Key result
SOD1 Del/Del genotype linked to ~133% higher rate of early bipolar onset without altering overall risk.
Why the study?
Bipolar disorder type 1 is associated with oxidative stress, and the role of a functional 50-bp Ins/Del polymorphism in the SOD1 gene promoter in BPD risk and age of onset was unclear.
Is the SOD1 50-bp Ins/Del polymorphism associated with the risk and age of onset of Bipolar disorder type 1?
Case-Control (n=452)
Is the SOD1 50-bp Ins/Del polymorphism associated with the risk and age of onset of Bipolar disorder type 1?
The SOD1 50-bp Ins/Del polymorphism is associated with an earlier age of onset of bipolar disorder type 1, though not with overall disease risk.
SOD1 Ins/Del polymorphism shows no BPD risk association; leaves open its potential role in age of onset.
Bipolar disorder type 1 (BPD) is a chronic psychiatric illness and is associated with oxidative stress. Superoxide dismutase-1 (SOD1; OMIM: 147450) metabolizes highly reactive and more dangerous superoxide radicals into less reactive molecules. A functional 50-bp insertion/deletion (Ins/Del) polymorphism in the promoter region of the gene has been reported. The primary aim of the current case-control study was to explore whether the SOD1 Ins/Del polymorphism associated with the risk of BPD. A secondary aim was to investigate the association between the study polymorphism and age of onset of BPD. The present case-control study was performed in Shiraz (southern Iran) on 228 BPD and 224 healthy blood donor controls. The genotypes of the SOD1 Ins/Del polymorphism were determined by polymerase chain reaction. There was no significant association between the genotypes of Ins/Del polymorphism and the risk of BPD. Using Cox proportional hazards regression model, after adjustment for family history of BPD, revealed a significant association between the SOD1 Ins/Del polymorphism and age of onset. The age of onset was significantly lower for the Del/Del genotype than the 'Ins/Ins + Ins/Del' genotypes (hazard ratio = 2.33, 95%CI: 1.08-5.02, p = .030). Our present findings revealed that although the SOD1 Ins/Del polymorphism was not associated with the risk of BPD, it was significantly associated with age of onset of BPD.
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Kordestanian et al. (2017) conducted a case-control in Bipolar disorder type 1 (n=452). SOD1 50-bp Ins/Del polymorphism vs. Healthy blood donor controls was evaluated on Risk of bipolar disorder type 1. The SOD1 Ins/Del polymorphism was not associated with bipolar disorder type 1 risk, but the Del/Del genotype was associated with a lower age of onset (HR 2.33; 95% CI 1.08-5.02; p=0.030).
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