CC BY 4.0 · Libyan International Medical University Journal
DOI: 10.1055/s-0044-1779340
Original Article

Prevalence of Dyslipidemia, Drug Therapy Problems, and Medication Adherence in Type 2 Diabetes Mellitus Patients in North Central Nigeria

1   Department of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmaceutical Sciences, University of Ilorin, Ilorin, Nigeria
,
Timothy Orimogunje
1   Department of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmaceutical Sciences, University of Ilorin, Ilorin, Nigeria
,
S.I. Bello
1   Department of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmaceutical Sciences, University of Ilorin, Ilorin, Nigeria
,
2   Department of Obstetrics and Gynecology, General Hospital Ilorin, Ilorin, Nigeria
,
Muslim Olakunle Jamiu
1   Department of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmaceutical Sciences, University of Ilorin, Ilorin, Nigeria
,
Ikoni J. Ogaji
3   Department of Pharmaceutics and Pharmaceutical Technology, University of Jos, Jos, Nigeria
› Author Affiliations
Funding None.
 


Abstract

Background Patients with diabetes mellitus have an increased risk of developing dyslipidemia, predisposing them to macro- and microvascular consequences such as coronary heart disease.

Aim The aim of this study was to assess the prevalence of dyslipidemia, drug therapy problems (DTPs), and medication adherence in type 2 diabetes mellitus (T2DM) patients in a tertiary hospital in North Central Nigeria.

Method This study was a cross-sectional convenient sampling of eligible patients conducted in the General Outpatient Department of General Hospital, Ilorin, from March to May 2022. A validated questionnaire was administered to obtain all relevant information on sociodemographic information, and blood samples were collected in a medium plain heparinized tube and sent to the laboratory where fasting blood sugar, high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C) values were calculated as appropriate. Morisky's Medication Adherence Scale 8 (MMAS-8) was used to capture patient's adherence level, and DTP was assessed using the Pharmaceutical Care Network Europe (PCNE) Criteria version 7. Ethical approval was obtained from the Ministry of Health, Ilorin. Statistical Package for Social Sciences was used to analyze the data collected for descriptive and inferential statistics.

Results The mean age of the respondents was 60 ± 0.7 years. Of the 60 respondents, 25 (41.67%) were males and 35 (58.33%) were females. All the respondents had dyslipidemia, 30% respondents were identified with a DTP of nonadherence, 16.7% needed additional drug/monitoring, dosage was too low in 11.7%, and 11.6% could not afford their medication due to high cost. In all, 45 (75%) respondents had poor sugar control and 33 (55%) had poor blood pressure control. Using MMAS-8, the majority (41, [68.30%]) of the respondents were found to have poor adherence to their diabetic medications.

Conclusion High prevalence of dyslipidemia, poor medication adherence, and DTPs were found in the T2DM patients in this study.


#

Introduction

There is an irrefutable proof that diabetes mellitus increases the risk of cardiovascular disease (CVD).[1] Patients with diabetes mellitus have a two- to fourfold increased risk of dying from cardiovascular causes compared with those without diabetes.[2] Diabetes mellitus was upgraded to the highest risk group by the Adult Treatment Panel III (ATP III), which is the third report of the Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults.[3] Different dyslipidemia patterns are linked to type 2 diabetes mellitus (T2DM), predisposing patients to macrovascular consequences such coronary heart disease (CHD).[4] Moderate hypertriglyceridemia, low levels of high-density lipoprotein-cholesterol (HDL-C), and high levels of low-density lipoprotein cholesterol (LDL-C) are all components of the metabolic syndrome that is seen in people with type 2 diabetes.[5]

Dyslipidemias are brought on by metabolic disturbances, which in type 2 diabetic patients are mostly brought on by insulin resistance, which results in a malfunction in lipid metabolism. Hypertriglyceridemia, low serum HDL-C concentrations, and sporadically high serum LDL-C and lipoprotein(a) values are related with insulin resistance, relative insulin insufficiency, and obesity.[6] [7]

The risk of CHD is further increased by atherogenic dyslipidemia, hypertension, excessive plasma glucose, and prothrombotic condition, all of which are frequently linked to raised serum triglycerides.[8] With inadequate management of diabetes mellitus, glycemic control deteriorates leading to lipid and lipoprotein abnormalities; particularly total and LDL-C is raised.[9] In a study in south eastern Nigeria, the prevalence of dyslipidemia in T2DM patients was 90.7%.[10] Patients with diabetes who have suboptimal (poor) glycemic control due to poor adherence to treatment guidelines are at an increased risk of micro- and macrovascular complications, disease progression, morbidity, and death, as well as higher health care expenditures.[11] [12] Numerous reasons for nonadherence have been identified by studies, including forgetfulness, drug costs and side effects, as well as a perceived lack of benefit from ongoing therapy.[13] Drug therapy problems (DTPs) are events or circumstances involved or thought to be involved during medication administration, may actually or potentially interfere with the desired health outcomes,[14] [15] and are particularly common in diabetic patients.[16] DTPs can be divided into several groups. The Cipolle et al classification method is the most popular method of classification. DTPs can be classified into seven different categories. These are unnecessary drug therapy, need for additional drug therapy, ineffective drug therapy, dosage too low, dosage too high, adverse drug reaction, and nonadherence.[15]

There are currently no studies to collectively assess the prevalence of dyslipidemia, DTPs, medication adherence, and a 10-year risk of developing CVD in T2DM in north central Nigeria. The aim of this study was to assess the prevalence of dyslipidemia, DTPs, and medication adherence in T2DM patients attending General Hospital, Ilorin (GHI).


#

Methodology

Study Site Description

The study was conducted at General Outpatient Department (GOPD) clinic, GHI, Kwara State, Nigeria.


#

Study Design

This was a cross-sectional study among outpatients with T2DM attending the GOPD of GHI. The study was performed between March and May 2022.


#

Study Population

The patients studied were those with T2DM attending the medical outpatient ward.

Sample size determination: The minimum sample size of T2DM patients attending GOPD GHI was determined by using the statistical formula of Fisher's exact test. Thus, n  =  Z 2 pq / d 2 , where Z = standard normal deviate usually set at 1.96 corresponding to 95% confidence interval, p = proportion in the target population (T2DM with dyslipidemia) estimated to have a particular characteristic set at 96%,[17] that is, 0.96, q = 1 – p (proportion in the target population not having the particular characteristics), and d = degree of accuracy required, usually set at 0.05 level. The total sample size used in this study was 60 patients.

The inclusion criteria included male and female patients with T2DM patients who gave their consent to participate and age older than 18 years. The exclusion criteria included emergency patients and pregnant women.


#

Data Collection

Patient recruitment was done at the GOPD clinic, after their scheduled appointments with the doctors. All those who met the inclusion criteria were selected. Informed consent was obtained and patients were counseled appropriately. A validated questionnaire was administered to obtain all relevant information with section A on sociodemographic information, section B on medical and medication history, section C on Morisky's Medication Adherence Scale 8 (MMAS-8), section D on DTPs using the Pharmaceutical Care Network Europe (PCNE) Criteria Version 7 (costs of drugs too high, adherence, needs additional monitoring, dosage too high, adverse medication effect, dosage too low, unnecessary medication therapy), and section E on social history. With the help of a phlebotomist, blood samples were collected on the same day the patients were recruited, in a medium plain heparinized tube, after which the blood samples were sent to Beacon Health diagnostic center, where fasting blood sugar, HDL, and LDL values were calculated as appropriate.

Definitions: HDL-C value: less than 40 mg/dL = risk of heart disease; 41 to 59 mg/dL = good; greater than 60 mg/dL = considered protective against heart disease.

LDL-C: less than 100 mg/dL = optimal, considered protective; 100 to 129 mg/dL = above optimal; 130 to 159 mg/dL = borderline high, risk of heart disease; 160 to 189 mg/dL = high, risk of heart disease; greater than 190 = very high.

FBS: less than 7.0 mmol/L = good, controlled; greater than 7.0 mmol/L = poor, uncontrolled.

BP: less than 140 mm Hg = controlled; ≥140 mm Hg = uncontrolled.

MMAS-8: less than 6 = poor adherence; ≥6 = good adherence.[18] [19] [20]

Ten-year Framingham CVD risk score: less than 10 = low risks of developing CVD within 10 years; 10 to 20 = moderate to high risk of developing CVD within 10 years; greater than 20 = high risks of developing CVD within 10 years.[21]


#

Data Analysis

For continuous measurements such as age, the mean, median, standard deviation, and range were tabulated. For categorical measurements such as gender, the frequencies were computed. Data were analyzed using the SPSS version 25. Descriptive statistics using chi-squared test with p-value ≤0.05 was considered statistically significant.


#

Ethical Consideration

Ethical approval was obtained from the Ethical Review Committee of GHI with assigned number: GHI/ADM/134/Vol. II/420.


#
#

Results

Sociodemographic Characteristics

[Table 1] shows the sociodemographic features of the T2DM patients in this study; 41.67% of the respondents were males, while 58.33% were females, with a mean age of 60 ± 0.7 years. In all, 33.3% of the respondents had nonformal education and 54% of the respondents had low monthly income.

Table 1

Sociodemographic characteristics

Variable

Frequency, n (%)

(n = 60)

Gender

Male

25 (41.67)

Female

35 (58.33)

Age (y)

35–45

6 (10.0)

46–50

4 (6.67)

51–55

10 (16.67)

56–60

8 (13.33)

61–65

10 (16.67)

66–70

17 (28.33

>70

5 (8.33)

Mean age (y)

60 ± 0.7

Residence

Urban

25 (41.65)

Rural

35 (58.33)

Highest educational qualification

Nonformal

20 (33.33)

Primary

17 (28.33)

SSCE

16 (26.67)

Tertiary

5 (8.33)

Adult education

1 (1.67)

Marital status

Single

1 (1.67)

Married

54 (90.00)

Divorced

5 (8.33)

Religion

Islam

39 (65.00)

Christianity

19 (31.67)

Traditional

2 (3.33)

Monthly income

Low

32 (54.00)

Medium

20 (33.00)

High

8 (13.00)

Abbreviation: SSCE, Senior Secondary Certificate Examination.



#

Prevalence of Dyslipidemia, Clinical, and Biochemical/Metabolic Variables among Respondents

The prevalence of dyslipidemia in this study was 100% ([Table 2]). In total, 95% had a single dyslipidemia (i.e., at least one abnormal lipid fraction with either high LDL-C or low HDL-C), while 5% had multiple dyslipidemias (both high LDL-C and low HDL-C). In all, 81.67% (49.0) of the respondents had a good HDL value, which is considered to be protective against CVDs. Thirty patients (50%) had a high LDL-C value, which is considered to be a major risk factor for developing CVD. Forty-five (75.0%) respondents had poor FBS levels, while 15 (25.0%) had good sugar control. Thirty-three (55%) respondents had poor BP control ([Table 2]).

Table 2

Prevalence of dyslipidemia, clinical, and biochemical/metabolic variables among respondents

Frequency (n = 60)

Percentage

Dyslipidemia

Single

57

95.00

Multiple

3

5.00

Total

60

100.00

HDL (mg/dL)

<40

4

6.67

41–59

7

11.67

>60

49

81.67

Total

60

100.00

LDL (mg/dL)

<100

30

50.00

100–129

2

3.30

130–159

7

11.70

160–189

9

15.00

>190

12

20.00

Total

60

100.00

FBS (mmol/L)

<7.0

15

25.00

≥7.0

45

75.00

Systolic BP (mm Hg)

<140

27

45

≥140

33

55

Total

60

100

Abbreviations: BP, blood pressure; FBS, fasting blood sugar level; HDL, high-density lipoprotein; LDL, low-density lipoprotein.



#

Distribution of Dyslipidemia Based on Gender and Socioeconomic Status among Respondents

As can be seen from the results shown in [Table 3], there was no association between dyslipidemia and gender, level of education, area of residence, or socioeconomic status (p > 0.05).

Table 3

Distribution of dyslipidemia based on gender, socioeconomic status among respondents

Variables

Dyslipidemia

Total

χ 2

p-value

Single

Multiple

Gender

 Male

25

0

25

2.26

0.13

 Female

32

3

35

Level of education

 Nonformal

20

0

20

8.68

0.06

 Primary

17

0

17

 SSCE

13

3

16

 Tertiary

6

0

0

 Adult education

1

0

1

Residence

 Rural

32

3

35

2.26

0.13

 Urban

25

0

25

Monthly income

 Low

31

1

32

1.71

0.42

 Medium

18

2

20

 High

8

0

0

Abbreviation: SSCE, Senior Secondary Certificate Examination.



#

Drug Therapy Problem and MMAS-8 among Respondents

Using the PCNE DTP classification ([Table 4]), the majority of the respondents (30%) were nonadherent to their medications, 16.7% (10.0) of the respondents needed additional drug/monitoring, 11.7% had dosage too low, 11.6% could not afford their medication due to high cost, and 6.70% (4.0) had an unnecessary medication therapy. Further using the MMAS-8 to class respondent as having good adherence or poor adherence, 31.7% (19) of the respondents had good adherence, while 68.30% (41) of the respondents had poor adherence to their diabetic medications.

Table 4

Drug therapy problem and MMAS-8 among respondents

Drug therapy problem

Frequency (%)

(n = 60)

Costs

11.60

Adherence

30.00

Needs additional monitoring

16.70

Dosage too high

8.30

Adverse medication effect

15.00

Dosage too low

11.70

Unnecessary medication therapy

6.70

MMAS-8

Frequency ( n  = 60)

Percentage

<6

41

68.30

≥6

19

31.70

Total

60

100.00

Notes: <6 = poor adherence; ≥6 = good adherence.


The MMAS-8, content, name, and trademarks are protected by U.S. copyright and trademark laws. Permission for use of the scale and its coding is required. A license agreement is available from MMAR, LLC., www.moriskyscale.com.


The 10-year Framingham risk score (FRS) for CVD, distribution of the 10-year FRS for CVD based on gender among respondents, and the correlation between the 10 years FRS for CVD, and MMAS-8 among respondents are shown in [Table 5].

Table 5

Ten-year Framingham risk score (FRS) for CVD, distribution of 10-year FRS for CVD based on gender, and correlation between 10-year FRS for CVD and MMAS-8 adherence score among respondents

CVD risk scores

Frequency ( n  = 60)

Percentage

 < 10

14

23.30

 10–20

16

26.70

 > 20

30

50.00

 otal

60

100.00

CVD risk score

Gender

Total ( N  = 60)

χ 2

p -value

Male

Female

  < 10

7

7

14

10.3

0.0057

 10–20

15

10

15

  > 20

3

18

21

 Total

25

35

60

CVD risk score

MMAS-8 <6

MMAS-8 ≥6

Total ( N  = 60)

χ 2

p -value

  < 10

12

2

14

6.2

0.04

 10–20

9

7

16

  > 20

26

4

30

 Total

47

13

60

Abbreviations: CVD, cardiovascular disease; MMAS-8, Morisky Medication Adherence Scale 8.


Notes: FRS: <10 = low risk of developing CVD; 10–20 = moderate high of developing CVD; >20 = high risk of developing CVD).


MMAS: <6 = poor adherence; >6 = good adherence.


MMAS-8, content, name, and trademarks are protected by U.S. copyright and trademark laws. Permission for use of the scale and its coding is required. A license agreement is available from MMAR, LLC., www.moriskyscale.com.


Fifty percent (30) of the respondents had a high risk of developing CVD (stroke, heart failure, angina, etc.) within 10 years, 26.7% (16) of the respondents had moderate risk of developing CVD within 10 years, and 23.3% (14) of the respondents had low risk of CVD. Based on gender, female patients had a higher CVD risk compared with their male counterparts (p < 0.05). There is also a statistical significance in relation to the risks of CVD and adherence (p <0.05; [Table 5]).


#
#

Discussion

In this study, 41.67% (25) of the patients with T2DM were males and 58.33% (35) were females, similar to several studies[5] [10] [22] that showed that diabetes mellitus was more prevalent in females than in males. The prevalence of dyslipidemia in T2DM was high in this study (100%) with 95% having single dyslipidemia and 5% having multiple dyslipidemias. Our results appeared relatively higher compared with other studies in Nigeria that report a prevalence of 90.7%[10] and in south Africa[23] that report a prevalence of in 90.3%, with 24% having a single dyslipidemia and 66.6% having multiple dyslipidemias.[10] This can be partially explained by the poor glycemic control seen in respondents, where the hypercholesterolemia was hypothesized to be caused by an increase in non enzymatic glycation of LDL.[24] Lack of insulin prevents LDL cholesterol from being degraded by a reduction in LDL receptor binding, which raises LDL cholesterol levels.[25]

The most common lipid abnormality in this study was a high LDL-C (50%), while low HDL-C was found in only 6.67% patients. This is in contrast to several studies in Nigeria[10] [26] that showed low HDL-C as the predominant lipid abnormality. Our study also found dyslipidemia to occur more frequently in women than in men (32, 53.3%). A meta-analysis of hypercholesterolemia in Nigeria showed a slightly higher rate in women than in men. This higher rate may be due to physical inactivities and increasing patronage of processed foods. The reports show that women adopt this lifestyle to increase weight as they erroneously think that a higher weight indicates a better living standard and higher social class.[27] The assessment of DTP was solely by review of the medical and biochemical parameters. The DTP identified in this study was dosage too low in 11.7% respondents, 11.6% respondents could not purchase their medications due to high costs, 15% experienced adverse effects with their medications, 16.7% needed additional monitoring, while 30% were not adherent with their medications. In contrast Zaman Huri et al reported drug choice problem (26.1%) as the most common DTP experienced in T2DM patients with dyslipidemia, followed by potential drug interaction (18%), dosing problem (14.3%), and drug use problem (14.3%).[28] Several studies also show DM patients to be nonadherent to their medications. The MMAS-8,[18] [19] [20] which has a sensitivity of 93% and is used to identify patients with poor adherence to their medications, was used in this study. It was found that 68.30% respondents were nonadherent to their medications. In contrast, Jemal et al, while using a four-item Morisky scale, reported 70.4% adherence and 29.6% nonadherence.[29] Adherence to medication is crucial to decrease micro- and macrovascular complications in hypertension and DM patients as nonadherence can cause dyslipidemia and higher HbA1c levels,[30] stroke, heart failure, and kidney dysfunction, leading to morbidity and mortality. Several studies have linked lower socioeconomic status with nonadherence.[30]

The FRS, a common and simplified tool used to assess the risks of developing coronary artery diseases within 10 years, was used in this study with six FRS coronary risk scores: age, gender, low HDL-C, high LDL-C, high systolic blood pressure, and presence of diabetes.[21] Fifty percent of the respondents had a high risk of developing CVD (stroke, angina, etc.) within 10 years, while the chi-squared test showed that the females had a higher risk of CVD when compared with males (p < 0.05) and the chi-square test also showed that lower adherence to medication increases the risk of CVD. Identifying men and women at higher risk of future cardiovascular events can be helpful for physicians and patients to decide whether lifestyle adjustment and preventive medical care are necessary, as well as for patient education.[21]


#

Conclusion

The study revealed a high prevalence of dyslipidemia, DTPs, and medication nonadherence. All the respondents had high LDL-C, low HDL-C, or both. Multiple DTPs were identified, including nonadherence, need for additional drug/monitoring, low dosage, and inability to afford medication due to high cost. The majority of patients had poor sugar and blood pressure control. According to MMAS-8, most respondents had poor adherence to their diabetic medications, and half of the respondents were at high risk of developing CVD within 10 years.


#
#

Conflict of Interest

None declared.

  • References

  • 1 Chahil TJ, Ginsberg HN. Diabetic dyslipidemia. Endocrinol Metab Clin North Am 2006; 35 (03) 491-510 , vii–viii
  • 2 Centers for Disease Control and Prevention. National diabetes fact sheet. 2011 Accessed November 20, 2022 at: http://www.cdc.gov/diabetes/pubs/pdf/ndfs_2011.pdf
  • 3 National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report. Circulation 2002; 106: 3143-3421
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  • 5 Naheed T, Khan A, Masood G, Yunus BB, Chaudry MA. Dyslipidemias in type II diabetes mellitus patients in a teaching hospital of Lahore, Pakistan. Pak J Med 2003; 19 (04) 283-286
  • 6 Garg A, Grundy SM. Management of dyslipidemia in NIDDM. Diabetes Care 1990; 13 (02) 153-169
  • 7 O'Brien T, Nguyen TT, Zimmerman BR. Hyperlipidemia and diabetes mellitus. Mayo Clin Proc 1998; 73 (10) 969-976
  • 8 Ginsberg HN. Identification and treatment of hypertriglyceridemia as a risk factor for coronary heart disease. Curr Cardiol Rep 1999; 1 (03) 233-237
  • 9 Grundy SM. Hypertriglyceridemia, insulin resistance, and the metabolic syndrome. Am J Cardiol 1999; 83 (9B): 25F-29F
  • 10 Jisieike-Onuigbo NN, Unuigbe EI, Oguejiofor CO. Dyslipidemias in type 2 diabetes mellitus patients in Nnewi South-East Nigeria. Ann Afr Med 2011; 10 (04) 285-289
  • 11 Pladevall M, Williams LK, Potts LA, Divine G, Xi H, Lafata JE. Clinical outcomes and adherence to medications measured by claims data in patients with diabetes. Diabetes Care 2004; 27 (12) 2800-2805
  • 12 Krapek K, King K, Warren SS. et al. Medication adherence and associated hemoglobin A1c in type 2 diabetes. Ann Pharmacother 2004; 38 (09) 1357-1362
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  • 17 Basit A, Sabir S, Riaz M, Fawwad A. NDSP members. NDSP 05: Prevalence and pattern of dyslipidemia in urban and rural areas of Pakistan; a sub analysis from second National Diabetes Survey of Pakistan (NDSP) 2016-2017. J Diabetes Metab Disord 2020; 19 (02) 1215-1225
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  • 29 Jemal A, Abdela J, Sisay M. Adherence to oral antidiabetic medications among type 2 diabetic (T2DM) patients in Chronic Ambulatory Wards of Hiwot Fana Specialized University Hospital, Harar, Eastern Ethiopia: a cross sectional study. J Diabetes Metab 2017; 8 (01) 8-40
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Address for correspondence

F.O. Aliyu
Department of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmaceutical Sciences, University of Ilorin
Ilorin
Nigeria   

Publication History

Article published online:
16 February 2024

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  • References

  • 1 Chahil TJ, Ginsberg HN. Diabetic dyslipidemia. Endocrinol Metab Clin North Am 2006; 35 (03) 491-510 , vii–viii
  • 2 Centers for Disease Control and Prevention. National diabetes fact sheet. 2011 Accessed November 20, 2022 at: http://www.cdc.gov/diabetes/pubs/pdf/ndfs_2011.pdf
  • 3 National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report. Circulation 2002; 106: 3143-3421
  • 4 Betteridge DJ. Diabetic dyslipidaemia. Diabetes Obes Metab 2000; 2 (Suppl. 01) S31-S36
  • 5 Naheed T, Khan A, Masood G, Yunus BB, Chaudry MA. Dyslipidemias in type II diabetes mellitus patients in a teaching hospital of Lahore, Pakistan. Pak J Med 2003; 19 (04) 283-286
  • 6 Garg A, Grundy SM. Management of dyslipidemia in NIDDM. Diabetes Care 1990; 13 (02) 153-169
  • 7 O'Brien T, Nguyen TT, Zimmerman BR. Hyperlipidemia and diabetes mellitus. Mayo Clin Proc 1998; 73 (10) 969-976
  • 8 Ginsberg HN. Identification and treatment of hypertriglyceridemia as a risk factor for coronary heart disease. Curr Cardiol Rep 1999; 1 (03) 233-237
  • 9 Grundy SM. Hypertriglyceridemia, insulin resistance, and the metabolic syndrome. Am J Cardiol 1999; 83 (9B): 25F-29F
  • 10 Jisieike-Onuigbo NN, Unuigbe EI, Oguejiofor CO. Dyslipidemias in type 2 diabetes mellitus patients in Nnewi South-East Nigeria. Ann Afr Med 2011; 10 (04) 285-289
  • 11 Pladevall M, Williams LK, Potts LA, Divine G, Xi H, Lafata JE. Clinical outcomes and adherence to medications measured by claims data in patients with diabetes. Diabetes Care 2004; 27 (12) 2800-2805
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