# Genetic, Sociodemographic and Clinical Determinants of COVID-19 Severity in the Republic of Srpska: Exploring Potential Links with Neanderthal-Derived Variants

**Authors:** Milena Dubravac Tanasković, Biljana Mijović, Jovan Kulić, Bojan Joksimović, Kristina Drašković-Mališ, Srđan Mašić, Jelena Vladičić-Mašić, Ljiljana Krsmanović, Danijela Radulović, Nikolina Elez-Burnjaković

PMC · DOI: 10.3390/biomedicines14020478 · Biomedicines · 2026-02-22

## TL;DR

This study explores how Neanderthal-derived genetic variants and sociodemographic factors may influence the severity of COVID-19 in the Republic of Srpska.

## Contribution

The study identifies a potential link between the LZTFL1 AG genotype and increased hospitalization risk for COVID-19.

## Key findings

- Hospitalized patients had a higher frequency of the LZTFL1 AG genotype compared to non-hospitalized individuals.
- Carriers of the LZTFL1 AG genotype had a higher chance of hospitalization compared to AA carriers.
- Combined CT (OAS3) and AG (LZTFL1) genotypes were more common in hospitalized patients, suggesting a synergistic effect.

## Abstract

Background/Objectives: COVID-19 severity is influenced by a complex interplay between host, viral, and environmental factors. Emerging evidence suggests that Neanderthal-derived genetic variants may influence the progression and severity of SARS-CoV-2 infection. This study aimed to evaluate the association between selected Neanderthal-derived variants and COVID-19 severity in the population of the Republic of Srpska, considering relevant clinical, sociodemographic, and lifestyle factors. Methods: This multicentric cross-sectional study included 402 participants, classified as healthy or SARS-CoV-2-positive individuals. A total of 378 COVID-19-positive participants were further stratified according to disease severity and hospitalization status. All individuals were genotyped for the Neanderthal-derived OAS3 rs1156361 (C/T) and LZTFL1 rs35044562 (A/G) variants. Detailed sociodemographic, clinical, and lifestyle data were also collected. Results: A higher frequency of the LZTFL1 rs35044562 AG genotype was observed among hospitalized patients compared with non-hospitalized individuals (36.8% vs. 20.9%; p = 0.005), while the AA genotype was more prevalent among non-hospitalized patients (77.3% vs. 63.2%, p = 0.015). Multivariable logistic analysis showed that carriers of the LZTFL1 AG genotype had a higher chance of hospitalization compared to AA carriers (adjusted OR = 1.372, 95% CI = 0.763–6.383, and p = 0.021). Hospitalized patients more frequently carried the combined CT (OAS3) and AG (LZTFL1) genotypes, supporting a potential synergistic effect. Several sociodemographic factors, including age, sex, education, employment, and urban residence, were also associated with COVID-19 severity, while no significant associations were observed in allele-based analyses. Conclusions: LZTFL1 gene polymorphisms may influence COVID-19 severity, with heterozygote-specific and combined risk effects observed. These preliminary findings are exploratory and require validation in larger cohorts, but may guide future studies and targeted interventions in high-risk groups.

## Linked entities

- **Genes:** OAS3 (2'-5'-oligoadenylate synthetase 3) [NCBI Gene 4940], LZTFL1 (leucine zipper transcription factor like 1) [NCBI Gene 54585]
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** CXCR6 (C-X-C motif chemokine receptor 6) [NCBI Gene 10663] {aka BONZO, CD186, CDw186, STRL33, TYMSTR}, CCR9 (C-C motif chemokine receptor 9) [NCBI Gene 10803] {aka CC-CKR-9, CDw199, GPR-9-6, GPR28}, XCR1 (X-C motif chemokine receptor 1) [NCBI Gene 2829] {aka CCXCR1, GPR5}, SLC6A20 (solute carrier family 6 member 20) [NCBI Gene 54716] {aka IMINO, SIT1, XT3, Xtrp3}, SMOC1 (SPARC related modular calcium binding 1) [NCBI Gene 64093] {aka OAS}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, RNASEL (ribonuclease L) [NCBI Gene 6041] {aka PRCA1, RNS4}, FYCO1 (FYVE and coiled-coil domain autophagy adaptor 1) [NCBI Gene 79443] {aka CATC2, CTRCT18, RUFY3, ZFYVE7}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, OAS1 (2'-5'-oligoadenylate synthetase 1) [NCBI Gene 4938] {aka E18/E16, IFI-4, IMD100, OIAS, OIASI}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, OAS3 (2'-5'-oligoadenylate synthetase 3) [NCBI Gene 4940] {aka p100, p100OAS}, TMPRSS2 (transmembrane serine protease 2) [NCBI Gene 7113] {aka PRSS10}, LZTFL1 (leucine zipper transcription factor like 1) [NCBI Gene 54585] {aka BBS17}, OAS2 (2'-5'-oligoadenylate synthetase 2) [NCBI Gene 4939] {aka AIAISD2}
- **Diseases:** thromboembolic (MESH:D013923), hypercholesterolemia (MESH:D006937), cerebrovascular diseases (MESH:D002561), cardiovascular disease (MESH:D002318), CKD (MESH:D012080), infected (MESH:D007239), myocardial infarction (MESH:D009203), COVID-19 (MESH:D000086382), deaths (MESH:D003643), hypertension (MESH:D006973), viral (MESH:D014777), acute respiratory distress (MESH:D012128), COPD (MESH:D029424), pneumonia (MESH:D011014), respiratory compromise (MESH:D012131), smoking (MESH:D015208), obesity (MESH:D009765), chronic kidney diseases (MESH:D051436), lung cancer (MESH:D008175), tumor (MESH:D009369), diabetes (MESH:D003920), inflammation (MESH:D007249), chronic liver disease (MESH:D008107), injury to (MESH:D014947), diseases (MESH:D004194)
- **Chemicals:** 2'-5'-oligoadenylates (MESH:C023505), ATP (MESH:D000255), EDTA (MESH:D004492)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]
- **Mutations:** rs67959919, rs10774671, A/G, rs10735079, rs11385942, rs73064425, rs1156361

## Full text

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## References

65 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937615/full.md

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Source: https://tomesphere.com/paper/PMC12937615