TY - JOUR
T1 - Low growth hormone secretion associated with post-acute sequelae SARS-CoV-2 infection (PASC) neurologic symptoms
T2 - A case-control pilot study
AU - Wright, Traver J.
AU - Pyles, Richard B.
AU - Sheffield-Moore, Melinda
AU - Deer, Rachel
AU - Randolph, Kathleen M.
AU - McGovern, Kristen A.
AU - Danesi, Christopher P.
AU - Gilkison, Charles R.
AU - Ward, Weston W.
AU - Vargas, Jayson A.
AU - Armstrong, Peyton A.
AU - Lindsay, Sarah E.
AU - Zaidan, Mohammed F.
AU - Seashore, Justin
AU - Wexler, Tamara L.
AU - Masel, Brent E.
AU - Urban, Randall J.
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2024/1/1
Y1 - 2024/1/1
N2 - Objective: To determine if patients that develop lingering neurologic symptoms of fatigue and “brain fog” after initial recovery from coronavirus disease 2019 (COVID-19) have persistent low growth hormone (GH) secretion as seen in other conditions with similar symptom etiology. Design: In this case-control observational pilot study, patients reporting lingering neurologic post-acute sequelae of SARS-CoV-2 (PASC, n = 10) symptoms at least 6 months after initial infection were compared to patients that recovered from COVID-19 without lingering symptoms (non-PASC, n = 13). We compared basic blood chemistry and select metabolites, lipids, hormones, inflammatory markers, and vitamins between groups. PASC and non-PASC subjects were tested for neurocognition and GH secretion, and given questionnaires to assess symptom severity. PASC subjects were also tested for glucose tolerance and adrenal function. Results: PASC subjects reported significantly worse fatigue, sleep quality, depression, quality of life, and gastrointestinal discomfort compared to non-PASC. Although PASC subjects self-reported poor mental resilience, cognitive testing did not reveal significant differences between groups. Neurologic PASC symptoms were not linked to inflammatory markers or adrenal insufficiency, but were associated with reduced growth hormone secretion. Conclusions: Neurologic PASC symptoms are associated with gastrointestinal discomfort and persistent disruption of GH secretion following recovery from acute COVID-19. (www.clinicaltrials.gov;
AB - Objective: To determine if patients that develop lingering neurologic symptoms of fatigue and “brain fog” after initial recovery from coronavirus disease 2019 (COVID-19) have persistent low growth hormone (GH) secretion as seen in other conditions with similar symptom etiology. Design: In this case-control observational pilot study, patients reporting lingering neurologic post-acute sequelae of SARS-CoV-2 (PASC, n = 10) symptoms at least 6 months after initial infection were compared to patients that recovered from COVID-19 without lingering symptoms (non-PASC, n = 13). We compared basic blood chemistry and select metabolites, lipids, hormones, inflammatory markers, and vitamins between groups. PASC and non-PASC subjects were tested for neurocognition and GH secretion, and given questionnaires to assess symptom severity. PASC subjects were also tested for glucose tolerance and adrenal function. Results: PASC subjects reported significantly worse fatigue, sleep quality, depression, quality of life, and gastrointestinal discomfort compared to non-PASC. Although PASC subjects self-reported poor mental resilience, cognitive testing did not reveal significant differences between groups. Neurologic PASC symptoms were not linked to inflammatory markers or adrenal insufficiency, but were associated with reduced growth hormone secretion. Conclusions: Neurologic PASC symptoms are associated with gastrointestinal discomfort and persistent disruption of GH secretion following recovery from acute COVID-19. (www.clinicaltrials.gov;
KW - Biomarkers
KW - Cognition
KW - Depression
KW - Fatigue
KW - Gastrointestinal
KW - Growth hormone
KW - Long COVID
KW - PASC
KW - Quality of life
KW - SARS-CoV-2
KW - Sleep
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U2 - 10.1016/j.mce.2023.112071
DO - 10.1016/j.mce.2023.112071
M3 - Article
C2 - 37816478
AN - SCOPUS:85173842728
SN - 0303-7207
VL - 579
JO - Molecular and Cellular Endocrinology
JF - Molecular and Cellular Endocrinology
M1 - 112071
ER -