-
Something wrong with this record ?
Neuromedin beta: P73T polymorphism in overweight and obese subjects
J. Spálová, H. Zamrazilová, J. Vcelák, M. Vanková, P. Lukásová, M. Hill, K. Hlavatá, P. Srámková, M. Fried, B. Aldhoon, M. Kunesová, B. Bendlová, V. Hainer
Language English Country Czech Republic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NR7800
MZ0
CEP Register
NR7809
MZ0
CEP Register
Digital library NLK
Full text - Article
Full text - Část
Source
Source
NLK
Directory of Open Access Journals
from 1991
Free Medical Journals
from 1998
ProQuest Central
from 2005-01-01
Medline Complete (EBSCOhost)
from 2006-01-01
Nursing & Allied Health Database (ProQuest)
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 1998
- MeSH
- Patient Compliance MeSH
- Adult MeSH
- Energy Intake genetics MeSH
- Genotype MeSH
- Hunger physiology MeSH
- Weight Loss genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- Overweight genetics MeSH
- Follow-Up Studies MeSH
- Neurokinin B analogs & derivatives genetics MeSH
- Obesity genetics MeSH
- Pilot Projects MeSH
- Polymorphism, Genetic * MeSH
- Sex Factors MeSH
- Feeding Behavior physiology MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Neuromedin beta (NMB) is a member of the bombesin-like peptide family expressed in brain, gastrointestinal tract, pancreas, adrenals and adipose tissue. The aim of our study was to compare the frequency of P73T polymorphism in overweight and obese patients (37 men: age 50.6+/-11.7 years, BMI 41.1+/-7.8 kg/m(2); 255 women: age 49.0+/-11.9 years, BMI 37.9+/-6.8 kg/m(2)) with that of healthy normal weight subjects (51 men: age 28.2+/-7.1 years, BMI 22.3+/-2.0 kg/m(2); 104 women: age 29.1+/-9.1 years, BMI 21.5+/-1.9 kg/m(2)) and to investigate the polymorphism's influence on anthropometric, nutritional and psychobehavioral parameters in overweight/obese patients both at the baseline examination and at a control visit carried out 2.5 years later, regardless of the patient s compliance with the weight reduction program. No significant differences in the genotype distribution were demonstrated between normal weight and overweight/obese subjects. Male T allele non-carriers compared to T allele carriers had higher energy (p=0.009), protein (p=0.018) and fat (p=0.002) intakes and hunger score (p=0.015) at the beginning of treatment. Male T allele non-carriers had a more favorable response to weight management at the follow-up, as they exhibited a significant reduction in waist circumference, energy intake and depression score as well as a significant increase in dietary restraint. No significant differences between carriers and non-carriers were demonstrated in women at the baseline examination. Both female T allele carriers and non-carriers demonstrated similar significant changes in nutritional parameters and in restraint score at the follow-up. Nevertheless, only female non-carriers showed a significant decrease in the hunger score.
Clinical Centre ISCARE 1 5 F Prague Czech Republic
Department of Cardiology Institute for Clinical and Experimental Medicine Prague Czech Republic
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13034110
- 003
- CZ-PrNML
- 005
- 20151006120359.0
- 007
- ta
- 008
- 131021s2008 xr f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.931488 $2 doi
- 035 __
- $a (PubMed)18271693
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Spálová, Jana $u Institute of Endocrinology, Prague, Czech Republic $7 _AN053814
- 245 10
- $a Neuromedin beta: P73T polymorphism in overweight and obese subjects / $c J. Spálová, H. Zamrazilová, J. Vcelák, M. Vanková, P. Lukásová, M. Hill, K. Hlavatá, P. Srámková, M. Fried, B. Aldhoon, M. Kunesová, B. Bendlová, V. Hainer
- 520 9_
- $a Neuromedin beta (NMB) is a member of the bombesin-like peptide family expressed in brain, gastrointestinal tract, pancreas, adrenals and adipose tissue. The aim of our study was to compare the frequency of P73T polymorphism in overweight and obese patients (37 men: age 50.6+/-11.7 years, BMI 41.1+/-7.8 kg/m(2); 255 women: age 49.0+/-11.9 years, BMI 37.9+/-6.8 kg/m(2)) with that of healthy normal weight subjects (51 men: age 28.2+/-7.1 years, BMI 22.3+/-2.0 kg/m(2); 104 women: age 29.1+/-9.1 years, BMI 21.5+/-1.9 kg/m(2)) and to investigate the polymorphism's influence on anthropometric, nutritional and psychobehavioral parameters in overweight/obese patients both at the baseline examination and at a control visit carried out 2.5 years later, regardless of the patient s compliance with the weight reduction program. No significant differences in the genotype distribution were demonstrated between normal weight and overweight/obese subjects. Male T allele non-carriers compared to T allele carriers had higher energy (p=0.009), protein (p=0.018) and fat (p=0.002) intakes and hunger score (p=0.015) at the beginning of treatment. Male T allele non-carriers had a more favorable response to weight management at the follow-up, as they exhibited a significant reduction in waist circumference, energy intake and depression score as well as a significant increase in dietary restraint. No significant differences between carriers and non-carriers were demonstrated in women at the baseline examination. Both female T allele carriers and non-carriers demonstrated similar significant changes in nutritional parameters and in restraint score at the follow-up. Nevertheless, only female non-carriers showed a significant decrease in the hunger score.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a energetický příjem $x genetika $7 D002149
- 650 _2
- $a stravovací zvyklosti $x fyziologie $7 D005247
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a následné studie $7 D005500
- 650 _2
- $a genotyp $7 D005838
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a hlad $x fyziologie $7 D006815
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a neurokinin B $x analogy a deriváty $x genetika $7 D015287
- 650 _2
- $a obezita $x genetika $7 D009765
- 650 _2
- $a nadváha $x genetika $7 D050177
- 650 _2
- $a adherence pacienta $7 D010349
- 650 _2
- $a pilotní projekty $7 D010865
- 650 12
- $a polymorfismus genetický $7 D011110
- 650 _2
- $a sexuální faktory $7 D012737
- 650 _2
- $a hmotnostní úbytek $x genetika $7 D015431
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Zamrazilová, Hana $u Institute of Endocrinology, Prague, Czech Republic $7 xx0092178
- 700 1_
- $a Včelák, Josef, $u Institute of Endocrinology, Prague, Czech Republic $d 1971- $7 xx0107261
- 700 1_
- $a Vaňková, Markéta, $u Institute of Endocrinology, Prague, Czech Republic $d 1974- $7 xx0140642
- 700 1_
- $a Lukášová, Petra $u Institute of Endocrinology, Prague, Czech Republic $7 xx0078664
- 700 1_
- $a Hill, Martin, $u Institute of Endocrinology, Prague, Czech Republic $d 1962- $7 mzk2005304431
- 700 1_
- $a Hlavatá, Karolína, $u Institute of Endocrinology, Prague, Czech Republic $d 1978- $7 xx0059763
- 700 1_
- $a Šrámková, Petra, $u Clinical Centre ISCARE I.V.F., Prague, Czech Republic $d 1970- $7 xx0119617
- 700 1_
- $a Fried, Martin, $u Clinical Centre ISCARE I.V.F., Prague, Czech Republic $d 1956- $7 nlk20030142871
- 700 1_
- $a Aldhoon, Bashar $u Institute of Endocrinology, Prague, Czech Republic; Department of Cardiology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic $7 xx0073780
- 700 1_
- $a Kunešová, Marie, $u Institute of Endocrinology, Prague, Czech Republic $d 1951- $7 jn19990209456
- 700 1_
- $a Bendlová, Běla, $u Institute of Endocrinology, Prague, Czech Republic $d 1962- $7 jo20000074069
- 700 1_
- $a Hainer, Vojtěch, $u Institute of Endocrinology, Prague, Czech Republic $d 1944- $7 jn19990209207
- 773 0_
- $w MED00003824 $t Physiological research $x 0862-8408 $g Roč. 57,Suppl 1 (2008), s. S39-S48
- 773 0_
- $t From clinical to molecular endocrinology $x 0862-8408 $g Roč. 57,Suppl 1 (2008), s. S39-S48 $w MED00170142
- 856 41
- $u http://www.biomed.cas.cz/physiolres/archive.htm $y domovská stránka časopisu - plný text volně přístupný = fulltext
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 3 $z 0
- 990 __
- $a 20131021 $b ABA008
- 991 __
- $a 20151006120544 $b ABA008
- 999 __
- $a ok $b bmc $g 998510 $s 832580
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2008 $b 57 $c Suppl 1 $d S39-S48 $i 0862-8408 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- BMC __
- $a 2008 $b 57 $c Suppl 1 $d S39-S48 $i 0862-8408 $m From clinical to molecular endocrinology $n $x MED00170142
- GRA __
- $a NR7800 $p MZ0
- GRA __
- $a NR7809 $p MZ0
- LZP __
- $b NLK138 $a Pubmed-20131021