Occurrence and Predictors of Persistent Impaired Glucose Tolerance After Acute Ischemic Stroke or Transient Ischemic Attack

被引:9
|
作者
Fonville, Susanne [1 ]
den Hertog, Heleen M. [1 ,2 ]
Zandbergen, Adrienne A. M. [3 ]
Koudstaal, Peter J. [1 ]
Lingsma, Hester F. [4 ]
机构
[1] Erasmus MC, Dept Neurol, POB 2040, NL-3000 CA Rotterdam, Netherlands
[2] Med Spectrum Twente, Dept Neurol, Enschede, Netherlands
[3] Ikazia Hosp, Dept Internal Med, Rotterdam, Netherlands
[4] Erasmus MC, Dept Publ Hlth, NL-3000 CA Rotterdam, Netherlands
来源
关键词
Stroke; TIA; impaired glucose tolerance; prediction model; NONDIABETIC PATIENTS; INSULIN-RESISTANCE; PREVALENCE; METABOLISM; RISK;
D O I
10.1016/j.jstrokecerebrovasdis.2014.01.012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Impaired glucose tolerance is often present in patients with a transient ischemic attack ( TIA) or ischemic stroke and doubles the risk of recurrent stroke. This impaired glucose tolerance can be transient, reflecting an acute stress response, or persistent, representing undiagnosed impaired glucose metabolism possibly requiring treatment. We aimed to assess the occurrence of persistent impaired glucose tolerance after a stroke or TIA and to develop a prediction model to identify patients at risk of persistent impaired glucose tolerance. Methods: Patients admitted to the stroke unit or TIA clinic of the Erasmus Medical Center with ischemic stroke or TIA and impaired glucose tolerance ( 2- hour postload glucose level of 7.811.0 mmol/ L) were consecutively enrolled between July 2009 and June 2012. The oral glucose tolerance test was repeated after 3 months and patients were classified as having transient impaired glucose tolerance or persistent impaired glucose tolerance. We developed a prediction model by means of a multivariable logistic regression model. We calculated the area under the receiver operating characteristic curve ( AUC) to quantify the performance of the model and the internal validity by bootstrapping. Results: Of the 101 patients included, 53 ( 52%) had persistent impaired glucose tolerance or progression to diabetes. These patients were older and more often had hypertension and used statins. A prediction model including age, current smoking, statin use, triglyceride, hypertension, previous ischemic cardiovascular disease, body mass index, and fasting plasma glucose accurately predicted persistent impaired glucose tolerance ( bootstrapped AUC,.777), with statin use, triglyceride, and fasting plasma glucose as the most important predictors. Conclusions: Half of the patients with impaired glucose tolerance after a TIA or ischemic stroke have persistent impaired glucose tolerance. We provide a prediction model to identify patients at risk of persistent impaired glucose tolerance, with statin use, triglyceride, and fasting plasma glucose as the most important predictors, which after external validation might be used to optimize secondary prevention.
引用
收藏
页码:1669 / 1675
页数:7
相关论文
共 50 条
  • [1] Prediction of Persistent Impaired Glucose Tolerance in Patients with Minor Ischemic Stroke or Transient Ischemic Attack
    Osei, Elizabeth
    den Hertog, Heleen M.
    Fonville, Susanne
    Brouwers, Paul J. A. M.
    Mulder, Laus J. M. M.
    Koudstaal, Peter J.
    Dippel, Diederik W. J.
    Zandbergen, Adrienne A. M.
    Lingsma, Hester F.
    [J]. JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, 2020, 29 (06):
  • [2] Impaired glucose tolerance increases stroke risk in nondiabetic patients with transient ischemic attack or minor ischemic stroke
    Vermeer, Sarah E.
    Sandee, Willemijn
    Algra, Ale
    Koudstaal, Peter J.
    Kappelle, L. Jaap
    Dippel, Diederik W. J.
    [J]. STROKE, 2006, 37 (06) : 1413 - 1417
  • [3] Persistent hyperfibrinogenemia in acute ischemic stroke/transient ischemic attack (TIA)
    Shenhar-Tsarfaty, Shani
    Ben Assayag, Einor
    Bova, Irena
    Shopin, Ludmila
    Cohen, Michael
    Berliner, Shlomo
    Shapira, Itzhak
    Bornstein, Natan M.
    [J]. THROMBOSIS AND HAEMOSTASIS, 2008, 99 (01) : 169 - 173
  • [4] Prevalence of abnormal glucose tolerance following a transient ischemic attack or ischemic stroke
    Kernan, WN
    Viscoli, CM
    Inzucchi, SE
    Brass, LM
    Bravata, DM
    Shulman, GI
    McVeety, JC
    [J]. ARCHIVES OF INTERNAL MEDICINE, 2005, 165 (02) : 227 - 233
  • [5] Predictors of Stroke After Transient Ischemic Attack in Children
    Lehman, Laura L.
    Watson, Christopher G.
    Kapur, Kush
    Danehy, Amy R.
    Rivkin, Michael J.
    [J]. STROKE, 2016, 47 (01) : 88 - 93
  • [6] Oral glucose tolerance test should be performed after stroke and transient ischemic attack
    Lindsberg, Perttu J.
    Tuomi, Tiinamaija
    Kaste, Markku
    [J]. INTERNATIONAL JOURNAL OF STROKE, 2011, 6 (04) : 317 - 320
  • [7] PREDICTORS FOR RETURNING TO PAID EMPLOYMENT AFTER TRANSIENT ISCHEMIC ATTACK AND MINOR ISCHEMIC STROKE
    Wicht, C.
    Chavan, C.
    Annoni, J. -M.
    Balmer, P.
    Humm, A.
    Von Roten, F. Crettaz
    Spierer, L.
    Medlin, F.
    [J]. INTERNATIONAL JOURNAL OF STROKE, 2020, 15 (1_SUPPL) : 267 - 267
  • [8] Predictors for Returning to Paid Work after Transient Ischemic Attack and Minor Ischemic Stroke
    Wicht, Corentin A.
    Chavan, Camille F.
    Annoni, Jean-Marie
    Balmer, Philippe
    Aellen, Jerome
    Humm, Andrea M.
    von Roten, Fabienne Crettaz
    Spierer, Lucas
    Medlin, Friedrich
    [J]. JOURNAL OF PERSONALIZED MEDICINE, 2022, 12 (07):
  • [9] Thrombolytic therapy for acute ischemic stroke after recent transient ischemic attack
    Alonso de Lecinana, Maria
    Fuentes, Blanca
    Masjuan, Jaime
    Simal, Patricia
    Diaz-Otero, Fernando
    Reig, Gemma
    Diez-Tejedor, Exuperio
    Gil-Nunez, Antonio
    Vivancos, Jose
    Egido, Jose-Antonio
    [J]. INTERNATIONAL JOURNAL OF STROKE, 2012, 7 (03) : 213 - 218
  • [10] Pioglitazone after Ischemic Stroke or Transient Ischemic Attack
    Kernan, W. N.
    Viscoli, C. M.
    Furie, K. L.
    Young, L. H.
    Inzucchi, S. E.
    Gorman, M.
    Guarino, P. D.
    Lovejoy, A. M.
    Peduzzi, P. N.
    Conwit, R.
    Brass, L. M.
    Schwartz, G. G.
    Adams, H. P., Jr.
    Berger, L.
    Carolei, A.
    Clark, W.
    Coull, B.
    Ford, G. A.
    Kleindorfer, D.
    O'Leary, J. R.
    Parsons, M. W.
    Ringleb, P.
    Sen, S.
    Spence, J. D.
    Tanne, D.
    Wang, D.
    Winder, T. R.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2016, 374 (14): : 1321 - 1331