Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Sex- and age-specific genetic analysis of chronic back pain. / HUNT All-In Pain.
в: Pain, Том 162, № 4, 01.04.2021, стр. 1176-1187.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Sex- and age-specific genetic analysis of chronic back pain
AU - HUNT All-In Pain
AU - Freidin, Maxim B.
AU - Tsepilov, Yakov A.
AU - Stanaway, Ian B.
AU - Meng, Weihua
AU - Hayward, Caroline
AU - Smith, Blair H.
AU - Khoury, Samar
AU - Parisien, Marc
AU - Bortsov, Andrey
AU - Diatchenko, Luda
AU - Børte, Sigrid
AU - Winsvold, Bendik S.
AU - Brumpton, Ben M.
AU - Zwart, John Anker
AU - Aulchenko, Yurii S.
AU - Suri, Pradeep
AU - Williams, Frances M.K.
N1 - Publisher Copyright: Copyright © 2020 International Association for the Study of Pain. Copyright: This record is sourced from MEDLINE/PubMed, a database of the U.S. National Library of Medicine
PY - 2021/4/1
Y1 - 2021/4/1
N2 - Sex differences for chronic back pain (cBP) have been reported, with females usually exhibiting greater morbidity, severity, and poorer response to treatment. Genetic factors acting in an age-specific manner have been implicated but never comprehensively explored. We performed sex- and age-stratified genome-wide association study and single nucleotide polymorphism-by-sex interaction analysis for cBP defined as "Back pain for 3+ months" in 202,077 males and 237,754 females of European ancestry from UK Biobank. Two and 7 nonoverlapping genome-wide significant loci were identified for males and females, respectively. A male-specific locus on chromosome 10 near SPOCK2 gene was replicated in 4 independent cohorts. Four loci demonstrated single nucleotide polymorphism-by-sex interaction, although none of them were formally replicated. Single nucleotide polymorphism-explained heritability was higher in females (0.079 vs 0.067, P = 0.006). There was a high, although not complete, genetic correlation between the sexes (r = 0.838 ± 0.041, different from 1 with P = 7.8E-05). Genetic correlation between the sexes for cBP decreased with age (0.858 ± 0.049 in younger people vs 0.544 ± 0.157 in older people; P = 4.3E-05). There was a stronger genetic correlation of cBP with self-reported diagnosis of intervertebral disk degeneration in males than in females (0.889 vs 0.638; P = 3.7E-06). Thus, the genetic component of cBP in the UK Biobank exhibits a mild sex- and age-dependency. This provides an insight into the possible causes of sex- and age-specificity in epidemiology and pathophysiology of cBP and chronic pain at other anatomical sites.
AB - Sex differences for chronic back pain (cBP) have been reported, with females usually exhibiting greater morbidity, severity, and poorer response to treatment. Genetic factors acting in an age-specific manner have been implicated but never comprehensively explored. We performed sex- and age-stratified genome-wide association study and single nucleotide polymorphism-by-sex interaction analysis for cBP defined as "Back pain for 3+ months" in 202,077 males and 237,754 females of European ancestry from UK Biobank. Two and 7 nonoverlapping genome-wide significant loci were identified for males and females, respectively. A male-specific locus on chromosome 10 near SPOCK2 gene was replicated in 4 independent cohorts. Four loci demonstrated single nucleotide polymorphism-by-sex interaction, although none of them were formally replicated. Single nucleotide polymorphism-explained heritability was higher in females (0.079 vs 0.067, P = 0.006). There was a high, although not complete, genetic correlation between the sexes (r = 0.838 ± 0.041, different from 1 with P = 7.8E-05). Genetic correlation between the sexes for cBP decreased with age (0.858 ± 0.049 in younger people vs 0.544 ± 0.157 in older people; P = 4.3E-05). There was a stronger genetic correlation of cBP with self-reported diagnosis of intervertebral disk degeneration in males than in females (0.889 vs 0.638; P = 3.7E-06). Thus, the genetic component of cBP in the UK Biobank exhibits a mild sex- and age-dependency. This provides an insight into the possible causes of sex- and age-specificity in epidemiology and pathophysiology of cBP and chronic pain at other anatomical sites.
UR - http://www.scopus.com/inward/record.url?scp=85103226731&partnerID=8YFLogxK
U2 - 10.1097/j.pain.0000000000002100
DO - 10.1097/j.pain.0000000000002100
M3 - Article
C2 - 33021770
AN - SCOPUS:85103226731
VL - 162
SP - 1176
EP - 1187
JO - Pain
JF - Pain
SN - 0304-3959
IS - 4
ER -
ID: 28269123