rs1800872 — IL10 -592 C>A

IL-10 Production — Cardiovascular Anti-Inflammatory Control

Interleukin-10 (IL-10) is the body's master anti-inflammatory cytokine¹¹ the body's master anti-inflammatory cytokine
IL-10 suppresses production of pro-inflammatory cytokines like TNF-α, IL-6, and IL-1β, acting as a critical brake on immune responses to prevent excessive inflammation. The IL10 gene on chromosome 1²² chromosome 1
Located at 1q31-32, position 206,773,062 encodes this regulatory cytokine. The -592 C>A polymorphism (rs1800872) sits in the promoter region, functioning as a dimmer switch that determines how much IL-10 your cells produce when inflammation begins. Unlike rs1800896 (IL10 -1082), which is already documented in GoodGenes' immune-gut category, rs1800872 provides additional resolution on the IL-10 haplotype and captures distinct cardiovascular and metabolic inflammation angles.

The Mechanism

The -592 position is part of a highly polymorphic promoter region³³ highly polymorphic promoter region
The three main IL10 promoter SNPs (-1082, -819, -592) exhibit strong linkage disequilibrium and form distinct haplotypes that forms three predominant haplotypes controlling IL-10 transcription: GCC (high producer), ACC (intermediate), and ATA (low producer). The A allele at -592 is a component of the ATA haplotype⁴⁴ ATA haplotype
Associated with 2-4 fold reduction in IL-10 transcription, which causes considerably reduced promoter function and decreased IL-10 gene expression. The C-to-A exchange at position -592 disrupts transcription factor binding⁵⁵ disrupts transcription factor binding
Affects binding sites that regulate how actively the gene is transcribed into mRNA, leading to lower IL-10 production in response to inflammatory stimuli.

The functional impact creates a paradoxical situation: higher IL-10 production generally suppresses inflammation⁶⁶ higher IL-10 production generally suppresses inflammation
IL-10 downregulates synthesis of IL-1, IL-6, and TNF-α, which should be protective. However, in cardiovascular contexts, the AA genotype (low IL-10 producer) shows mixed associations—in some studies linked with increased atherosclerosis and coronary artery disease risk⁷⁷ increased atherosclerosis and coronary artery disease risk
Chinese population study found A allele associated with CAD, OR varies by population, yet paradoxically also associated with elevated HDL cholesterol, reduced intima-media thickness, and less peripheral artery stenosis⁸⁸ elevated HDL cholesterol, reduced intima-media thickness, and less peripheral artery stenosis
Russian study of acute coronary syndrome patients in certain populations. This complexity reflects IL-10's dual role: too little allows unchecked inflammation, but chronic elevation can signal uncontrolled inflammatory disease.

The Evidence

Cancer protection⁹⁹ Cancer protection
Meta-analysis of 70 studies encompassing 16,785 cases and 19,713 controls provides the strongest evidence: the AA genotype confers moderately decreased cancer risk (OR 0.90, 95% CI 0.83-0.98) compared to CC. The protective effect is particularly strong in smoking-related cancers (OR 0.77) and Asian populations (OR 0.79)¹⁰¹⁰ smoking-related cancers (OR 0.77) and Asian populations (OR 0.79). The mechanism likely involves the balance between anti-tumor immunity (requires some inflammation to clear cancer cells) versus chronic inflammation (which promotes tumorigenesis). Lower IL-10 production in AA carriers may allow more effective immune surveillance of pre-malignant cells.

Cardiovascular associations are more nuanced. A Chinese case-control study¹¹¹¹ Chinese case-control study
326 CAD patients vs. 248 controls found the A allele associated with increased coronary artery disease risk, with AA genotype carriers showing higher risk of >50% stenosis. Yet a Russian study¹²¹² Russian study
220 acute coronary syndrome patients found AA genotype carriers had elevated HDL cholesterol, reduced carotid intima-media thickness, lower frequency of peripheral artery stenosis, and—critically—increased IL-10 production despite the functional data suggesting the opposite. This paradox may reflect compensatory upregulation in the setting of active disease or population-specific genetic backgrounds.

The type 2 diabetes association is clearer. A North Indian study¹³¹³ North Indian study
260 T2DM patients vs. 280 controls found diabetes patients carried significantly more A alleles at -592 (25.6% vs. controls, P < 0.001). The mechanism involves chronic low-grade inflammation¹⁴¹⁴ mechanism involves chronic low-grade inflammation
Low serum IL-10 associated with increased T2DM and metabolic syndrome susceptibility—insufficient IL-10 allows persistent activation of inflammatory pathways that drive insulin resistance. Genotype-specific analysis showed CC genotype associated with T2DM¹⁵¹⁵ CC genotype associated with T2DM
Contrasting with AA's association with elevated HDL, while AA genotype paradoxically linked to both increased HDL and increased IL-10 in some cohorts.

In systemic lupus erythematosus¹⁶¹⁶ systemic lupus erythematosus
Iranian population study of 70 SLE patients vs. 211 controls, IL10 promoter polymorphisms including rs1800872 showed haplotype-dependent associations with disease activity and IL-10 levels. The complexity reflects IL-10's context-dependent effects: protective against inflammatory damage, yet high levels may indicate failure to resolve inflammation.

COVID-19 severity studies¹⁷¹⁷ COVID-19 severity studies
Brazilian and Egyptian cohort studies demonstrated that IL10 haplotypes (including -592) influence infection severity, with GCC haplotype homozygosity (high IL-10 producer) independently associated with severe disease (OR 2.77), possibly through excessive immunosuppression preventing viral clearance.

Practical Implications

Your genotype at -592 influences your baseline inflammatory regulation and may modulate risk for conditions ranging from cardiovascular disease to cancer to metabolic syndrome. The evidence suggests that IL-10 production exists in a Goldilocks zone—too little permits unchecked inflammation (atherosclerosis, insulin resistance), while chronic elevation signals inflammatory disease burden.

For cardiovascular health, the A allele shows population-specific and context-dependent effects. In some Asian populations it associates with increased CAD risk; in Eastern European populations with protective lipid profiles. The key insight: IL-10 is a marker of inflammatory tone, not a standalone risk factor. If you carry AA or AC genotypes, focus on anti-inflammatory dietary patterns¹⁸¹⁸ anti-inflammatory dietary patterns
Mediterranean diet consistently shows reductions in inflammatory markers including increased IL-10 rather than trying to "boost IL-10" in isolation.

For cancer risk, AA carriers show modest protection, particularly for smoking-related cancers. This isn't actionable in the sense of changing your genotype, but it underscores the importance of avoiding tobacco—the protective effect is stronger in smoking-exposed populations, suggesting lower IL-10 production may help clear pre-malignant cells in high-exposure settings.

For metabolic health, lower IL-10 production (AA genotype) may increase vulnerability to insulin resistance through chronic inflammatory signaling. Interventions that boost IL-10¹⁹¹⁹ Interventions that boost IL-10
Curcumin, omega-3s, Mediterranean diet, and mind-body practices increase IL-10 include omega-3 fatty acids (EPA/DHA), curcumin supplementation, vitamin D optimization, and mind-body practices like meditation that have been shown to increase IL-10 while reducing pro-inflammatory cytokines²⁰²⁰ increase IL-10 while reducing pro-inflammatory cytokines
Mindfulness retreat study showed significant IL-10 increases and IL-6/IL-8 reductions.

Interactions

The -592 variant (rs1800872) works in concert with two other IL10 promoter SNPs: -1082 A>G (rs1800896)²¹²¹ -1082 A>G (rs1800896)
Already documented in GoodGenes' immune-gut category and -819 C>T (rs1800871). These three variants exhibit strong linkage disequilibrium²²²² strong linkage disequilibrium
They travel together on chromosomes forming specific haplotype blocks and form haplotypes that determine IL-10 production capacity:

• GCC haplotype (high IL-10 producer): -1082G / -819C / -592C — associated with elevated IL-10 secretion, which generally suppresses inflammation but in COVID-19 studies linked to severe disease²³²³ linked to severe disease
  GCC homozygosity OR 2.77 for severe COVID, possibly through excessive immunosuppression

• ATA haplotype (low IL-10 producer): -1082A / -819T / -592A — associated with 2-4 fold reduced IL-10 transcription, linked to increased inflammatory disease susceptibility²⁴²⁴ linked to increased inflammatory disease susceptibility
  Low IL-10 producer haplotype in multiple autoimmune and inflammatory conditions but potential cancer protection

• ACC haplotype (intermediate): -1082A / -819C / -592C — intermediate IL-10 production

Understanding your full IL-10 haplotype requires knowing all three positions. If you're AA at -592, you likely carry at least one copy of the low-producer ATA haplotype, particularly if you also carry AA at -1082 (rs1800896). The combined effect is stronger than either variant alone—haplotype analysis in Iranian SLE patients²⁵²⁵ Iranian SLE patients
Study of 70 patients vs. 211 controls showed haplotype associations with disease activity that weren't apparent from single-SNP analysis.

The interaction with environmental factors is critical. Mindfulness and stress reduction interventions²⁶²⁶ Mindfulness and stress reduction interventions
Meta-analysis of mind-body interventions across multiple inflammatory diseases significantly increase IL-10 production, potentially compensating for genetically low expression. Similarly, omega-3 supplementation²⁷²⁷ omega-3 supplementation
EPA specifically lowers TNF-α/IL-10 ratio and dietary patterns like the Mediterranean diet combined with curcumin²⁸²⁸ Mediterranean diet combined with curcumin
RCT in ulcerative colitis patients show synergistic effects on inflammatory markers including IL-10.