Bigger babies more likely to develop diabetes

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Credit: Kelly Sikkema/Unsplash
Credit: Kelly Sikkema/Unsplash

A study of over 180,000 people has found that babies born 2.5 kg or heavier are more likely to be at risk of developing type 2 diabetes as adults. The team of US researchers looked at data from the UK Biobank, which is tracking links between genetic and lifestyle factors and various diseases common in middle and old age. Their findings suggest that the link between birthweight and risk of developing type 2 diabetes may be influenced by a hormone called IGF-1, which is similar to insulin and affects childhood growth. However, this is an observational study, so can't establish a cause.

News release

From: The BMJ

Birthweight strongly linked to type 2 diabetes risk in adulthood

Weight of 2.5 kg+ associated with lower levels of key glucose regulator hormone 

A birthweight of 2.5 kg or more is strongly linked to the risk of developing type 2 diabetes in adulthood, finds research published in the online journal BMJ Open Diabetes Research & Care.

It is associated with lower circulating levels of insulin-like growth factor-1, or IGF-1 for short, a hormone similar to insulin that affects childhood growth and energy metabolism in adults.

Compelling evidence indicates that susceptibility to type 2 diabetes over the life course is determined jointly by risk factors in both early life and adulthood, say the researchers.

To find out if there might be any association between adult circulating IGF-1 levels, birthweight, and the risk of developing type 2 diabetes, the researchers drew on data from 112,736 women and 68,354 men taking part in the UK Biobank study.

The UK Biobank is a large population-based study, which recruited its 37–73 year old participants between 2006 and 2010. It is tracking the potential impact of genetic and lifestyle factors on a wide range of common diseases of middle-and old age.

At recruitment, participants provided social and demographic details, as well as information on their usual diet, lifestyle (smoking status, alcohol intake, sleep duration and habitual physical activity), early life factors (birthweight and maternal smoking) and medical history.

They also provided blood, urine, and saliva samples and their height, weight, body mass index (BMI), body circumferences (waist, hip, and limbs), and skinfold thickness were measured.

Blood was checked for IGF-1, cholesterol, triglycerides and an indicator of inflammation, C-reactive protein. And repeat measures of IGF-1 were available from 17,699 participants. Information on the development of type 2 diabetes was obtained from self-report, hospital records, and death certificates.

During an average monitoring period of nearly 10 years, 3299 people developed type 2 diabetes.

Participants with lower levels of IGF-1 tended to be older and more likely to live in a deprived area. They were also more likely to have lifestyle and clinical risk factors for diabetes.

Nevertheless, a clear inverse association emerged between IGF-1 levels and type 2 diabetes: the lower the IGF-1 level, the higher was the risk of type 2 diabetes.

But birthweight significantly altered this association, although only for those whose weight was 2.5 kg or more at birth, and only in men.

Compared with those in the lowest 20% of IGF-1 levels, the odds of type 2 diabetes were 14% lower for those in the second lowest 20%, and up to 36% lower for those in the highest 20% of IGF-1 levels.

The findings held true, irrespective of any genetic predisposition to birthweight.

This is an observational study, and as such, can’t establish cause. Nor was there any information on whether the births had been premature or full term, or on ethnicity--factors that may well be influential, say the researchers.

Nevertheless, their findings echo those of other epidemiological studies, they note. “Our findings highlight the importance of early-life risk factors in the development of the lifecourse prevention strategies targeting IGF-1 and [type 2 diabetes],” they conclude.

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Research The BMJ, Web page The URL will go live after the embargo ends.
Journal/
conference:
BMJ Open Diabetes Research & Care
Research:Paper
Organisation/s: Tulane University, USA
Funder: The study was supported by grants from the National Heart, Lung, and Blood Institute (HL071981, HL034594, and HL126024) and the National Institute of Diabetes and Digestive and Kidney Diseases (DK115679, DK091718, DK100383, and DK078616).
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