PMID- 25267796 OWN - NLM STAT- MEDLINE DCOM- 20150616 LR - 20211021 IS - 1935-5548 (Electronic) IS - 0149-5992 (Print) IS - 0149-5992 (Linking) VI - 37 IP - 12 DP - 2014 Dec TI - Effect of hypoglycemia on brain structure in people with type 2 diabetes: epidemiological analysis of the ACCORD-MIND MRI trial. PG - 3279-85 LID - 10.2337/dc14-0973 [doi] AB - OBJECTIVE: The effect of hypoglycemia related to treatment of type 2 diabetes mellitus (T2DM) on brain structure remains unclear. We aimed to assess whether symptomatic severe hypoglycemia is associated with brain atrophy and/or white matter abnormalities. RESEARCH DESIGN AND METHODS: We included T2DM participants with brain MRI from the Action to Control Cardiovascular Risk in Diabetes-Memory in Diabetes (ACCORD-MIND) trial. Symptomatic severe hypoglycemia was defined as blood glucose <2.8 mmol/L or symptoms resolved with treatments that required the assistance of another person or medical assistance (hypoglycemia requiring assistance [HA]). Standardized brain MRI was performed at baseline and at 40 months. Total brain volume (TBV) and abnormal white matter (AWM) volume were calculated using an automated computer algorithm. Brain MRI scans of hypoglycemic participants were also reviewed for local disease. RESULTS: Of the 503 T2DM participants (mean age, 62 years) with successful baseline and 40-month brain MRI, 28 had at least one HA episode during the 40-month follow-up. Compared with participants without HA, those with HA had marginally significant less atrophy (less decrease in TBV) from baseline to 40 months (-9.55 [95% CI -15.21, -3.90] vs. -15.38 [95% CI -16.64, -14.12], P = 0.051), and no significant increase of AWM volume (2.06 [95% CI 1.71, 2.49] vs. 1.84 [95% CI 1.76, 1.91], P = 0.247). In addition, no unexpected local signal changes or volume loss were seen on hypoglycemic participants' brain MRI scans. CONCLUSIONS: Our study suggests that hypoglycemia related to T2DM treatment may not accentuate brain pathology, specifically brain atrophy or white matter abnormalities. CI - (c) 2014 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. FAU - Zhang, Zi AU - Zhang Z AD - University of Pennsylvania, Philadelphia, PA. FAU - Lovato, James AU - Lovato J AD - Wake Forest University, Winston Salem, NC. FAU - Battapady, Harsha AU - Battapady H AD - University of Pennsylvania, Philadelphia, PA. FAU - Davatzikos, Christos AU - Davatzikos C AD - University of Pennsylvania, Philadelphia, PA. FAU - Gerstein, Hertzel C AU - Gerstein HC AD - McMaster University, Hamilton, Ontario, Canada. FAU - Ismail-Beigi, Faramarz AU - Ismail-Beigi F AD - Case Western Reserve University, Cleveland, OH. FAU - Launer, Lenore J AU - Launer LJ AD - National Institute on Aging, Bethesda, MD. FAU - Murray, Anne AU - Murray A AD - Hennepin County Medical Center, Minneapolis, MN. FAU - Punthakee, Zubin AU - Punthakee Z AD - McMaster University, Hamilton, Ontario, Canada. FAU - Tirado, Amilcar A AU - Tirado AA AD - Columbia University, New York, NY. FAU - Williamson, Jeff AU - Williamson J AD - Wake Forest University, Winston Salem, NC. FAU - Bryan, R Nick AU - Bryan RN AD - University of Pennsylvania, Philadelphia, PA nick.bryan@uphs.upenn.edu. FAU - Miller, Michael E AU - Miller ME AD - Wake Forest University, Winston Salem, NC. LA - eng SI - ClinicalTrials.gov/NCT00182910 GR - N01HC95184/HL/NHLBI NIH HHS/United States GR - N01-HC-95180/HC/NHLBI NIH HHS/United States GR - AG-0002/AG/NIA NIH HHS/United States GR - N01-HC-95184/HC/NHLBI NIH HHS/United States GR - N01HC95181/HL/NHLBI NIH HHS/United States GR - N01-HC-95182/HC/NHLBI NIH HHS/United States GR - R01 EB009234/EB/NIBIB NIH HHS/United States GR - N01-HC-95178/HC/NHLBI NIH HHS/United States GR - N01HC95182/HL/NHLBI NIH HHS/United States GR - N01-HC-95181/HC/NHLBI NIH HHS/United States GR - N01HC95178/HL/NHLBI NIH HHS/United States GR - N01HC95183/HL/NHLBI NIH HHS/United States GR - N01HC95179/HL/NHLBI NIH HHS/United States GR - N01-HC-95183/HC/NHLBI NIH HHS/United States GR - ImNIH/Intramural NIH HHS/United States GR - N01HC95180/HL/NHLBI NIH HHS/United States GR - N01-HC-95179/HC/NHLBI NIH HHS/United States PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, N.I.H., Extramural PT - Research Support, N.I.H., Intramural DEP - 20140929 PL - United States TA - Diabetes Care JT - Diabetes care JID - 7805975 RN - 0 (Blood Glucose) RN - 0 (Hypoglycemic Agents) SB - IM MH - Adult MH - Aged MH - Atrophy/chemically induced/epidemiology/pathology MH - Blood Glucose/drug effects MH - Brain/drug effects/*pathology/physiology MH - Cardiovascular Diseases/epidemiology/prevention & control MH - Diabetes Mellitus, Type 2/*drug therapy/epidemiology/pathology MH - Female MH - Humans MH - Hypoglycemia/*chemically induced/epidemiology/*pathology MH - Hypoglycemic Agents/*adverse effects MH - *Magnetic Resonance Imaging MH - Male MH - Memory/drug effects MH - Middle Aged MH - Risk Factors PMC - PMC4237972 EDAT- 2014/10/01 06:00 MHDA- 2015/06/17 06:00 PMCR- 2015/12/01 CRDT- 2014/10/01 06:00 PHST- 2014/10/01 06:00 [entrez] PHST- 2014/10/01 06:00 [pubmed] PHST- 2015/06/17 06:00 [medline] PHST- 2015/12/01 00:00 [pmc-release] AID - dc14-0973 [pii] AID - 0973 [pii] AID - 10.2337/dc14-0973 [doi] PST - ppublish SO - Diabetes Care. 2014 Dec;37(12):3279-85. doi: 10.2337/dc14-0973. Epub 2014 Sep 29.