Literature DB >> 24423319

Absence of central circadian pacemaker abnormalities in humans with loss of function mutation in prokineticin 2.

Ravikumar Balasubramanian1, Daniel A Cohen, Elizabeth B Klerman, Duarte Pignatelli, Janet E Hall, Andrew A Dwyer, Charles A Czeisler, Nelly Pitteloud, William F Crowley.   

Abstract

CONTEXT: Loss of prokineticin 2 (PROK2) signaling in mice disrupts circadian rhythms, but the role of PROK2 signaling in the regulation of circadian rhythms in humans is undetermined.
OBJECTIVE: The aim of the study was to examine the circadian rhythms of humans with a complete loss-of-function PROK2 mutation using an inpatient constant routine (CR) protocol. DESIGN AND
SETTING: We conducted a case study in an academic medical center. SUBJECTS AND METHODS: Two siblings (one male and one female, ages 67 and 62 y, respectively) with isolated GnRH deficiency (IGD) due to a biallelic loss-of-function PROK2 mutation were studied using an inpatient CR protocol. Historical data from inpatient CR protocols conducted in healthy controls (ages 65-81 y) were used for comparison. MAIN OUTCOME MEASURES: We measured circadian phase markers (melatonin, cortisol, and core body temperature) and neurobehavioral performance (psychomotor vigilance task [PVT] and subjective alertness scale).
RESULTS: Circadian waveforms of melatonin and cortisol did not differ between the IGD participants with PROK2 mutation and controls. In both IGD participants, neurobehavioral testing with PVT showed disproportionate worsening of PVT lapses and median reaction time in the second half of the CR.
CONCLUSIONS: Humans with loss of PROK2 signaling lack abnormalities in circadian phase markers, indicating intact central circadian pacemaker activity in these patients. These results suggest that PROK2 signaling in humans is not required for central circadian pacemaker function. However, impaired PVT in the PROK2-null participants despite preserved endocrine rhythms suggests that PROK2 may transmit circadian timing information to some neurobehavioral neural networks.

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Year:  2014        PMID: 24423319      PMCID: PMC3942237          DOI: 10.1210/jc.2013-2096

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  31 in total

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Journal:  J Clin Endocrinol Metab       Date:  2009-12-18       Impact factor: 5.958

2.  Attenuated circadian rhythms in mice lacking the prokineticin 2 gene.

Authors:  Jia-Da Li; Wang-Ping Hu; Lisa Boehmer; Michelle Y Cheng; Alex G Lee; Alexander Jilek; Jerome M Siegel; Qun-Yong Zhou
Journal:  J Neurosci       Date:  2006-11-08       Impact factor: 6.167

3.  Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.

Authors:  Nelly Pitteloud; Chengkang Zhang; Duarte Pignatelli; Jia-Da Li; Taneli Raivio; Lindsay W Cole; Lacey Plummer; Elka E Jacobson-Dickman; Pamela L Mellon; Qun-Yong Zhou; William F Crowley
Journal:  Proc Natl Acad Sci U S A       Date:  2007-10-24       Impact factor: 11.205

4.  Prokineticin 2 depolarizes paraventricular nucleus magnocellular and parvocellular neurons.

Authors:  Erik A Yuill; Ted D Hoyda; Catharine C Ferri; Qun-Yong Zhou; Alastair V Ferguson
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Journal:  J Clin Endocrinol Metab       Date:  2008-06-17       Impact factor: 5.958

8.  Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.

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9.  Efferent projections of prokineticin 2 expressing neurons in the mouse suprachiasmatic nucleus.

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Journal:  PLoS One       Date:  2009-09-28       Impact factor: 3.240

10.  Network features of the mammalian circadian clock.

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  2 in total

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2.  Gonadal Cycle-Dependent Expression of Genes Encoding Peptide-, Growth Factor-, and Orphan G-Protein-Coupled Receptors in Gonadotropin- Releasing Hormone Neurons of Mice.

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  2 in total

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