Perinatal famine is associated with excess risk of proliferative retinopathy in patients with type 2 diabetesUmeå University, Faculty of Medicine, Department of Odontology. Broad Institute of Harvard and MIT, MA, Cambridge, United States.
Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona and CIBERDEM, Barcelona, Spain.
Department of Clinical Science, Center for Diabetes Research, University of Bergen, Bergen, Norway.
Chernihiv Regional Hospital, Chernihiv, Ukraine.
City Hospital No 2, Chernihiv, Ukraine.
City Hospital No 1, Chernihiv, Ukraine.
Department of Health Care of Chernihiv Regional State Administration, Chernihiv, Ukraine.
Komisarenko Institute of Endocrinology and Metabolism, Kyiv, Ukraine.
Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona and CIBERDEM, Barcelona, Spain.
Department of Clinical Sciences, Lund University Diabetes Center, Skåne University Hospital, Malmoe, Sweden.
Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona and CIBERDEM, Barcelona, Spain.
Department of Clinical Sciences, Lund University Diabetes Center, Skåne University Hospital, Malmoe, Sweden.
Department of Clinical Sciences, Lund University Diabetes Center, Skåne University Hospital, Malmoe, Sweden.
Komisarenko Institute of Endocrinology and Metabolism, Kyiv, Ukraine; Shupyk National Medical Academy of Postgraduate Education, Kyiv, Ukraine.
Laboratory of Epigenetics, Chebotarev Institute of Gerontology, Kyiv, Ukraine.
Hong Kong Institute of Diabetes and Obesity, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Steno Diabetes Center Copenhagen, Copenhagen, Denmark.
Department of Clinical Science, Center for Diabetes Research, University of Bergen, Bergen, Norway; Department of Clinical Sciences, Lund University Diabetes Center, Skåne University Hospital, Malmoe, Sweden.
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2022 (English)In: Acta Ophthalmologica, ISSN 1755-375X, E-ISSN 1755-3768, Vol. 100, no 2, p. e539-e545Article in journal (Refereed) Published
Abstract [en]
Purpose: Intrauterine undernutrition is associated with increased risk of type 2 diabetes. Children born premature or small for gestational age were reported to have abnormal retinal vascularization. However, whether intrauterine famine act as a trigger for diabetes complications, including retinopathy, is unknown. The aim of the current study was to evaluate long-term effects of perinatal famine on the risk of proliferative diabetic retinopathy (PDR).
Methods: We studied the risk for PDR among type 2 diabetes patients exposed to perinatal famine in two independent cohorts: the Ukrainian National Diabetes Registry (UNDR) and the Hong Kong Diabetes Registry (HKDR). We analysed individuals born during the Great Famine (the Holodomor, 1932–1933) and the WWII (1941–1945) famine in 101 095 (3601 had PDR) UNDR participants. Among 3021 (251 had PDR) HKDR participants, we studied type 2 diabetes patients exposed to perinatal famine during the WWII Japanese invasion in 1942–1945.
Results: During the Holodomor and WWII, perinatal famine was associated with a 1.76-fold (p = 0.019) and 3.02-fold (p = 0.001) increased risk of severe PDR in the UNDR. The risk for PDR was 1.66-fold elevated among individuals born in 1942 in the HKDR (p < 0.05). The associations between perinatal famine and PDR remained statistically significant after corrections for HbA1c in available 18 507 UNDR (padditive interaction < 0.001) and in 3021 HKDR type 2 diabetes patients (p < 0.05).
Conclusion: In conclusion, type 2 diabetes patients, exposed to perinatal famine, have increased risk of PDR compared to those without perinatal famine exposure. Further studies are needed to understand the underlying mechanisms and to extend this finding to other diabetes complications.
Place, publisher, year, edition, pages
John Wiley & Sons, 2022. Vol. 100, no 2, p. e539-e545
Keywords [en]
diabetic retinopathy, famine, intrauterine exposure, microvasculature, type 2 diabetes, undernutrition
National Category
Endocrinology and Diabetes
Identifiers
URN: urn:nbn:se:umu:diva-185545DOI: 10.1111/aos.14948ISI: 000665634700001PubMedID: 34169655Scopus ID: 2-s2.0-85108415228OAI: oai:DiVA.org:umu-185545DiVA, id: diva2:1575776
2021-06-302021-06-302022-08-05Bibliographically approved