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Sanna Mustaniemi, Marja Vääräsmäki, Johan G Eriksson, Mika Gissler, Hannele Laivuori, Hilkka Ijäs, Aini Bloigu, Eero Kajantie and Laure Morin-Papunen

) primiparous women of normal weight (BMI <25 kg/m 2 ) who were under 25 years of age and had no family history of diabetes, and (2) multiparous women of normal weight (BMI <25 kg/m 2 ) who were under 40 years of age and had no history of GDM or macrosomic

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Ling-Jun Li, Izzuddin M Aris, Lin Lin Su, Yap Seng Chong, Tien Yin Wong, Kok Hian Tan and Jie Jin Wang

maternal education, household income, family history of diabetes, parity, pre-pregnancy weight, smoking and alcohol drinking in the past one year and physical activity in the past three months. Weight gain between baseline and follow-up visits (5-year

Open access

N Bergmann, F Gyntelberg and J Faber

demands Q FPG ≥7.0 or HbA1c ≥6.5 or physician diagnosed DM, or use of diabetic medication Age, gender, education, family history of diabetes, smoking history, sport intensity, and depressive symptoms Logistics regressions predicting the incidence of

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Helga Schultz, Svend Aage Engelholm, Eva Harder, Ulrik Pedersen-Bjergaard and Peter Lommer Kristensen

, median (IQR) 9 (8–20) 8 (7–12) 13 (8–28) 30 (18–33)  Number of plasma glucose measurements until time of diagnosis, median (IQR) 6 (3–8) 7 (4–15)  Family history of diabetes (%)* 35 (27) 18 (24) N  = 73 12 (30) N  = 39

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Meena Asmar, Ali Asmar, Lene Simonsen, Flemming Dela, Jens Juul Holst and Jens Bülow

summarized in Table 1 . The subjects also took part in a recent, reported study ( 14 ). None of the subjects had a positive family history of diabetes. All had normal fasting blood concentrations of glucose, lipids and hemoglobin and normal renal and hepatic

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Henrik H Thomsen, Holger J Møller, Christian Trolle, Kristian A Groth, Anne Skakkebæk, Anders Bojesen, Christian Høst and Claus H Gravholt

positive family history of diabetes. Men who were planning to participate in competitive sport events during the subsequent year were not included. All had levels of testosterone 18.6 (8.3–32.9) nmol/l as well as luteinizing hormone (LH) 4.8 (1.7–8.1) IU

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Kim K B Clemmensen, Jonas S Quist, Dorte Vistisen, Daniel R Witte, Anna Jonsson, Oluf Pedersen, Torben Hansen, Jens J Holst, Torsten Lauritzen, Marit E Jørgensen, Signe Torekov and Kristine Færch

included. It consisted only of middle-aged and older individuals, and only half of the invited individuals participated. The attendees were more likely to be men, overweight and to have a family history of diabetes ( 16 ). We cannot rule out that there are

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E R Polina, F M Oliveira, R C Sbruzzi, D Crispim, L H Canani and K G Santos

2001 ( n  = 67) or 2017 and 2018 ( n  = 72). A questionnaire was used to collect data regarding age, gender, skin colour/ethnicity, use of medication and diabetes-related information. Blood donors with a known personal and/or first-degree family history

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Anita Hokken-Koelega, Aart-Jan van der Lely, Berthold Hauffa, Gabriele Häusler, Gudmundur Johannsson, Mohamad Maghnie, Jesús Argente, Jean DeSchepper, Helena Gleeson, John W Gregory, Charlotte Höybye, Fahrettin Keleştimur, Anton Luger, Hermann L Müller, Sebastian Neggers, Vera Popovic-Brkic, Eleonora Porcu, Lars Sävendahl, Stephen Shalet, Bessie Spiliotis and Maithé Tauber

obese and to seek low-threshold clinical care in the presence of fatigue, weight gain, and a family history of diabetes, cardiovascular disease or hypertension. The goals of the second breakout workshop were to garner information on current clinical

Open access

Huguette S Brink, Aart Jan van der Lely and Joke van der Linden

identified ( 98 ). Furthermore, in a large prospective cohort ( n  = 7929), the best performing model, based on ethnicity, BMI, family history of diabetes and history of GD, showed a sensitivity, specificity and AUC of 73% (66–79), 81% (80–82) and 0.824 (0