Cold treatment does not appear to protect preterm infants from disability or death caused by oxygen loss, according to NIH-funded study
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Updates every hour. Last Updated: 8-May-2025 09:09 ET (8-May-2025 13:09 GMT/UTC)
Lowering the body temperature of preterm infants (born at 33 to 35 weeks of pregnancy) with hypoxic ischemic encephalopathy (HIE)—a type of brain damage caused by oxygen loss—offers no benefits over standard care, according to a study funded by the National Institutes of Health (NIH). Previous studies of near-term and term infants (born after 36 weeks) with HIE found that this cooling treatment, which lowers body temperature to about 92 degrees Fahrenheit, significantly reduced the risk of death or disability by age 18 months (corrected for prematurity). However, the current findings show that such benefits are not observed for preterm infants with HIE. The authors noted that use of the cooling treatment in preterm infants has increased, despite little research on its effectiveness in this age group.
Researchers at The University of Texas MD Anderson Cancer Center have developed a novel antibody-toxin conjugate (ATC) designed to stimulate immune-mediated eradication of tumors. According to preclinical results published today in Nature Cancer, the new approach combined the benefits of more well-known antibody-drug conjugates (ADCs) with those of immunotherapies.
The study, which examined the relationship between childhood exposure to trauma and vascular dysfunction among more than 400 Black adults in Atlanta ages 30 to 70, found that women who experienced childhood trauma had a worse vascular function, a preclinical marker of heart disease, while men had none. In addition, the findings indicated that women may be more vulnerable to a larger cumulative stress burden, eliciting varying physiological stress responses. Childhood trauma in women can cause arterial stiffness, or an impaired artery function of the cardiovascular system, contributing to major cardiac events, such as stroke and heart attack. It also contributes to heart disease, high blood pressure, and a malfunctioning small blood vessel system, which could damage tissues in the kidneys or brain.