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ArticleEuropean spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society2025

Sex- and age-stratified analysis of structural risk factors for disabling chronic low back pain in a Japanese longitudinal cohort.

Shizumasa Murata, Keiji Nagata, Hiroshi Hashizume, Kanae Mure, Naomi Iwane, Hiroyuki Oka, Toshiko Iidaka, Masatoshi Teraguchi, Yuyu Ishimoto, Masanari Takami and 5 more

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Article in European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Shizumasa MurataDepartment of Orthopaedic Surgery, Wakayama Medical University, Wakayama, Japan.
Keiji Nagata *Department of Orthopaedic Surgery, Wakayama Medical University, Wakayama, Japan.
Hiroshi Hashizume *Department of Orthopaedic Surgery, Wakayama Medical University, Wakayama, Japan. hiroshi.hashizume2000@gmail.com.
Kanae MureDepartment of Public Health, Wakayama Medical University, Wakayama, Japan.
Naomi IwaneSchool of Health and Nursing Science, Wakayama Medical University, Wakayama, Japan.
Hiroyuki OkaDivision of Musculoskeletal AI System Development, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Toshiko IidakaDepartment of Preventive Medicine for Locomotive Organ Disorders, 22nd Century Medical and Research Center, The University of Tokyo, Tokyo, Japan.
Masatoshi TeraguchiDepartment of Orthopaedic Surgery, Wakayama Medical University, Wakayama, Japan.
Yuyu IshimotoDepartment of Orthopaedic Surgery, Wakayama Medical University, Wakayama, Japan.
Masanari TakamiDepartment of Orthopaedic Surgery, Wakayama Medical University, Wakayama, Japan.
Shunji TsutsuiDepartment of Orthopaedic Surgery, Wakayama Medical University, Wakayama, Japan.
Hiroshi IwasakiDepartment of Orthopaedic Surgery, Wakayama Medical University, Wakayama, Japan.
Sakae TanakaDepartment of Orthopaedic Surgery, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Hiroshi YamadaDepartment of Orthopaedic Surgery, Wakayama Medical University, Wakayama, Japan.
Noriko YoshimuraDepartment of Preventive Medicine for Locomotive Organ Disorders, 22nd Century Medical and Research Center, The University of Tokyo, Tokyo, Japan.

Funding

Challenging Exploratory Research grants 18K18447, 15K15219, and 24659317Grant-in-Aid funding from the Ministry of Health, Labour and Welfare 21FA0601Scientific Research grants 26462249Scientific Research grants B19H03895, B26293139, B23390172, and B20390182the Japan Agency for Medical Research and Development (AMED) JP22dk0110047
6 · The paper itself

Abstract

purposeDisabling chronic low back pain (DCLBP) imposes a growing burden in aging societies. Although lumbar disc degeneration (DD), vertebral fractures (VF), and lumbar spinal stenosis (LSS) are known contributors, their differential impact across age and sex remains unclear. This study aimed to identify age- and sex-specific structural risk factors for DCLBP in a Japanese community-based cohort.

methodsWe included 653 participants (219 male, 434 female; mean age 62.1 ± 13.0 years) from the Wakayama Spine Study. Baseline assessments included MRI-based DD scores, radiographic VF scores at T11-L1, and LSS severity. DCLBP at follow-up was defined as low back pain ≥ 3 months with an Oswestry Disability Index ≥ 21%. Multivariable logistic regression was conducted stratified by age (40-64, 65-74, ≥ 75) and sex. Interaction terms were included to evaluate effect modification.

resultsDCLBP was identified in 13.9% of participants, and its prevalence increased with age (9.6% in the 40-64 years group; 13.8% in the 65-74 years group; and 20.4% in the 75 years and older group). In the 40-64 years group, higher body mass index (BMI) was independently associated with DCLBP (odds ratio [OR]: 1.13; 95% confidence interval [CI]: 1.01-1.26; p = 0.033). Among participants 75 years or older, the vertebral fracture (VF) score was a strong predictor of DCLBP, particularly for female participants (OR: 1.82; 95% CI: 1.27-2.59; p = 0.001). Overall, the VF score (OR: 1.45; 95% CI: 1.16-1.81; p = 0.001) and lumbar disc degeneration score (OR: 1.19; 95% CI: 1.01-1.39; p = 0.036) of female participants were significantly associated with DCLBP. Interaction analyses revealed significant modification effects (age × VF score: p = 0.018; sex × DCLBP: p = 0.041) that suggested that the disability burden of structural spinal degeneration is particularly pronounced in older women.

conclusionRisk profiles for disabling chronic low back pain vary significantly by age and sex. Higher BMI is a key modifiable risk factor for younger adults, whereas vertebral fractures and disc degeneration are major contributors in older women. Age- and sex-tailored strategies, such as weight management during midlife and proactive fracture prevention in older women, are necessary to reduce the disability burden.

Indexed as

Chronic PainIntervertebral Disc DegenerationLow Back PainSpinal FracturesSpinal StenosisAdultAgedAge FactorsCohort StudiesEast Asian PeopleFemaleHumansJapanLongitudinal StudiesLumbar VertebraeMagnetic Resonance ImagingDisabling chronic low back painLumbar disc degenerationSpinal degenerationVertebral fractures

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.