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Genotypes of HLA, TCF7L2, and FTO as potential modifiers of the association between sweetened beverage consumption and risk of LADA and type 2 diabetes

Löfvenborg, Josefin E. ; Ahlqvist, Emma LU ; Alfredsson, Lars ; Andersson, Tomas ; Dorkhan, Mozhgan LU ; Groop, Leif LU ; Tuomi, Tiinamaija LU orcid ; Wolk, Alicja and Carlsson, Sofia LU (2020) In European Journal of Nutrition 59(1). p.127-135
Abstract

Purpose: Sweetened beverage consumption is associated with type 2 diabetes (T2D) and LADA. We investigated to what extent this association is mediated by BMI and whether it is modified by genotypes of HLA, TCF7L2 rs7903146, or FTO rs9939609. Methods: Swedish case–control data including incident cases of LADA (n = 386) and T2D (n = 1253) with matched population-based controls (n = 1545) was used. We estimated adjusted ORs of diabetes (95% CI) in relation to sweetened beverage intake (per daily 200 mL serving) and genotypes. The impact of BMI was estimated using causal mediation methodology. Associations with HOMA-IR and HOMA-B were explored through linear regression. Results: Sweetened beverage intake was associated with increased risk... (More)

Purpose: Sweetened beverage consumption is associated with type 2 diabetes (T2D) and LADA. We investigated to what extent this association is mediated by BMI and whether it is modified by genotypes of HLA, TCF7L2 rs7903146, or FTO rs9939609. Methods: Swedish case–control data including incident cases of LADA (n = 386) and T2D (n = 1253) with matched population-based controls (n = 1545) was used. We estimated adjusted ORs of diabetes (95% CI) in relation to sweetened beverage intake (per daily 200 mL serving) and genotypes. The impact of BMI was estimated using causal mediation methodology. Associations with HOMA-IR and HOMA-B were explored through linear regression. Results: Sweetened beverage intake was associated with increased risk of LADA (OR 1.15, 95% CI 1.03–1.29) and T2D (OR 1.21, 1.11–1.32). BMI was estimated to mediate 17% (LADA) and 56% (T2D) of the total risk. LADA was associated with risk variants of HLA (3.44, 2.63–4.50) and TCF7L2 (1.27, 1.00–1.61) but not FTO. Only among non-carriers of high-risk HLA genotypes was sweetened beverage intake associated with risk of LADA (OR 1.32, 1.06–1.56) and HOMA-IR (beta = 0.162, p = 0.0047). T2D was associated with TCF7L2 and FTO but not HLA, and the risk conferred by sweetened beverages appeared modified by FTO (OR 1.45, 95% CI 1.21–1.73 in non-carriers). Conclusions: Our findings suggest that sweetened beverages are associated with LADA and T2D partly through mediation by excess weight, but possibly also through other mechanisms including adverse effects on insulin sensitivity. These effects seem more pronounced in individuals without genetic susceptibility.

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author
; ; ; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Autoimmune diabetes, BMI, Genotype, Latent autoimmune diabetes in adults, Sweetened beverage, T2D, ANDIS, diabetes
in
European Journal of Nutrition
volume
59
issue
1
pages
9 pages
publisher
Springer
external identifiers
  • pmid:30656477
  • scopus:85060197106
ISSN
1436-6207
DOI
10.1007/s00394-019-01893-x
language
English
LU publication?
yes
id
70cdd0c8-f93a-4046-92ab-5f6e9abaee56
date added to LUP
2019-01-30 11:58:47
date last changed
2024-03-02 17:56:49
@article{70cdd0c8-f93a-4046-92ab-5f6e9abaee56,
  abstract     = {{<p>Purpose: Sweetened beverage consumption is associated with type 2 diabetes (T2D) and LADA. We investigated to what extent this association is mediated by BMI and whether it is modified by genotypes of HLA, TCF7L2 rs7903146, or FTO rs9939609. Methods: Swedish case–control data including incident cases of LADA (n = 386) and T2D (n = 1253) with matched population-based controls (n = 1545) was used. We estimated adjusted ORs of diabetes (95% CI) in relation to sweetened beverage intake (per daily 200 mL serving) and genotypes. The impact of BMI was estimated using causal mediation methodology. Associations with HOMA-IR and HOMA-B were explored through linear regression. Results: Sweetened beverage intake was associated with increased risk of LADA (OR 1.15, 95% CI 1.03–1.29) and T2D (OR 1.21, 1.11–1.32). BMI was estimated to mediate 17% (LADA) and 56% (T2D) of the total risk. LADA was associated with risk variants of HLA (3.44, 2.63–4.50) and TCF7L2 (1.27, 1.00–1.61) but not FTO. Only among non-carriers of high-risk HLA genotypes was sweetened beverage intake associated with risk of LADA (OR 1.32, 1.06–1.56) and HOMA-IR (beta = 0.162, p = 0.0047). T2D was associated with TCF7L2 and FTO but not HLA, and the risk conferred by sweetened beverages appeared modified by FTO (OR 1.45, 95% CI 1.21–1.73 in non-carriers). Conclusions: Our findings suggest that sweetened beverages are associated with LADA and T2D partly through mediation by excess weight, but possibly also through other mechanisms including adverse effects on insulin sensitivity. These effects seem more pronounced in individuals without genetic susceptibility.</p>}},
  author       = {{Löfvenborg, Josefin E. and Ahlqvist, Emma and Alfredsson, Lars and Andersson, Tomas and Dorkhan, Mozhgan and Groop, Leif and Tuomi, Tiinamaija and Wolk, Alicja and Carlsson, Sofia}},
  issn         = {{1436-6207}},
  keywords     = {{Autoimmune diabetes; BMI; Genotype; Latent autoimmune diabetes in adults; Sweetened beverage; T2D; ANDIS; diabetes}},
  language     = {{eng}},
  number       = {{1}},
  pages        = {{127--135}},
  publisher    = {{Springer}},
  series       = {{European Journal of Nutrition}},
  title        = {{Genotypes of HLA, TCF7L2, and FTO as potential modifiers of the association between sweetened beverage consumption and risk of LADA and type 2 diabetes}},
  url          = {{http://dx.doi.org/10.1007/s00394-019-01893-x}},
  doi          = {{10.1007/s00394-019-01893-x}},
  volume       = {{59}},
  year         = {{2020}},
}