PMID- 24427296 OWN - NLM STAT- MEDLINE DCOM- 20141017 LR - 20211021 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 9 IP - 1 DP - 2014 TI - Expression of obesity markers and Persistent Organic Pollutants levels in adipose tissue of obese patients: reinforcing the obesogen hypothesis? PG - e84816 LID - 10.1371/journal.pone.0084816 [doi] LID - e84816 AB - INTRODUCTION: Persistent Organic Pollutants (POPs) accumulate in adipose tissue and some are described to possess endocrine disrupting capacities. Therefore, it is important to evaluate their effects on key endocrine pathways in adipose tissue (AT), to further evaluate their potential role in metabolic pathologies such as obesity. OBJECTIVES: THE AIM IS TWOFOLD: (i) evaluate gene expression levels of obesity marker genes, i.e. the adipokines leptin (LEP), adiponectin (ADIPOQ) and Tumor Necrosis Factor alpha (TNFalpha) and the nuclear receptor, Peroxisome Proliferator Activated Receptor gamma (PPARgamma) in paired subcutaneous (SAT) and visceral (VAT) AT of obese subjects (n = 50) and to relate these values to serum concentrations of LEP and ADIPOQ (ii) evaluate the association of expression levels of marker genes in AT and serum with POP concentrations in AT. RESULTS AND CONCLUSIONS: Leptin and adiponectin levels in serum were positively correlated to respectively expression levels of leptin in SAT and adiponectin in VAT. Our study shows more significant correlations between gene expression of obesity marker genes and POP concentrations in VAT compared to SAT. Since VAT is more important than SAT in pathologies associated with obesity, this suggests that POPs are able to influence the association between obesity and the development of associated pathologies. Moreover, this finding reveals the importance of VAT when investigating the obesogen hypothesis. Concerning PPARgamma expression in VAT, negative correlations with polychlorinated biphenyls (PCBs) concentrations were found in non T2D patients. LEP serum concentrations correlated with several PCBs in women whereas in men no correlations were found. This strengthens the potential importance of gender differences in obesity and within the obesogen hypothesis. FAU - Pereira-Fernandes, Anna AU - Pereira-Fernandes A AD - Systemic Physiological and Ecotoxicological Research (SPHERE), Department of Biology, University of Antwerp, Antwerp, Belgium. FAU - Dirinck, Eveline AU - Dirinck E AD - Department of Endocrinology, Diabetology and Metabolism, Antwerp University Hospital, University of Antwerp, Edegem, Belgium. FAU - Dirtu, Alin C AU - Dirtu AC AD - Toxicological Centre, University of Antwerp, Antwerp, Belgium. FAU - Malarvannan, Govindan AU - Malarvannan G AD - Toxicological Centre, University of Antwerp, Antwerp, Belgium. FAU - Covaci, Adrian AU - Covaci A AD - Toxicological Centre, University of Antwerp, Antwerp, Belgium. FAU - Van Gaal, Luc AU - Van Gaal L AD - Department of Endocrinology, Diabetology and Metabolism, Antwerp University Hospital, University of Antwerp, Edegem, Belgium. FAU - Vanparys, Caroline AU - Vanparys C AD - Systemic Physiological and Ecotoxicological Research (SPHERE), Department of Biology, University of Antwerp, Antwerp, Belgium. FAU - Jorens, Philippe G AU - Jorens PG AD - Department of Clinical Pharmacology, Antwerp University Hospital, University of Antwerp, Edegem, Belgium. FAU - Blust, Ronny AU - Blust R AD - Systemic Physiological and Ecotoxicological Research (SPHERE), Department of Biology, University of Antwerp, Antwerp, Belgium. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20140110 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Biomarkers) SB - IM MH - Adipose Tissue/*metabolism MH - Adolescent MH - Adult MH - Biomarkers/blood/metabolism MH - Female MH - *Gene Expression MH - Humans MH - Intra-Abdominal Fat/metabolism MH - Male MH - Middle Aged MH - Obesity/*genetics/*metabolism MH - Subcutaneous Fat/metabolism MH - Young Adult PMC - PMC3888404 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2014/01/16 06:00 MHDA- 2014/10/18 06:00 PMCR- 2014/01/10 CRDT- 2014/01/16 06:00 PHST- 2013/07/26 00:00 [received] PHST- 2013/11/27 00:00 [accepted] PHST- 2014/01/16 06:00 [entrez] PHST- 2014/01/16 06:00 [pubmed] PHST- 2014/10/18 06:00 [medline] PHST- 2014/01/10 00:00 [pmc-release] AID - PONE-D-13-30532 [pii] AID - 10.1371/journal.pone.0084816 [doi] PST - epublish SO - PLoS One. 2014 Jan 10;9(1):e84816. doi: 10.1371/journal.pone.0084816. eCollection 2014.