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DOI 10.1007/s10286-017-0444-4

Медицинская библиотека · Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2017

Heart-rate response to alpha2-adrenergic receptor antagonism by antipsychotics.

Kim David D, Lang Donna J, Warburton Darren E R, Woodward Melissa L, White Randall F, Barr Alasdair M, Honer William G, Procyshyn Ric M

Клиническое исследованиеСтатьяПеревод в очереди

Аннотация

PURPOSE: To explore the relationship between antipsychotic-associated antagonism of alpha2-adrenergic receptors and resting heart rate in individuals with schizophrenia.

METHODS

Thirty-one inpatients treated with antipsychotics were included in this exploratory analysis. Antipsychotic doses were converted to haloperidol equivalents for alpha2-adrenergic receptor antagonism. Resting heart rate was measured with the patient in the seated upright posture.

RESULTS

After controlling for confounding variables, the relationship between alpha2-adrenergic receptor antagonism and resting heart rate demonstrated a positive linear effect (P = 0.002) as well as a nonlinear effect that accounted for an additional 14% of the variability in resting heart rate (P = 0.005).

CONCLUSION

The observed inverted-U relationship between alpha2-adrenergic receptor antagonism and resting heart rate can possibly be attributed to an altered response of beta1-adrenergic receptors to increased norepinephrine release. Further investigations are required to confirm this exploratory finding, taking into account additional variables that include other receptors which either directly or indirectly influence heart rate. CLINICALTRIALS.

GOV IDENTIFIER: NCT01392885.

Для цитирования: Kim David D, Lang Donna J, Warburton Darren E R, Woodward Melissa L, White Randall F, Barr Alasdair M, Honer William G, Procyshyn Ric M. Heart-rate response to alpha2-adrenergic receptor antagonism by antipsychotics.. Clinical autonomic research : official journal of the Clinical Autonomic Research Society. 2017. DOI: 10.1007/s10286-017-0444-4.

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