{"id":45678,"date":"2023-02-23T11:37:58","date_gmt":"2023-02-23T16:37:58","guid":{"rendered":"https:\/\/research.uga.edu\/news\/?p=45678"},"modified":"2023-11-02T11:55:21","modified_gmt":"2023-11-02T15:55:21","slug":"researchers-advance-knowledge-on-debilitating-genetic-disease","status":"publish","type":"post","link":"https:\/\/research.uga.edu\/news\/researchers-advance-knowledge-on-debilitating-genetic-disease\/","title":{"rendered":"Researchers advance knowledge on debilitating genetic disease"},"content":{"rendered":"

[vc_row][vc_column][vc_column_text el_class=”text-container first-paragraph”]<\/p>\n

A team of researchers at the University of Georgia has identified the source of several symptoms in patients suffering from familial dysautonomia (FD), a rare and debilitating genetic disease that primarily affects children. This new knowledge could lead to improved treatments to mitigate symptoms and improve the overall quality of life for patients.<\/p>\n

FD impairs the functioning of several nervous system branches simultaneously, limiting the ability of nerve cells throughout the body to work properly. Symptoms vary but typically emerge in early infancy as poor growth and feeding issues, then progress throughout a patient\u2019s lifetime to include developmental delays, frequent pneumonia and poor control of blood pressure, body temperature and breathing. As a result, FD patients typically have shorter life expectancies.<\/p>\n

Researchers hope that by identifying underlying causes of the disease, they can better inform medical interventions for FD, as well as similar conditions like cardiovascular disease, heart failure and stress-related disorders like anxiety.<\/p>\n

\u201cIn conducting this research, we hope to not only unlock answers about FD but trigger research into a whole haystack of diseases\u2014specifically, what causes them,\u201d said Nadja Zeltner, an assistant professor in UGA\u2019s Center for Molecular Medicine<\/a> and the project\u2019s principal investigator.<\/p>\n

\"Wu
Hsueh-Fu Wu, an advisee of Zeltner, is the first author of the publication in \u201cNature Communications.”<\/figcaption><\/figure>\n

These findings were published<\/a> in a recent issue of \u201cNature Communications,\u201d in which Zeltner\u2019s Ph.D. advisee Hsueh-Fu Wu served as first author.<\/p>\n

One particularly concerning aspect of FD is the \u201cdysautonomic crisis\u201d\u2014extreme episodes that frequently result in vomiting, severe shifts in heart rate and blood pressure, and personality changes. These events, long understudied, form the core of Zeltner\u2019s research.<\/p>\n

\u201cThe dysautonomic crisis is triggered by stress,\u201d Zeltner explained. \u201cPositive stress, negative stress\u2014 it doesn\u2019t matter. Just imagine a panic attack that doesn\u2019t really go away.\u201d<\/p>\n

The symptoms associated with these episodes are controlled by sympathetic neurons, the same nerves responsible for triggering fight-or-flight reactions. In her research, Zeltner used stem cells from FD patients that were converted into sympathetic nerve cells to better understand why these cells do not work and why they produce such severe symptoms in patients. This work yielded significant results that previously had not been demonstrated by research.<\/p>\n

\u201cResearchers originally thought that these neurons die and leave no trace behind,\u201d Zeltner said. \u201cBut we found that they\u2019re actually hyperactive. Nobody had shown that before.\u201d<\/p>\n

Hyperactivity is a stark departure from previous findings. It was determined that sympathetic neurons in FD patients cause such unpleasant symptoms because they activate tissues within the body to an excessive degree. This not only helps to explain why patients react the way they do to stressful events, but also helps unlock questions about potential treatments.<\/p>\n

In her study, Zeltner tested a series of drugs to see if they helped reduce hyperactivity associated with FD. This began with testing dexmedetomidine, which currently used for patients in dysautonomic crisis; the drug was determined to be effective precisely because it reduced the hyperactivity.<\/p>\n

\u201cThat was really cool, to see how this drug is tied to effectiveness,\u201d Zeltner said. \u201cBecause of this research, we can now help by explaining more about the mechanism behind this drug.\u201d<\/p>\n

Zeltner then studied a number of other drugs known to reduce hyperactivity, several of which also proved successful in mitigating hyperactivity associated with FD. This potentially exciting development might shed new light on how to control symptoms in patients, but Zeltner warned that it\u2019s too early to know how this research might impact treatment.<\/p>\n

\u201cWe\u2019re pretty far from being able to give new drugs to patients, for example,\u201d Zeltner said. \u201cBut it\u2019s a good start. What this research has done is provide a platform for previously unconsidered drugs to be tested, and that\u2019s a really valuable tool.\u201d<\/p>\n

This research also has the potential to unlock answers about a wide range of stress-induced disorders, ranging from hypertension to heart failure. That\u2019s because understanding the stress mechanisms in FD patients, especially in relation to the sympathetic nervous system, provides a strong model for understanding the effects of stress upon people in a variety of conditions.<\/p>\n

\u201cStress is a very omnipresent problem in our daily lives,\u201d Wu said. \u201cHopefully we can apply this knowledge from this model system to other stress-related metabolic diseases. That\u2019s the goal.\u201d<\/p>\n

These findings were published in the November 2022 edition of \u201cNature Communications.\u201d Zeltner and Wu were joined by seven other researchers, five of whom work for the University of Georgia: Wenxin Yu and Hong-Xiang Liu of UGA\u2019s Regenerative Bioscience Center; Chia-Wei Huang and Gerald Hart of UGA\u2019s Complex Carbohydrate Research Center; and Kenyi Saito-Diaz, of UGA\u2019s Center for Molecular Medicine. Joseph Carey and Frances Lefcort of Montana State University also helped conduct the research.<\/p>\n

[\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

[vc_row][vc_column][vc_column_text el_class=”text-container first-paragraph”] A team of researchers at the University of Georgia has identified the source of several symptoms in patients suffering from familial dysautonomia (FD), a rare and debilitating genetic disease that primarily affects children. This new knowledge could lead to improved treatments to mitigate symptoms and improve the overall quality of life for … <\/p>\n

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