# Prevalence and associated factors of self-reported lifetime epilepsy symptoms in an older population in Russia: the Ural Very Old Study

**Authors:** Mukharram M. Bikbov, Gyulli M. Kazakbaeva, Ellina M. Iakupova, Leisan I. Gilemzianova, Anastasiia V. Insapova, Diana A. Timerbulatova, Songhomitra Panda-Jonas, Jost B. Jonas

PMC · DOI: 10.3389/fneur.2026.1751674 · Frontiers in Neurology · 2026-02-06

## TL;DR

This study found that 1.5% of elderly people in Russia reported lifetime epilepsy symptoms, with factors like neck pain and anemia being associated.

## Contribution

The study identifies novel associations between self-reported epilepsy symptoms and factors like neck pain and anemia in an elderly Russian population.

## Key findings

- Self-reported lifetime epilepsy symptoms were reported by 1.5% of participants.
- Neck pain, iron deficiency anemia, and unconsciousness were positively associated with epilepsy symptoms.
- Alcohol consumption was negatively associated with epilepsy symptoms.

## Abstract

The study aimed to explore the prevalence of self-reported lifetime epilepsy symptoms (SLESs) and associated factors among an elderly population in Russia.

The population-based Ural Very Old Study (UVOS) was conducted in Bashkortostan, Russia. Of 1882 eligible inhabitants aged 85 + years, 1,526 (81.1%) participated, including 389 (25.5%) men and 1,137 (74.5%) women. The participants underwent a detailed medical examination and interview, during which a history of epileptic attacks was assessed using standardized questions.

Of the 1,526 participants, 1,523 (99.9%), with a mean age of 88.8 ± 2.9 years (range: 85.0–103.1 years), provided information on epilepsy-related questions during the interview. A history of self-reported lifetime epilepsy symptoms was found in 23 individuals (1.5%; 95% confidence interval (CI): 0.90, 2.12), including 4 (17%) men. The mean age of these individuals was 89.2 ± 3.8 years (85.0–103.1 years). In a multivariable analysis, a higher prevalence of self-reported lifetime epilepsy symptoms was associated with a higher prevalence of neck pain (OR:3.53;95%CI:1.35,9,22;p = 0.01), iron deficiency-related anemia (OR: 5.68; 95%CI: 1.66, 19.5; p = 0.006), and unconsciousness (OR: 7.5295%CI: 2.69, 21.0; p < 0.001), as well as with a lower prevalence of any alcohol consumption (OR:0.14;95%CI:0.05, 0.44;p < 0.001) and a higher erythrocyte sedimentation rate (OR: 1.04; 95%CI: 1.01, 1.08; p = 0.01). It was not associated with level of education (p = 0.67), sex (p = 0.54), region of habitation (p = 0.18), Russian versus non-Russian ethnic background (p = 0.48), prevalence of diabetes (p = 0.93), or stages of arterial hypertension (p = 0.85).

Self-reported lifetime epilepsy symptoms, experienced at any period of life and assessed using a questionnaire with standardized questions, were reported by 23 of 1,523 participants (1.5%) in this very old population in Bashkortostan. The prevalence was independent of sex, educational level, ethnic background, rural versus urban region of habitation, diabetes mellitus, and arterial hypertension.

## Linked entities

- **Diseases:** epilepsy (MONDO:0005027), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** HMGB1 (high mobility group box 1) [NCBI Gene 3146] {aka HMG-1, HMG1, HMG3, SBP-1}
- **Diseases:** hearing loss (MESH:D034381), neurological disorders (MESH:D009461), epileptic fits (MESH:D012640), metabolic (MESH:D008659), hematological deficiencies (MESH:D019337), iron deficiency (MESH:D000090463), neck pain (MESH:D019547), chronic obstructive pulmonary disease (MESH:D029424), secondary epilepsy (MESH:D000068376), diarrhea (MESH:D003967), Stroke (MESH:D020521), SLESs (MESH:D012652), unconsciousness (MESH:D014474), Alzheimer's disease (MESH:D000544), diabetes (MESH:D003920), Huntington's disease (MESH:D006816), Idiopathic epilepsy (MESH:C562694), angina pectoris (MESH:D000787), central nervous system disorders (MESH:D002493), neuroinflammation (MESH:D000090862), injuries (MESH:D014947), inflammation (MESH:D007249), syncope (MESH:D013575), skin disease (MESH:D012871), Neuropathy (MESH:D009422), cognitive function (MESH:D003072), musculoskeletal (MESH:D009140), Depression (MESH:D003866), epileptic attacks (MESH:D009203), anemia (MESH:D000740), arthritis (MESH:D001168), Epilepsy (MESH:D004827), amyotrophic lateral sclerosis (MESH:D000690), hypertension (MESH:D006973), died (MESH:D003643), back pain (MESH:D001416)
- **Chemicals:** iron (MESH:D007501), alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12920221/full.md

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Source: https://tomesphere.com/paper/PMC12920221