• Something wrong with this record ?

Chronobiologie, genetika a metabolický syndrom
[Chronobiology, genetics and metabolic syndrome]

Marta Garaulet, Juan A. Madrid

. 2009 ; 3 (3) : 65-72.

Language Czech Country Czech Republic

Document type Review

Circadian rhythms are such an innate part of our lives that we rarely pause to speculate why they even exist. Recently, some studies have suggested that the disruption of the circadian system may be causal for the manifestations of metabolic syndrome (MetS). This review summarizes the latest evidence of the existing interaction among chronobiology, genetics and MetS. RECENT FINDINGS: Shift work, sleep deprivation and bright light exposure at night are related to increased adiposity and prevalence of MetS. Animal models have revealed that mice with circadian locomotor output cycles kaput (clock) gene disruption are prone to develop a phenotype resembling MetS. Moreover, studies in humans have shown that clock genes are expressed in adipose tissue, and that both their levels of expression and their genetic variants correlate with different components of the MetS. Current studies are illustrating the particular role of different clock gene variants and their predicted haplotypes in MetS. SUMMARY: The circadian system has an important impact on metabolic disturbances and vice versa. Although the precise mechanism linking the MetS to chronodisruption is not well known, hypotheses point to the internal desynchronization between different circadian rhythms. The novelty of this area of research is contributing to the development of new and intriguing studies, particularly those focused on the association between different clock genes polymorphisms and MetS traits.

Chronobiology, genetics and metabolic syndrome

Bibliography, etc.

Lit.: 64

000      
00000naa 2200000 a 4500
001      
bmc09002163
003      
CZ-PrNML
005      
20111210152356.0
008      
091103s2009 xr e cze||
009      
AR
040    __
$a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
041    0_
$a cze $b eng
044    __
$a xr
100    1_
$a Garaulet, Marta
245    10
$a Chronobiologie, genetika a metabolický syndrom / $c Marta Garaulet, Juan A. Madrid
246    11
$a Chronobiology, genetics and metabolic syndrome
314    __
$a Department of Physiology, University of Murcia, Murcia garaulet@um.es
504    __
$a Lit.: 64
520    9_
$a Circadian rhythms are such an innate part of our lives that we rarely pause to speculate why they even exist. Recently, some studies have suggested that the disruption of the circadian system may be causal for the manifestations of metabolic syndrome (MetS). This review summarizes the latest evidence of the existing interaction among chronobiology, genetics and MetS. RECENT FINDINGS: Shift work, sleep deprivation and bright light exposure at night are related to increased adiposity and prevalence of MetS. Animal models have revealed that mice with circadian locomotor output cycles kaput (clock) gene disruption are prone to develop a phenotype resembling MetS. Moreover, studies in humans have shown that clock genes are expressed in adipose tissue, and that both their levels of expression and their genetic variants correlate with different components of the MetS. Current studies are illustrating the particular role of different clock gene variants and their predicted haplotypes in MetS. SUMMARY: The circadian system has an important impact on metabolic disturbances and vice versa. Although the precise mechanism linking the MetS to chronodisruption is not well known, hypotheses point to the internal desynchronization between different circadian rhythms. The novelty of this area of research is contributing to the development of new and intriguing studies, particularly those focused on the association between different clock genes polymorphisms and MetS traits.
650    _2
$a financování organizované $7 D005381
650    _2
$a zvířata $7 D000818
650    _2
$a cirkadiánní rytmus $x fyziologie $x genetika $7 D002940
650    _2
$a lidé $7 D006801
650    _2
$a metabolický syndrom $x etiologie $x genetika $7 D024821
650    _2
$a polymorfismus genetický $x genetika $7 D011110
650    _2
$a trans-aktivátory $x fyziologie $x genetika $7 D015534
655    _2
$a přehledy $7 D016454
700    1_
$a Madrid, Juan A.
773    0_
$w MED00156015 $t Current opinion in lipidology $g Roč. 3, č. 3 (2009), s. 65-72 $x 1802-372X
910    __
$a ABA008 $b B 2483 $c 129 $y 9
990    __
$a 20091103155417 $b ABA008
991    __
$a 20091103162014 $b ABA008
999    __
$a ok $b bmc $g 691333 $s 553231
BAS    __
$a 3
BMC    __
$a 2009 $b 3 $c 3 $d 65-72 $i 1802-372X $m Current Opinion in Lipidology $x MED00156015
LZP    __
$a 2009-34/mkme

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...