Key result
Longer T2DM duration is linked to ~212% greater DKD odds alongside the SHROOM3 genetic locus.
Why the study?
Risk factors and genetic predisposition to diabetic kidney disease in the Emirati population with type 2 diabetes mellitus have not yet been investigated.
What are the clinical and genetic risk factors for diabetic kidney disease in Emirati patients with type 2 diabetes?
Cross-Sectional (n=490)
What are the clinical and genetic risk factors for diabetic kidney disease in Emirati patients with type 2 diabetes?
In an Emirati population with T2DM, longer diabetes duration and specific genetic loci such as SHROOM3 are associated with diabetic kidney disease and altered renal function traits.
Answers are grounded in this paper and cite their sources.
SHROOM3 and other loci associate with DKD in Emiratis; extends genetic signals to Arab ancestry but leaves clinical utility open.
Objectives Within the Emirati population, risk factors and genetic predisposition to diabetic kidney disease (DKD) have not yet been investigated. The aim of this research was to determine potential clinical, laboratory and reported genetic loci as risk factors for DKD. Research design and methods Four hundred and ninety unrelated Emirati nationals with type 2 diabetes mellitus (T2DM) were recruited with and without DKD, and clinical and laboratory data were obtained. Following adjustments for possible confounders, a logistic regression model was developed to test the associations of 63 single nucleotide polymorphisms (SNPs) in 43 genetic loci with DKD (145 patients with DKD and 265 without DKD). Linear regression models, adjusted for age and gender, were then used to study the genetic associations of five renal function traits, including 83 SNPs with albumin-to-creatinine ratio, 92 SNPs with vitamin D (25-OH cholecalciferol), 288 SNPs with estimated glomerular filtration rate (eGFR), 363 SNPs with serum creatinine and 73 SNPs with blood urea. Results Patients with DKD, as compared with those without the disease, were mostly men (52%vs38% for controls), older (67vs59 years) and had significant rates of hypertension and dyslipidaemia. Furthermore, patients with DKD had T2DM for a longer duration of time (16vs10 years), which in an additive manner was the single factor that significantly contributed to the development of DKD (p=0.02, OR=3.12, 95% CI 1.21 to 8.02). Among the replicated associations of the genetic loci with different renal function traits, the most notable includedSHROOM3with levels of serum creatinine, eGFR and DKD (Padjusted=0.04, OR=1.46);CASR,GCandCYP2R1with vitamin D levels; as well asWDR72with serum creatinine and eGFR levels. Conclusions Associations were found between several genetic loci and risk markers for DKD, which may influence kidney function traits and DKD in a population of Arab ancestry.
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Osman et al. (2018) conducted a cross-sectional in Type 2 diabetes mellitus with and without diabetic kidney disease (n=490). Longer duration of T2DM vs. Shorter duration of T2DM was evaluated on Diabetic kidney disease (DKD) (OR 3.12, 95% CI 1.21-8.02, p=0.02). Longer duration of type 2 diabetes mellitus (OR 3.12; 95% CI 1.21-8.02) and the SHROOM3 genetic locus (OR 1.46) were significantly associated with diabetic kidney disease in Emirati nationals.
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