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In the June issue of
In the June issue of Anesthesiology, researchers take aim at identifying genetic risk factors for sepsis – a leading cause of death for critically ill patients.
Genetic makeup has been identified as a key factor leading to the development of sepsis, a systemic inflammatory reaction that occurs during infection. Sepsis is considered severe when associated with organ dysfunction.
In humans, multiple copies of some genes can occur and these multiple copies vary greatly among individuals. Large scale copy number variations (CNVs) were recently identified throughout the entire human genome. CNVs affect gene expression and patient response characteristics by altering the number of copies of a gene present in a cell or nucleus. This affect on gene dosage can cause disease or present risk to the development of complex traits.
“CNVs constitute a major source of inter-individual genetic variation and might represent a major factor in the cause of complex traits such as response to infection and sepsis,” said XiangMing Fang, MD, of the Department of Anesthesiology, the First Affiliated Hospital, School of Medicine at Zhejian University in Hangzhou, China. “It is believed that detection of both CNVs and conventional genetic marker single nucleotide polymorphisms (SNPs) will provide deep insight into the genetic and immune mechanism underlying sepsis.”
Another consideration for genetic risk of sepsis involves one group of white blood cells, neutrophils. They are the body’s first line of defense against infection, migrating to an infection site to engulf and kill microbes. Due to neutrophil activation during sepsis, the levels of neutrophil peptides 1-3 are greatly increased in the blood of patients with the disease., These peptides play an important role in infectious and inflammatory diseases.
The genes encoding human neutrophil peptides 1-3, (DEFA1/DEFA3) exhibit CNVs. Dr. Fang and colleagues set out to determine whether DEFA1/DEFA3 CNVs was related to patient susceptibility to infection induced by complications such as severe sepsis.
The team found that the genotype DEFA1/DEFA3 with >8 copies was more frequent in patients with severe sepsis than in the control group (55.9 percent vs. 31.3 percent). The established association between the genotype and severe sepsis was replicated in the second age and gender matched case controlled cohort.
Researchers concluded that DEFA1/DEFA3 is an important genetic component participating in the immune response to severe sepsis as a higher copy number of DEFA1/DEFA3 (>8 copies) is significantly associated with risk of severe sepsis.
“This study is the first to demonstrate that CNVs, within DEFA1/DEFA3 contribute significantly to susceptibility to severe sepsis,” said Fang. “This finding may help to identify patients at high risk for predisposition to severe sepsis so that preventive interventions and personalized therapy can be implemented.”