First report on ACE I/D polymorphism and lymphoma susceptibility in Algeria: Clinical and genetic insights
DOI:
https://doi.org/10.2298/ABS250930029SKeywords:
Hodgkin lymphoma, non-Hodgkin lymphoma, ACE I/D polymorphism, risk factors, North AfricaAbstract
Paper description:
- Lymphomas are multifactorial cancers shaped by genetic, clinical, and lifestyle factors. Evidence from North African populations remains limited.
- A case-control study in Algeria, including 86 patients with Hodgkin or non-Hodgkin lymphomas and 110 matched healthy controls, with ACE I/D polymorphism genotyping was undertaken.
- Smoking and hypertension were significantly associated with increased lymphoma risk; cardiovascular disease and allergy showed inverse associations. The ACE ID genotype was underrepresented in non-Hodgkin subtypes.
- This study provides the first evidence from Algeria linking ACE I/D polymorphism to lymphoma risk, underscoring the contribution of both genetic and modifiable factors relevant to disease prevention and personalized management.
Abstract: Lymphomas represent a heterogeneous group of malignancies influenced by genetic, clinical, and lifestyle factors, but data from North African populations remain scarce. We conducted a case-control study including 86 patients with Hodgkin and non-Hodgkin lymphomas and 110 matched healthy controls from Algeria to evaluate the demographic, clinical, and genetic determinants of disease risk. Smoking (OR=2.06, 95% CI: 1.48-2.87) and hypertension (OR=3.99, 95% CI: 2.37-6.71) were independently associated with increased lymphoma risk, whereas cardiovascular disease (OR=0.30, 95% CI: 0.14-0.65) and allergies (OR=0.25, 95% CI: 0.15-0.40) showed inverse associations. Genetic analysis revealed that the ACE ID genotype was inversely associated with lymphoma (OR=0.18, 95% CI: 0.08-0.38), particularly for non-Hodgkin subtypes. These findings suggest that both modifiable lifestyle factors and genetic variation within the renin-angiotensin system may affect lymphoma risk in the Algerian population. The results represent preliminary, population-specific evidence that should be validated in larger multicenter studies.
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Copyright (c) 2025 Choubeila SALHI, Rania Laouar, Djalila Chellat, Yacine Benhizia, Karima Sifi, Mohamed Larbi Rezgoun

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