Journal of Diabetes & Metabolic Disorders Category: Clinical Type: Original Article

Prevalence and Pattern of Hyperglycemia in Acute Stroke Patients in a Federal Teaching Hospital in Abakaliki Nigeria

Chukwuemeka Okorie Eze1* and Francis Chima Okoro1
1 Department of internal medicine, Neurology Unit, Alex Ekwueme Federal University Teaching Hospital, Abakaliki (AEFUTHA), Ebonyi State, Nigeria

*Corresponding Author(s):
Chukwuemeka Okorie Eze
Department Of Internal Medicine, Neurology Unit, Alex Ekwueme Federal University Teaching Hospital, Abakaliki (AEFUTHA), Ebonyi State, Nigeria
Tel:+234 7033432117,
Email:drezeconauth@yahoo.com ; drezeconauth@gmail.com

Received Date: May 23, 2024
Accepted Date: Jun 06, 2024
Published Date: Jun 13, 2024

Abstract

Background: Hyperglycemia is common in patients with acute stroke, and it is increasingly considered an independent risk factor for stroke morbidity and mortality. Admission hyperglycemia in acute stroke patients could result from diabetes mellitus or stress hyperglycemia. Despite the adverse consequences of admission hyperglycemia in acute stroke patients, there has not been any study to demonstrate the burden in Abakaliki, Nigeria. It is against this backdrop that we embarked on this cross-sectional observational hospital-based study to determine the prevalence and pattern of admission hyperglycemia in acute stroke patients in a Federal Teaching Hospital, in Abakaliki, Nigeria from November 2021 to May 2022. 

Results: Out of the 210 recruited for the study, 66 (31.4%) had admission hyperglycemia. Elevated glycated hemoglobin and right hemispheric stroke were significantly associated with hyperglycemia. 

Conclusion: Admission hyperglycemia is prevalent amongst acute stroke patients in Abakaliki, Nigeria and it is commonly associated with elevated glycated hemoglobin and right hemispheric stroke.

Introduction

Hyperglycemia is common in patients with acute stroke and occurs in up to 60% of patients overall [1-5] and approximately 12- 53% of acute stroke patients without a prior diagnosis of diabetes [6-9]. It is increasingly considered as an independent predictor of larger infarct size, poor clinical outcome, and higher risk of mortality following stroke [10]. 

Admission hyperglycemia in acute stroke patients could result from diabetes mellitus or stress Hyperglycemia and Glycated Hemoglobin (HbA1c) level is used to differentiate the two [11]. 

Diabetes mellitus is a known risk factor for stroke acting through several intermediate vascular disease risk factors, including thrombophilia, endothelial dysfunction, and inflammation [12]. HbA1c level is usually elevated in diabetes due to the long-standing presence of hyperglycemia. 

Stress hyperglycemia, also known as Claude-Bernard syndrome is common in critically ill patients like in stroke, and appears to be a marker of disease severity. It results from excessive secretion of cortisol and catecholamine’s, characterized by excessive gluconeogenesis, glycogenolysis, and insulin resistance [13-15]. HbA1c level is usually normal in stress hyperglycemia due to the short duration of the hyperglycemia. 

Prompt diagnosis and control of hyperglycemia potentially improve the outcome of stroke [16]. Despite the adverse consequences of admitting hyperglycemia to acute stroke patients, there have been few hospital-based studies of the prevalence of admitting hyperglycemia in acute stroke patients in Nigeria. It is against this backdrop that we embarked on this study on the Prevalence and pattern of admitting hyperglycemia in acute stroke patients in a Federal Teaching Hospital in Abakaliki, Nigeria. The results will form part of the database for health planning and development of stroke management protocols.

Methods

This is a cross-sectional observational hospital-based study undertaken at the Medical Emergency unit of the Alex Ekwueme Federal University Teaching Hospital Abakaliki, a tertiary hospital in Abakaliki Nigeria from November 2021 to May 2022 (7 months period). The hospital is a referral hub for Ebonyi and the surrounding states. Acute stroke (1 - 7 days post-stroke) patients usually present to the medical emergency unit from where they are admitted to either the intensive care unit or medical wards depending on the severity. All consecutive acute stroke patients that are 18 years and above, of both gender who had blood samples collected for glucose assay using Accu-check active glucometer before commencement of stroke treatment were included in the study. The case notes of the patients were used to retrieve information on the bio data, clinical characteristics, type, and location of stroke based on neuroimaging, admitting Random Blood Glucose (RBG), Glycated Hemoglobin (HbA1C), and Packed Cell Volume (PCV) test results done at presentation. Hyperglycemia was defined as RBG ≥ 140mg/dl [17]. Abnormal HbA1C was defined as ≥ 6.5% [18]. Stroke was classified as ischemic or hemorrhagic based on the findings of neuroimaging. Altered consciousness was defined as a Glasgow coma score (GCS) of < 15/15. Renal dysfunction was defined as an estimated Glomerular filtration rate (eGFR) of < 60ml/min/1.72m2 using the Modification of Diet in Renal Disease (MDRD) calculator [19]. The MDRD calculator uses Serum creatinine value, age, sex, and race in the calculation of renal function. Hypertension was defined as Systolic Blood Pressure (SBP) of ≥ 140mmHg and/or Diastolic Blood Pressure (BDP) of ≥ 90mmHg [20]. Anemia was defined as a packed cell volume (PCV) of < 36% [21]. 

The data were analyzed with Statistical Package for the Social Sciences (SPSS) version 25. The categorical variables were presented as proportions and percentages while numerical variables were presented as means and standard deviations. Chi-square was used for the test of statistical significance with a p-value of < 0.05 as significant.

Results

Two hundred and ten (male- 120, female- 90) patients who fulfilled the study criteria were recruited for the study with a sex ratio 4: 3. The age range was 32- 89 years with a mean age of 61.5 ± 12.3 years (male- 62.4 ± 12.2, female- 60.9 ± 11.8). One hundred and twenty (57%) were within the working age of 18 and 64 years old while 90 (43%) were ≥ 65 years. Sixty-six (31.4%) had hyperglycemia with no significant age and sex difference. HbA1C ≥ 6.5% and Right hemispheric stroke were significantly associated with hyperglycemia. The other details are documented in Table 1. 

Variables

Hyperglycemia

n= 66 (%)

Normoglycemia

n= 144 (%)

Total

N= 210 (%)

p-value

Sex

Male

41 (19.5)

79 (37.6)

120 (57.1)

0.4027

Female

25 (11.9)

65 (31.0)

90 (42.9)

 

Age range

(years)

18- 64

37 (17.6)

83 (39.5)

120 (57.1)

0.9486

≥ 65

29 (13.8)

61 (29.0)

90 (42.9)

 

HbA1C (%)

< 6.5

46 (21.9)

140 (66.7)

186 (88.6)

< 0.0001

≥ 6.5

20 (9.5)

4 (1.9)

24 (11.4)

 

Stroke type

Ischemic

57 (27.1)

110 (52.4)

167 (79.5)

0.1392

Hemorrhagic

9 (4.3)

34 (16.2)

43 (20.5)

 

Stroke location

Right

35 (16.7)

50 (23.8)

85 (40.5)

0.0184

Left

31 (14.8)

94 (44.8)

125 (59.5)

 

Mental status

Conscious

49 (23.3)

91 (43.3)

140 (66.6)

0.1559

Unconscious

17 (8.1)

53 (25.2)

70 (33.3)

 

Blood pressure (mmHg)

< 140/90

21 (10)

29 (13.8)

50 (23.8)

0.0949

≥ 140/90

45 (21.4)

115 (54.8)

160 (76.2)

 

Renal function

Normal

49 (23.3)

110 (52.4)

159 (75.7)

0.8702

Impaired

17 (8.1)

34 (16.2)

51 (24.3)

 

Packed cell volume (%)

≥ 36

38 (18.1)

73 (34.8)

111 (52.9)

0.3834

< 36

28 (13.3)

71 (33.8)

99 (47.1)

 

Table 1: Clinical characteristics.

Discussion

Hyperglycemia is common in patients with acute stroke, and it is increasingly considered as an independent predictor of larger infarct size, poor clinical outcome, and higher risk of mortality following stroke [10]. 

The reported prevalence of admission hyperglycemia in acute stroke patients in this study is 31.4%. It is like other hospital-based studies which reported 12- 60% [1-9]. The implication is huge considering the poor prognostic effect of hyperglycemia on acute stroke [10,22]. 

Male patients had a higher prevalence of hyperglycemia than female folks, though not statistically significant. This is similar to the report from a hospital-based study [23]. This is probably because diabetes and hyperglycemia are more prevalent in male folks than their female counterparts due to the protective role of female sex hormones [24]. 

Those in the working age group had a higher prevalence of hyperglycemia, though not statistically significant. A similar finding had been reported in the past [23]. This could result from blood glucose lowering effects of complications of diabetes like nephropathy which is more prevalent in older individuals. This finding portends great danger as the young and productive population are at risk of worse outcome following an acute stroke due to poor prognostic effects of hyperglycemia. 

Hyperglycemia had a statistically significant association with elevated HbA1C level. This is expected as HbA1C is a marker of hyperglycemia and has been recommended as a tool for the diagnosis of diabetes mellitus [18]. HbA1c is the gold standard for monitoring glycemic control in patients with diabetes mellitus and predicts the level of control over the last 8 to 12 weeks [25]. For the diagnosis of diabetes, HbA1c showed poor sensitivity and very high specificity in several studies which suggests that it should be used mainly for monitoring glycemic control, rather than for the diagnosis of diabetes [26-29]. 

Hyperglycemia was more prevalent in acute ischemic stroke than hemorrhagic stroke in this study, though not statistically significant. This is like the report of other studies [10,30]. This could have resulted from the fact that diabetes and its complications are all independent risk factors for ischemic stroke [31,32]. Furthermore, hyperglycemia also occurs in non-diabetic patients because of the acute stress responses involving the activation of the hypothalamic-pituitary-adrenal axis and the sympathetic nervous system in reaction to extensive brain injury from ischemic stroke [33]. 

Left hemispheric stroke was noted to be more prevalent than right hemispheric counterpart. This is like the report of Hedna, et al [34,35]. This hemispheric difference in frequency is due mainly to the higher incidence of left hemispheric large vessel strokes in the middle cerebral artery distribution [34]. The above is supported by intima-media complex variation and velocity differences in the left carotid artery accounting for greater stroke incidence in the left hemisphere [36]. 

The study showed that hyperglycemia was statistically more prevalent in patients that have right hemispheric stroke. There has not been any report on the difference in the prevalence of hyperglycemia between cerebral hemispheric strokes. The cause of the preponderance of hyperglycemia in patients with right hemispheric stroke may not be very clear in this study, but it could relate to the small sample size in the study. This finding should stimulate large-scale multi-center collaborative study to explore the veracity of the above finding. 

Hyperglycemia was reportedly more prevalent in patients with normal mental status. This finding may be related to the fact that hyperglycemia was also more prevalent in ischemic stroke which usually present with preserved mental status [37]. Furthermore, the patients that have normal mental status may have taken food with a high glycemic index as a first aid measure for the acute stroke symptoms. 

Hyperglycemia was more prevalent in patients with hypertension, though not statistically significant. This is like another hospital-based study [11]. The above finding could result from the fact that hypertension and hyperglycemia are components of metabolic syndrome [38]. Furthermore, both hypertension and hyperglycemia are risk factors for stroke [39]. 

Hyperglycemia was not associated with renal impairment and anemia. This is unexpected as renal impairment is reportedly associated with hypoglycemia from multi-factorial reasons which include but are not limited to deficiency of precursors of gluconeogenesis, that is, alanine, impaired glycogenolysis, diminished renal gluconeogenesis and impaired renal insulin degradation and clearance, poor nutrition, and, in a few cases, deficiency in an immediate counter regulatory hormone such as catecholamine and glucagon [40]. The explanation for the above finding is that majority of the patients with impaired renal function had mild type. The same explanation goes for anemia as renal dysfunction is mild in the majority of the patients.

Conclusion

Hyperglycemia is highly prevalent amongst acute stroke patients, and it’s associated with elevated HbA1C and right hemispheric stroke. 

There is a need for prompt screening of all acute stroke patients for hyperglycemia and then manage accordingly as it portends a poor prognosis. There is also a need for large multi-center collaborative studies to elucidate the association of hyperglycemia with right hemispheric stroke type.

Competing Interests

The authors declare that they have no competing interests.

Funding

No external support was received, rather the authors sponsored the study.

Author’s Contributions

COE conceived the study; COE and FCO were involved in the design of the study, acquisition, analysis, and interpretation of data; COE drafted the work and revised it; COE and FCO approved the submitted version (and any substantially modified version that involves the author's contribution to the study) and have agreed both to be personally accountable for the author's own contributions and to ensure that questions related to the accuracy or integrity of any part of the work, even ones in which the author was not personally involved, are appropriately investigated, resolved, and the resolution documented in the literature.

Acknowledgment

We acknowledge the staff of the medical records department for cooperation towards the retrieval of the patient’s records.

References

  1. Scott JF, Robinson GM, French JM, O’Connell JE, Alberti KG, et al. (1999) Glucose potassium insulin infusions in the treatment of acute stroke patients with mild to moderate hyperglycemia: the Glucose Insulin in Stroke Trial (GIST). Stroke 130: 793-799.
  2. van Kooten F, Hoogerbrugge N, Naarding P, Koudstaal PJ (1993) Hyperglycemia in the acute phase of stroke is not caused by stress. Stroke 24: 1129-1132.
  3. Szczudlik A, Slowik A, Turaj W, Wyrwicz-Petkow U, Pera J, et al. (2001) Transient hyperglycemia in ischemic stroke patients. Journal of the Neurological Sciences 189: 105-111.
  4. Williams LS, Rotich J, Qi R, Fineberg N, Espay A, et al. (2002) Effects of admission hyperglycemia on mortality and costs in acute ischemic stroke. Neurology 59: 67-71.
  5. Scott J, Robinson G, French J, O’Connell J, Alberti K, et al. (1999) Prevalence of admission hyperglycaemia across clinical subtypes of acute stroke. Lancet 353: 376-377.
  6. Gray CS, French JM, Bates D, Cartlidge NE, Venables GS, et al. (1989) Increasing age, diabetes mellitus and recovery from stroke. Postgrad Med J 65: 720-724.
  7. Gray CS, Taylor R, French JM, Alberti KG, Venables GS, et al. (1987) The prognostic value of stress hyperglycaemia and previously unrecognized diabetes in acute stroke. Diabetic Med 4: 237-240.
  8. Pulsinelli WA, Levy DE, Sigsbee B, Scherer P, Plum F (1983) Increased damage after ischemic stroke in patients with hyperglycemia with or without established diabetes mellitus. Am J Med 74: 540-544.
  9. Riddle M, Hart J (1982) Hyperglycemia, recognized and unrecognized, as a risk factor for stroke and transient ischemic attacks. Stroke 13: 356-359.
  10. Kruyt ND, Biessels GJ, Devries JH, Roos YB (2010) Hyperglycemia in acute ischemic stroke: pathophysiology and clinical management. Nat Rev Neurol 6: 145-155.
  11. Agabi OP, Ojo OO, Danesi MA, Ojini FI, Okubadejo NU (2021) An investigation of the relationship of the admission hyperglycemia to severity and 30-day outcome in acute ishemic and intracerebral hemorraghic stroke: A comparative cross-sectional study. J Clin Sci 18:142-147
  12. Kernan WN, Inzucchi SE, Viscoli CM, Brass LM, Bravata DM, et al. (2002) Insulin resistance and risk for stroke. Neurology 59: 809-815.
  13. Marik PE (2009) Critical illness-related corticosteroid insufficiency. Chest 135: 181-193.
  14. Chernow B, Rainey TR, Lake CR (1982) Endogenous and exogenous catecholamines in critical care medicine. Crit Care Med 10: 409-416.
  15. Dungan K, Braithwaite SS, Preiser JC (2009) Stress Hyperglycemia. Lancet 373: 1798-1807.
  16. Baker L, Juneja R, Bruno A (2011) Management of Hyperglycemia in Acute Ischemic Stroke. Curr Treat Options Neurol 13: 616.
  17. Farrokhi F, Smiley D, Umpierrez GE (2011) Glycemic control in non-diabetic critically ill patients. Best Pract Res Clin Endocrinol Metab 25: 813-824.
  18. WHO (2011) Use of Glycated Haemoglobin (HbA1c) in the Diagnosis of Diabetes Mellitus: Abbreviated Report of a WHO Consultation. Geneva: World Health Organization; 2011. 2, Glycated haemoglobin (HbA1c) for the diagnosis of diabetes. WHO, Geneva, Switzerland.
  19. Shrestha P, Thapa S, Shrestha S, Lohani S, Suresh BK, et al. (2017) Renal impairment in stroke patients: A comparison between the haemorrhagic and ischemic variants. F1000Research 6: 1531.
  20. Chobanian AV, Bakris GL, Black HR, Cushman WC, Green LA, et al. (2003) Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension 42: 1206-1252.
  21. Khalid N, Nasrullah, Iqbal RK (2019) Anaemia: Symptoms, Causes, Prevention, Diagnosis and Treatment. Clin Med Biochem 5: 146
  22. Olsen TS (2009) Blood glucose in acute stroke. Expert Rev Neurother 9: 409-419.
  23. Wahab K, Okubadejo N, Ojini F, Danesi M (2007) Effect of admission Hyperglycaemia on short-term outcome in adult Nigerians with a first acute ischaemic stroke. African Journal of Neurological Sciences 26.
  24. Tramunt B, Smati S, Grandgeorge N, Lenfant F, Arnal J, et al. (2020) Sex differences in metabolic regulation and diabetes susceptibility. Diabetologia 63: 453-461.
  25. Incani M, Sentinelli F, Perra L, Pani MG, Porcu M, et al. (2015) Glycated hemoglobin for the diagnosis of diabetes and prediabetes: Diagnostic impact on obese and lean subjects, and phenotypic characterization. J Diabetes Investig 6: 44-50.
  26. van‘t Riet E, Alssema M, Rijkelijkhuizen JM (2010) Relationship between A1C and glucose levels in the general Dutch population: the new Hoorn study. Diabetes Care 33: 61-66.
  27. Cowie CC, Rust KF, Byrd-Holt DD, Eberhardt MS, Flegal KM, et al. (2006) Prevalence of diabetes and impaired fasting glucose in adults in the U.S. population: National Health And Nutrition Examination Survey 1999–2002. Diabetes Care 29: 1263-1268.
  28. Zemlin AE, Matsha TE, Hassan MS (2011) HbA1c of 6.5% to diagnose diabetes mellitus-does it work for us? the Bellville South Africa study. PLoS One 6: 22558.
  29. Cavagnolli G, Comerlato J, Comerlato C (2011) HbA(1c) measurement for the diagnosis of diabetes: is it enough? Diabet Med 28: 31-35.
  30. Ferrari F, Moretti A, Villa RF (2022) Hyperglycemia in acute ischemic stroke: Physiopathological and therapeutic complexity. Neural Regen Res 17: 292-299.
  31. O’Donnell MJ, Xavier D, Liu L, Zhang H, Chin SL, Rao-Melacini P, et al. (2010) Risk factors for ischaemic and intracerebral haemorrhagic stroke in 22 countries (the INTERSTROKE study): a case-control study. Lancet 376: 112-123.
  32. Chen R, Ovbiagele B, Feng W (2016) Diabetes and Stroke: Epidemiology, Pathophysiology, Pharmaceuticals and Outcomes. Am J Med Sci 351: 380-386.
  33. Christensen H, Boysen G, Johannesen HH (2004) Serum-cortisol reflects severity and mortality in acute stroke. J Neurol Sci 217:175-180.
  34. Hedna VS, Bodhit AN, Ansari S, Falchook AD, Stead L, et al. (2013) Hemispheric differences in ischemic stroke: is left-hemisphere stroke more common? J Clin Neurol 9: 97-102.
  35. Kyme C (2005) Recognizing the signs of right-hemispheric stroke. Nat Rev Neurol 1: 11.
  36. Soneye MA, Adekanmi AJ, Obajimi MO, Aje A (2019) Intima-media thickness of femoral arteries and carotids among an adult hypertensive Nigerian population: A case-control study to assess their use as surrogate markers of atherosclerosis. Ann Afr Med 18: 158-166.
  37. Ojaghihaghighi S, Vahdati SS, Mikaeilpour A, Ramouz A (2017) Comparison of neurological clinical manifestation in patients with hemorrhagic and ischemic stroke. World J Emerg Med 8: 34-38.
  38. Beilby J (2004) Definition of Metabolic Syndrome: Report of the National Heart, Lung, and Blood Institute/American Heart Association Conference on Scientific Issues Related to Definition. Clin Biochem Rev 25: 195-198.
  39. Boehme AK, Esenwa C, Elkind MS (2017) Stroke Risk Factors, Genetics, and Prevention. Circ Res. 120: 472-495.
  40. Arem R (1989) Hypoglycemia associated with renal failure. Endocrinol Metab Clin North Am 18: 103-21.

Citation: Eze CO, Okoro FC (2023) Prevalence and Pattern of Hyperglycemia in Acute Stroke Patients in a Federal Teaching Hospital in Abakaliki Nigeria. J Diabetes Metab Disord 10: 045.

Copyright: © 2024  Chukwuemeka Okorie Eze, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


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