Steroid 21-hydroxylase gene variants and late-life depression

被引:1
|
作者
Ancelin, Marie-Laure [1 ]
Norton, Joanna [1 ]
Ritchie, Karen [1 ,2 ]
Chaudieu, Isabelle [1 ]
Ryan, Joanne [3 ]
机构
[1] Univ Montpellier, INSERM, INM, Montpellier, France
[2] Univ Edinburgh, Ctr Clin Brain Sci, Edinburgh, Midlothian, Scotland
[3] Monash Univ, Biol Neuropsychiat & Dementia Unit, Sch Publ Hlth & Prevent Med, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
Late-life depression; Older adults; Population-based study; Stress; Corticosteroids; Single-nucleotide polymorphisms; CONGENITAL ADRENAL-HYPERPLASIA; SEX-DIFFERENCES; HPA AXIS; VULNERABILITY; DEFICIENCY;
D O I
10.1186/s13104-021-05616-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objectives A feature of late-life depression is alterations of the stress hormone system. The CYP21A2 gene encodes for the steroid 21-hydroxylase enzyme which is required for the biosynthesis of mineralocorticoids and glucocorticoids, two main components of the stress response in humans. Variants in the CYP21A2 gene could influence risk of late-life depression, but this has not been examined. This study investigated possible associations between five variants in the CYP21A2 gene and late-life depression in 1007 older community-dwelling men and women. Results In multivariate logistic regression model, significant associations were found between three single-nucleotide polymorphisms (rs389883, rs437179, and rs630379) and depression in women specifically (OR ranging from 1.51 to 1.68, p-values 0.025 to 0.0045), and the two latter remained significant after correction for multiple testing. Variants of the CYP21A2 gene appear as susceptibility factors for late-life depression in a sex-specific manner, independently of somatic and neuropsychiatric comorbidity.
引用
收藏
页数:6
相关论文
共 50 条
  • [1] Steroid 21-hydroxylase gene variants and late-life depression
    Marie-Laure Ancelin
    Joanna Norton
    Karen Ritchie
    Isabelle Chaudieu
    Joanne Ryan
    BMC Research Notes, 14
  • [2] HAPLOTYPES OF THE STEROID 21-HYDROXYLASE GENE REGION ENCODING MILD STEROID 21-HYDROXYLASE DEFICIENCY
    HAGLUNDSTENGLER, B
    RITZEN, EM
    GUSTAFSSON, J
    LUTHMAN, H
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (19) : 8352 - 8356
  • [3] GENE CONVERSION IN STEROID 21-HYDROXYLASE GENES
    URABE, K
    KIMURA, A
    HARADA, F
    IWANAGA, T
    SASAZUKI, T
    AMERICAN JOURNAL OF HUMAN GENETICS, 1990, 46 (06) : 1178 - 1186
  • [4] GENE CONVERSION IN STEROID 21-HYDROXYLASE GENES
    URABE, K
    KIMURA, A
    IWANAGA, T
    YASUNAMI, M
    SASAZUKI, T
    JAPANESE JOURNAL OF HUMAN GENETICS, 1988, 33 (02): : 273 - 273
  • [5] ANALYSIS OF STEROID 21-HYDROXYLASE GENE IN 5 UNRELATED JAPANESE PATIENTS WITH 21-HYDROXYLASE DEFICIENCY
    NAKURA, J
    MIKI, T
    FUKUCHI, K
    SHIMIZU, K
    NOSE, O
    TAKAI, S
    WHITE, PC
    HONJO, T
    KUMAHARA, Y
    ENDOCRINOLOGIA JAPONICA, 1987, 34 (03): : 373 - 379
  • [6] EVIDENCE FOR FREQUENT GENE CONVERSION IN THE STEROID 21-HYDROXYLASE P-450(C21) GENE - IMPLICATIONS FOR STEROID 21-HYDROXYLASE DEFICIENCY
    HIGASHI, Y
    TANAE, A
    INOUE, H
    FUJIIKURIYAMA, Y
    AMERICAN JOURNAL OF HUMAN GENETICS, 1988, 42 (01) : 17 - 25
  • [7] CHARACTERIZATION OF A REGULATORY REGION OF THE STEROID 21-HYDROXYLASE GENE
    PARKER, KL
    SCHIMMER, BP
    CHAPLIN, DD
    SEIDMAN, JG
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1986, 261 (33) : 5353 - 5355
  • [8] HETEROGENEITY IN THE GENE LOCUS FOR STEROID 21-HYDROXYLASE DEFICIENCY
    RUMSBY, G
    FIELDER, AHL
    HAGUE, WM
    HONOUR, JW
    JOURNAL OF MEDICAL GENETICS, 1988, 25 (09) : 596 - 599
  • [9] Aromatase (CYP19A1) gene variants, sex steroid levels, and late-life depression
    Ancelin, Marie-Laure
    Norton, Joanna
    Canonico, Marianne
    Scarabin, Pierre-Yves
    Ritchie, Karen
    Ryan, Joanne
    DEPRESSION AND ANXIETY, 2020, 37 (02) : 146 - 155
  • [10] Microsatellite markers in the indirect analysis of the steroid 21-hydroxylase gene
    Ezquieta, B
    Jariego, C
    Varela, JM
    Oliver, A
    Gracia, R
    PRENATAL DIAGNOSIS, 1997, 17 (05) : 429 - 434