymorphism
Journal
Climacteric : the journal of the International Menopause Society
ISSN: 1473-0804
Titre abrégé: Climacteric
Pays: England
ID NLM: 9810959
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
pubmed:
3
1
2019
medline:
16
4
2020
entrez:
3
1
2019
Statut:
ppublish
Résumé
This study aimed to investigate the association of seven single nucleotide polymorphisms (SNPs) on the RMND1, CCDC170, and ESR1 genes with osteoporosis or hip fracture in a postmenopausal Mexican population. We included a group of 400 postmenopausal women from the Health Workers Cohort Study from the Mexican Institute of Social Security. As a replication sample, we recruited 423 postmenopausal women from the National Institute of Rehabilitation. Demographic data were collected through a structured questionnaire. Bone mineral density was assessed using dual X-ray absorptiometry. Individuals were classified as normal, osteopenia, osteoporosis, and fracture, according to World Health Organization criteria. Genotyping was performed using predesigned TaqMan Probes. Linear regression analysis was used to investigate association. All of the analyzed SNPs showed association with at least one of the phenotypes of the study groups. In addition, we observed a region with linkage disequilibrium within the ESR1 gene in all groups. This study shows that an association of the SNPs can exist with osteopenia, osteoporosis, or fragility fracture. Our results agree with data published elsewhere, supporting the potential of these loci for the identification of the population at risk. However, additional studies are required to determine the extent of this association for other geographic regions of Mexico.
Identifiants
pubmed: 30601066
doi: 10.1080/13697137.2018.1538339
doi:
Substances chimiques
CCDC170 protein, human
0
Carrier Proteins
0
Cell Cycle Proteins
0
ESR1 protein, human
0
Estrogen Receptor alpha
0
RMND1 protein, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM