Diabet. Med. 29, e436e439 (2012) Abstract Aims Gestational diabetes mellitus affects approximately 7% of all pregnant women. Some of these women develop autoantibodies that are generally characteristic of Type 1 diabetes. Autoantibodies targeting glutamic acid decarboxylase and tyrosine phosphatase-like protein are the most frequently reported. A recently identified autoantigen in Type 1 diabetes is zinc transporter 8. Some reports suggest that the frequency of zinc transporter 8 antibodies is as high as glutamic acid decarboxylase antibodies in Type 1 diabetes and thus a good diagnostic marker for autoimmune diabetes. There are currently no reports of zinc transporter 8 antibodies in gestational diabetes. The aim of this pilot study was to investigate the frequency of zinc transporter 8 antibodies in patients at clinical onset of gestational diabetes mellitus. Methods Subjects included in this pilot study were all diagnosed with gestational diabetes at Skane University Hospital, Lund, Sweden, 20092010 (n = 193). Sera samples were analysed for antibodies using a commercial enzyme-linked immunosorbent assay according to the manufacturers instructions. Results We found that 19/193 patients with gestational diabetes, diagnosed in 20092010, were positive for at least one autoantibody. Glutamic acid decarboxylase was the most common single autoantibody (52.6%; 10/19), followed by zinc transporter 8 (21.1%; 4/19) and tyrosine phosphatase-like protein (15.8%; 3/19). Combinations of two or more antibodies were rare (10.5%; 2/19). Conclusions In this study, we found that zinc transporter 8 added 2.1% (4/193) of autoantibody positivity in women with gestational diabetes who were negative for glutamic acid decarboxylase and tyrosine phosphatase-like protein antibodies. Glutamic acid decarboxylase was still the most prevalent autoantibody in gestational diabetes, but, as zinc transporter 8 was present even in the absence of glutamic acid decarboxylase, this autoantibody could be an important independent marker of autoimmunity in gestational diabetes.
机构:
Univ Airlangga, Doctoral Program Publ Hlth, Surabaya, Indonesia
Univ Airlangga, Fac Publ Hlth, Kampus C Unair, Sukolilo Surabaya, Jawa Timur, IndonesiaUniv Airlangga, Doctoral Program Publ Hlth, Surabaya, Indonesia
Dewi, Ratna Sari
Isfandiari, Muhammad Atoillah
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Univ Airlangga, Dept Publ Hlth, Surabaya, IndonesiaUniv Airlangga, Doctoral Program Publ Hlth, Surabaya, Indonesia
Isfandiari, Muhammad Atoillah
Martini, Santi
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Univ Airlangga, Dept Publ Hlth, Surabaya, IndonesiaUniv Airlangga, Doctoral Program Publ Hlth, Surabaya, Indonesia
Martini, Santi
Yi-Li, Chung
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机构:
Natl Cheng Kung Univ, Coll Med, Dept Publ Hlth, Tainan, TaiwanUniv Airlangga, Doctoral Program Publ Hlth, Surabaya, Indonesia
机构:
South African Med Res Council, BRIP, Cape Town, South Africa
Univ Pretoria, Fac Hlth Sci, Dept Obstet & Gynaecol, Pretoria, South AfricaSouth African Med Res Council, BRIP, Cape Town, South Africa
Dias, S.
Adam, S.
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Univ Pretoria, Fac Hlth Sci, Dept Obstet & Gynaecol, Pretoria, South AfricaSouth African Med Res Council, BRIP, Cape Town, South Africa
Adam, S.
Rheeder, P.
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Univ Pretoria, Fac Hlth Sci, Dept Internal Med, Pretoria, South AfricaSouth African Med Res Council, BRIP, Cape Town, South Africa
Rheeder, P.
Pheiffer, C.
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South African Med Res Council, BRIP, Cape Town, South Africa
Stellenbosch Univ, Fac Med & Hlth Sci, Dept Biomed Sci, Div Med Physiol, Cape Town, South AfricaSouth African Med Res Council, BRIP, Cape Town, South Africa
Pheiffer, C.
SAMJ SOUTH AFRICAN MEDICAL JOURNAL,
2019,
109
(07):
: 463
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