Tryptophan and purine metabolites are consistently upregulated in the urinary metabolome of patients diagnosed with gestational diabetes mellitus throughout pregnancy: A longitudinal metabolomics study of Chinese pregnant women part 2
被引:76
作者:
Law, Kai P.
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Chongqing Med Univ, China Canada New Zealand Joint Lab Maternal & Foe, Mass Spectrometry Ctr, Chongqing, Peoples R ChinaChongqing Med Univ, China Canada New Zealand Joint Lab Maternal & Foe, Mass Spectrometry Ctr, Chongqing, Peoples R China
Law, Kai P.
[1
]
Han, Ting-Li
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Chongqing Med Univ, China Canada New Zealand Joint Lab Maternal & Foe, Mass Spectrometry Ctr, Chongqing, Peoples R ChinaChongqing Med Univ, China Canada New Zealand Joint Lab Maternal & Foe, Mass Spectrometry Ctr, Chongqing, Peoples R China
Han, Ting-Li
[1
]
Mao, Xun
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Chongqing Med Univ, China Canada New Zealand Joint Lab Maternal & Foe, Mass Spectrometry Ctr, Chongqing, Peoples R China
Chongqing Med Univ, Affiliated Hosp 1, Dept Obstet & Gynaecol, Chongqing, Peoples R ChinaChongqing Med Univ, China Canada New Zealand Joint Lab Maternal & Foe, Mass Spectrometry Ctr, Chongqing, Peoples R China
Mao, Xun
[1
,2
]
Zhang, Hua
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Chongqing Med Univ, China Canada New Zealand Joint Lab Maternal & Foe, Mass Spectrometry Ctr, Chongqing, Peoples R China
Chongqing Med Univ, Affiliated Hosp 1, Dept Obstet & Gynaecol, Chongqing, Peoples R ChinaChongqing Med Univ, China Canada New Zealand Joint Lab Maternal & Foe, Mass Spectrometry Ctr, Chongqing, Peoples R China
Zhang, Hua
[1
,2
]
机构:
[1] Chongqing Med Univ, China Canada New Zealand Joint Lab Maternal & Foe, Mass Spectrometry Ctr, Chongqing, Peoples R China
[2] Chongqing Med Univ, Affiliated Hosp 1, Dept Obstet & Gynaecol, Chongqing, Peoples R China
Background: Gestational diabetes mellitus (GDM) is a pathological state of glucose intolerance associated with adverse pregnancy outcomes and an increased risk of developing maternal type 2 diabetes later in life. The mechanisms underlying GDM development are not fully understood. We examined the pathophysiology of GDM through comprehensive metabolic profiling of maternal urine, using participants from a longitudinal cohort of normal pregnancies and pregnancies complicated by GDM. Methods: Based on ultra-performance liquid chromatography/hybrid quadrupole time-of-flight mass spectrometry, an untargeted metabolomics study was performed to explore the differences in the urinary metabolome of GDM cases and healthy controls over the course of pregnancy. Multilevel statistical approaches were employed to address the complex metabolomic data obtained from a longitudinal cohort. Results: The results indicated that tryptophan and purine metabolism was associated with GDM. The tryptophan-kynurenine pathway was activated in the GDM subjects before placental hormones or the fetoplacental unit could have produced any physiological effect. Hypoxanthine, xanthine, xanthosine, and 1-methylhypoxanthine were all elevated in the urine metabolome of subjects with GDM. Catabolism of purine nucleosides leads ultimately to the production of uric acid, which discriminated the subjects with GDM from controls. Conclusions: The results support the notion that GDM may be a predisposed condition, or prediabetic state, which is manifested during pregnancy. This challenges the conventional view of the pathogenesis of GDM, which assumes placental hormones are the major causes of insulin resistance in GDM. (C) 2017 Elsevier B.V. All rights reserved.
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Univ Tasmania, Sch Math & Phys, Hobart, Tas, AustraliaUniv Tasmania, Sch Math & Phys, Hobart, Tas, Australia
Karpievitch, Yuliya V.
;
Nikolic, Sonja B.
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Univ Tasmania, Menzies Res Inst Tasmania, Hobart, Tas, AustraliaUniv Tasmania, Sch Math & Phys, Hobart, Tas, Australia
Nikolic, Sonja B.
;
Wilson, Richard
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Univ Tasmania, Cent Sci Lab, Hobart, Tas, AustraliaUniv Tasmania, Sch Math & Phys, Hobart, Tas, Australia
Wilson, Richard
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Sharman, James E.
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Univ Tasmania, Cent Sci Lab, Hobart, Tas, AustraliaUniv Tasmania, Sch Math & Phys, Hobart, Tas, Australia
Sharman, James E.
;
Edwards, Lindsay M.
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Kings Coll London, Ctr Human & Aerosp Physiol Sci, London, England
GlaxoSmithKline R&D, Fibrosis Discovery Performance Unit, Stevenage, Herts, EnglandUniv Tasmania, Sch Math & Phys, Hobart, Tas, Australia
机构:
Univ Tasmania, Sch Math & Phys, Hobart, Tas, AustraliaUniv Tasmania, Sch Math & Phys, Hobart, Tas, Australia
Karpievitch, Yuliya V.
;
Nikolic, Sonja B.
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h-index: 0
机构:
Univ Tasmania, Menzies Res Inst Tasmania, Hobart, Tas, AustraliaUniv Tasmania, Sch Math & Phys, Hobart, Tas, Australia
Nikolic, Sonja B.
;
Wilson, Richard
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h-index: 0
机构:
Univ Tasmania, Cent Sci Lab, Hobart, Tas, AustraliaUniv Tasmania, Sch Math & Phys, Hobart, Tas, Australia
Wilson, Richard
;
Sharman, James E.
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h-index: 0
机构:
Univ Tasmania, Cent Sci Lab, Hobart, Tas, AustraliaUniv Tasmania, Sch Math & Phys, Hobart, Tas, Australia
Sharman, James E.
;
Edwards, Lindsay M.
论文数: 0引用数: 0
h-index: 0
机构:
Kings Coll London, Ctr Human & Aerosp Physiol Sci, London, England
GlaxoSmithKline R&D, Fibrosis Discovery Performance Unit, Stevenage, Herts, EnglandUniv Tasmania, Sch Math & Phys, Hobart, Tas, Australia