Associations of maternal caffeine intake during pregnancy with abdominal and liver fat deposition in childhood.


Journal

Pediatric obesity
ISSN: 2047-6310
Titre abrégé: Pediatr Obes
Pays: England
ID NLM: 101572033

Informations de publication

Date de publication:
05 2020
Historique:
received: 13 10 2019
revised: 29 11 2019
accepted: 09 12 2019
pubmed: 29 12 2019
medline: 7 10 2020
entrez: 29 12 2019
Statut: ppublish

Résumé

Maternal caffeine intake during pregnancy is associated with an increased risk of childhood obesity. Studies in adults suggest that caffeine intake might also directly affect visceral and liver fat deposition, which are strong risk factors for cardio-metabolic disease. To assess the associations of maternal caffeine intake during pregnancy with childhood general, abdominal, and liver fat mass at 10 years of age. In a population-based cohort from early pregnancy onwards among 4770 mothers and children, we assessed maternal caffeine intake during pregnancy and childhood fat mass at age 10 years. Compared with children whose mothers consumed <2 units of caffeine per day during pregnancy, those whose mothers consumed 4-5.9 and ≥6 units of caffeine per day had a higher body mass index, total body fat mass index, android/gynoid fat mass ratio, and abdominal subcutaneous and visceral fat mass indices. Children whose mothers consumed 4-5.9 units of caffeine per day had a higher liver fat fraction. The associations with abdominal visceral fat and liver fat persisted after taking childhood total body fat mass into account. High maternal caffeine intake during pregnancy was associated with higher childhood body mass index, total body fat, abdominal visceral fat, and liver fat. The associations with childhood abdominal visceral fat and liver fat fraction were independent of childhood total body fat. This suggests differential fat accumulation in these depots, which may increase susceptibility to cardio-metabolic disease in later life.

Sections du résumé

BACKGROUND
Maternal caffeine intake during pregnancy is associated with an increased risk of childhood obesity. Studies in adults suggest that caffeine intake might also directly affect visceral and liver fat deposition, which are strong risk factors for cardio-metabolic disease.
OBJECTIVE
To assess the associations of maternal caffeine intake during pregnancy with childhood general, abdominal, and liver fat mass at 10 years of age.
METHODS
In a population-based cohort from early pregnancy onwards among 4770 mothers and children, we assessed maternal caffeine intake during pregnancy and childhood fat mass at age 10 years.
RESULTS
Compared with children whose mothers consumed <2 units of caffeine per day during pregnancy, those whose mothers consumed 4-5.9 and ≥6 units of caffeine per day had a higher body mass index, total body fat mass index, android/gynoid fat mass ratio, and abdominal subcutaneous and visceral fat mass indices. Children whose mothers consumed 4-5.9 units of caffeine per day had a higher liver fat fraction. The associations with abdominal visceral fat and liver fat persisted after taking childhood total body fat mass into account.
CONCLUSIONS
High maternal caffeine intake during pregnancy was associated with higher childhood body mass index, total body fat, abdominal visceral fat, and liver fat. The associations with childhood abdominal visceral fat and liver fat fraction were independent of childhood total body fat. This suggests differential fat accumulation in these depots, which may increase susceptibility to cardio-metabolic disease in later life.

Identifiants

pubmed: 31883239
doi: 10.1111/ijpo.12607
pmc: PMC7187321
doi:

Substances chimiques

Caffeine 3G6A5W338E

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e12607

Subventions

Organisme : ZonMw
ID : ZONMW_543003109
Pays : Netherlands
Organisme : European Research Council
ID : ERC-2014-CoG-648916
Pays : International

Informations de copyright

© 2019 The Authors. Pediatric Obesity published by John Wiley & Sons Ltd on behalf of World Obesity Federation.

Références

Obesity (Silver Spring). 2016 May;24(5):1170-7
pubmed: 27015969
J Dev Orig Health Dis. 2015 Dec;6(6):485-92
pubmed: 26434993
Pediatr Radiol. 2009 Jul;39(7):647-56
pubmed: 19415261
Am J Epidemiol. 2002 Mar 1;155(5):429-36
pubmed: 11867354
J Clin Epidemiol. 2005 Dec;58(12):1320-4
pubmed: 16291478
PLoS Med. 2019 Feb 11;16(2):e1002744
pubmed: 30742624
BMJ. 2017 Nov 22;359:j5024
pubmed: 29167102
Environ Health Perspect. 2014 Jul;122(7):761-7
pubmed: 24695368
BMC Med. 2014 Sep 19;12:174
pubmed: 25238871
Circulation. 2007 Jul 3;116(1):39-48
pubmed: 17576866
Int J Obes (Lond). 2018 Apr;42(4):608-617
pubmed: 29026216
Int J Obes (Lond). 2017 Sep;41(9):1440-1446
pubmed: 28487553
Cochrane Database Syst Rev. 2015 Jun 09;(6):CD006965
pubmed: 26058966
Toxicol Appl Pharmacol. 2012 Nov 1;264(3):395-403
pubmed: 22959462
Matern Child Health J. 2017 Jun;21(6):1297-1307
pubmed: 28110387
Biochim Biophys Acta. 2014 Mar;1842(3):473-81
pubmed: 23735216
Diabetes Res Clin Pract. 2007 Jun;76(3):383-9
pubmed: 17070955
Int J Obes (Lond). 2015 Apr;39(4):658-64
pubmed: 25388405
Adipocyte. 2013 Jul 1;2(3):128-34
pubmed: 23991358
Am J Clin Nutr. 2010 Jun;91(6):1691-8
pubmed: 20427730
Toxicology. 2019 Apr 1;417:23-34
pubmed: 30776459
Biol Sex Differ. 2012 May 31;3(1):13
pubmed: 22651247
Aliment Pharmacol Ther. 2012 Jan;35(1):76-82
pubmed: 22059453
Biochem Pharmacol. 1962 Feb;11:166-8
pubmed: 13899873
PLoS One. 2012;7(9):e44497
pubmed: 22970234
BMJ. 2008 Nov 03;337:a2332
pubmed: 18981029
BMJ Open. 2018 Apr 23;8(3):e018895
pubmed: 29685923
BMJ. 2000 May 6;320(7244):1240-3
pubmed: 10797032
J Magn Reson Imaging. 2011 Oct;34(4):729-749
pubmed: 22025886
Birth Defects Res B Dev Reprod Toxicol. 2011 Apr;92(2):152-87
pubmed: 21370398
Am J Clin Nutr. 2019 Jun 1;109(6):1648-1655
pubmed: 31136661
Pediatr Res. 2000 Mar;47(3):316-23
pubmed: 10709729
Public Health Nutr. 2016 May;19(7):1233-44
pubmed: 26329421
J Clin Pharmacol. 2016 May;56(5):590-6
pubmed: 26358647
Eur J Gastroenterol Hepatol. 2017 Feb;29(2):e8-e12
pubmed: 27824642
Pediatr Obes. 2020 May;15(5):e12607
pubmed: 31883239
Eur J Epidemiol. 2016 Dec;31(12):1243-1264
pubmed: 28070760
Nutrition. 2013 Jul-Aug;29(7-8):982-7
pubmed: 23602227
BMC Med. 2013 Feb 19;11:42
pubmed: 23421532
Toxicol Lett. 2014 Jan 30;224(3):311-8
pubmed: 24239806
Obesity (Silver Spring). 2016 Jun;24(6):1320-7
pubmed: 27094573
Int J Obes Relat Metab Disord. 2002 Jul;26(7):947-52
pubmed: 12080448
Circulation. 2011 Dec 13;124(24):e837-41
pubmed: 22156000
Obes Rev. 2011 May;12(5):e504-15
pubmed: 21348916
Clin Nutr. 2016 Dec;35(6):1269-1281
pubmed: 27060021
Clin Pharmacol Ther. 1979 Apr;25(4):447-53
pubmed: 428190
Am J Clin Nutr. 1990 Dec;52(6):953-9
pubmed: 2239792

Auteurs

Ellis Voerman (E)

The Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Department of Pediatrics, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Vincent Wv Jaddoe (VW)

The Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Department of Pediatrics, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Mirjam E Hulst (ME)

The Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Department of Pediatrics, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Edwin Hg Oei (EH)

Department of Radiology & Nuclear Medicine, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Romy Gaillard (R)

The Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Department of Pediatrics, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH