# A Heuristic Approach to Analysis of the Genetic Susceptibility Profile in Patients Affected by Airway Allergies

**Authors:** Domenico Lio, Gabriele Di Lorenzo, Ignazio Brusca, Letizia Scola, Chiara Bellia, Simona La Piana, Maria Barrale, Manuela Bova, Loredana Vaccarino, Giusi Irma Forte, Giovanni Pilato

PMC · DOI: 10.3390/genes15081105 · Genes · 2024-08-22

## TL;DR

This paper explores genetic factors in airway allergies using a heuristic method to identify combinations of gene variations that may increase allergy risk.

## Contribution

The study introduces a heuristic approach using association rule mining to uncover complex genetic patterns linked to allergic susceptibility.

## Key findings

- Certain genotypes of IL-6, IL-10RB, IL-13, CD23, and Klotho genes are identified as potential risk factors for allergies.
- Ten genotype combination patterns were found to be associated with susceptibility to allergies using market basket analysis.
- The heuristic approach is suggested as a useful tool for identifying predictive and therapeutic molecular patterns in allergies.

## Abstract

Allergic respiratory diseases such as asthma might be considered multifactorial diseases, having a complex pathogenesis that involves environmental factors and the activation of a large set of immune response pathways and mechanisms. In addition, variations in genetic background seem to play a central role. The method developed for the analysis of the complexities, as association rule mining, nowadays may be applied to different research areas including genetic and biological complexities such as atopic airway diseases to identify complex genetic or biological markers and enlighten new diagnostic and therapeutic targets. A total of 308 allergic patients and 205 controls were typed for 13 single nucleotide polymorphisms (SNPs) of cytokine and receptors genes involved in type 1 and type 2 inflammatory response (IL-4 rs2243250 C/T, IL-4R rs1801275A/G, IL-6 rs1800795 G/C, IL-10 rs1800872 A/C and rs1800896 A/G, IL-10RB rs2834167A/G, IL-13 rs1800925 C/T, IL-18 rs187238G/C, IFNγ rs 24030561A/T and IFNγR2 rs2834213G/A), the rs2228137C/T of CD23 receptor gene and rs577912C/T and rs564481C/T of Klotho genes, using KASPar SNP genotyping method. Clinical and laboratory data of patients were analyzed by formal statistic tools and by a data-mining technique—market basket analysis—selecting a minimum threshold of 90% of rule confidence. Formal statistical analyses show that IL-6 rs1800795GG, IL-10RB rs2834167G positive genotypes, IL-13 rs1800925CC, CD23 rs2228137TT Klotho rs564481TT, might be risk factors for allergy. Applying the association rule methodology, we identify 10 genotype combination patterns associated with susceptibility to allergies. Together these data necessitate being confirmed in further studies, indicating that the heuristic approach might be a straightforward and useful tool to find predictive and diagnostic molecular patterns that might be also considered potential therapeutic targets in allergy.

## Linked entities

- **Genes:** IL4 (interleukin 4) [NCBI Gene 3565], IL4R (interleukin 4 receptor) [NCBI Gene 3566], IL6 (interleukin 6) [NCBI Gene 3569], IL10 (interleukin 10) [NCBI Gene 3586], IL10RB (interleukin 10 receptor subunit beta) [NCBI Gene 3588], IL13 (interleukin 13) [NCBI Gene 3596], IL18 (interleukin 18) [NCBI Gene 3606], IFNG (interferon gamma) [NCBI Gene 3458], IFNGR2 (interferon gamma receptor 2) [NCBI Gene 3460], FCER2 (Fc epsilon receptor II) [NCBI Gene 2208], CG9701 (uncharacterized protein) [NCBI Gene 39872]
- **Diseases:** asthma (MONDO:0004979), allergy (MONDO:0005271)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IL4R (interleukin 4 receptor) [NCBI Gene 3566] {aka CD124, IL-4RA, IL4RA}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, FCER2 (Fc epsilon receptor II) [NCBI Gene 2208] {aka BLAST-2, CD23, CD23A, CLEC4J, FCE2, FCErII}, IFNGR2 (interferon gamma receptor 2) [NCBI Gene 3460] {aka AF-1, IFGR2, IFNGT1, IMD28}, IL10RB (interleukin 10 receptor subunit beta) [NCBI Gene 3588] {aka CDW210B, CRF2-4, CRFB4, D21S58, D21S66, IBD25}, KL (klotho) [NCBI Gene 9365] {aka HFTC3, KLA}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}
- **Diseases:** atopic airway diseases (MESH:D029424), Allergies (MESH:D004342), asthma (MESH:D001249), Allergic respiratory diseases (MESH:D012130), type 1 and type 2 inflammatory (MESH:D003924)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs 24030561, rs2834167, rs1800872, G/C, rs1800925, rs2228137, rs564481, rs187238, rs1801275, rs1800795, rs2834213, A/T, rs577912, G/A, rs1800896, C/T, rs2243250, A/C, A/G

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11353610/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC11353610/full.md

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Source: https://tomesphere.com/paper/PMC11353610