CXC chemokine ligand 16 is increased in gestational diabetes mellitus and preeclampsia and associated with lipoproteins in gestational diabetes mellitus at 5years follow-up

被引:21
作者
Lekva, Tove [1 ]
Michelsen, Annika E. [1 ,2 ]
Aukrust, Pal [1 ,2 ,3 ,4 ,5 ]
Roland, Marie Cecilie Paasche [6 ,7 ]
Henriksen, Tore [2 ,6 ]
Bollerslev, Jens [2 ,8 ]
Ueland, Thor [1 ,2 ,5 ]
机构
[1] Natl Hosp Norway, Oslo Univ Hosp, Internal Med Res Inst, Sognsvannsveien 20, N-0027 Oslo, Norway
[2] Univ Oslo, Fac Med, Oslo, Norway
[3] Natl Hosp Norway, Oslo Univ Hosp, Sect Clin Immunol & Infect Dis, Oslo, Norway
[4] Univ Oslo, KG Jebsen Inflammat Res Ctr, Oslo, Norway
[5] Univ Tromso, KG Jebsen Thrombosis Res & Expertise Ctr, Tromso, Norway
[6] Natl Hosp Norway, Oslo Univ Hosp, Dept Obstet, Oslo, Norway
[7] Natl Hosp Norway, Oslo Univ Hosp, Norwegian Natl Advisory Unit Womens Hlth, Oslo, Norway
[8] Natl Hosp Norway, Oslo Univ Hosp, Sect Specialized Endocrinol, Dept Endocrinol, Oslo, Norway
关键词
CXC chemokine ligand 16; gestational diabetes mellitus; preeclampsia; ACUTE CORONARY SYNDROMES; LOW-DENSITY-LIPOPROTEIN; SCAVENGER RECEPTOR; SOLUBLE CXCL16; CARDIOVASCULAR-DISEASE; METABOLIC SYNDROME; SERUM CXCL16; RISK; ATHEROSCLEROSIS; INFLAMMATION;
D O I
10.1177/1479164117728011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Women with a history of gestational diabetes mellitus and preeclampsia are at increased risk of cardiovascular disease later in life, but the mechanism remains unclear. The aim of the study was to evaluate the association between CXC chemokine ligand 16 and indices of glucose metabolism, dyslipidemia and systemic inflammation in gestational diabetes mellitus and preeclampsia. Methods: This sub-study of the population-based prospective cohort included 310 women. Oral glucose tolerance test was performed during pregnancy and 5years later along with lipid analysis. CXC chemokine ligand 16 was measured in plasma (protein) and peripheral blood mononuclear cells (messenger RNA) during pregnancy and at follow-up. Results: Circulating CXC chemokine ligand 16 was higher in gestational diabetes mellitus women early in pregnancy and at follow-up, while higher in preeclampsia women late in pregnancy compared to control women. Messenger RNA of CXC chemokine ligand 16 in peripheral blood mononuclear cells were lower in gestational diabetes mellitus and preeclampsia women compared to control women. Increased circulating CXC chemokine ligand 16 level was associated with a higher apolipoprotein B and low-density lipoprotein cholesterol in gestational diabetes mellitus women but not in normal pregnancy at follow-up. Conclusion: Our study shows that women with gestational diabetes mellitus and preeclampsia had a dysregulated CXC chemokine ligand 16 during pregnancy, and in gestational diabetes mellitus, the increase in CXC chemokine ligand 16 early in pregnancy and after 5years was strongly associated with their lipid profile.
引用
收藏
页码:525 / 533
页数:9
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