Research Article - (2026) Volume 11, Issue 1
Prevalence of Diabetic Nephropathy Among Diabetic Patients in Al_Wahda Hospitals, Yemen
Received Date: Feb 03, 2026 / Accepted Date: Mar 10, 2026 / Published Date: Mar 18, 2026
Copyright: ©2026 Mohammed Ali Al-Madwami, 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.
Citation: Salah, M. K., Al-Madwami, M. A., Ali-Obaid, E. Y., Al-jabri, S. M. A. (2026). Prevalence of Diabetic Nephropathy Among Diabetic Patients in Al_Wahda Hospitals, Yemen. Int J Diabetes Metab Disord, 11(1), 01-09.
Abstract
Background: Diabetic nephropathy (DN) is a serious microvascular complication of diabetes mellitus, leading to significant morbidity and mortality. Its early detection is crucial for preventing progression.
Objective: This study aimed to determine the prevalence of DN and identify associated demographic and clinical factors among diabetic patients at Al-Wahda Hospitals/ in Dhamar, Yemen.
Methods: A retrospective, cross-sectional study was conducted on 110 diabetic patients. Data on demographics, clinical parameters (including HbA1c, blood pressure) and Albumin-to-Creatinine Ratio (ACR)were collected from medical records. DN was defined by ACR categories: normal (<30mg/g), microalbuminuria (30-300 mg/g) and macroalbuminuria (>300mg/g).
Results: The prevalence of DN (microalbuminuria and macroalbuminuria) was 80%. Microalbuminuria was present in 62.7% of patients, while macroalbuminuria was found in17.3%.Key factors significantly associated with DN included longer duration of diabetes (>10 years), poor glycemic control (HbA1c ≥6.5%, 71.8% of patients),and the presence of hypertension (30.9%).A striking diagnostic gap was observed,with only 9.1% of patients having a formal clinical diagnosis of nephropathy despite the high biochemical prevalence. Urine dipstick testing showed poor sensitivity for early detection compared to quantitative ACR.
Conclusion: There is a high, under-diagnosed burden of DN among diabetic patients in this setting. The findings underscore the critical need for implementing routine quantitative ACR screening, strict control of glycemia and blood pressure, and enhancing patient follow-up to enable early intervention and slow disease progression.
Keywords
Diabetic Nephropathy, Diabetes Mellitus, Albumin-to-Creatinine Ratio, Microalbuminuria, Chronic Kidney Disease, HbA1c, Hypertension, Type 2 Diabetes Mellitus, Urine Dipstick Test, Disease Duration.Introduction
Diabetes mellitus (DM), commonly known as diabetes refers to a group of chronic systemic non-communicable diseases characterized by abnormally high blood glucose levels termed as hyperglycemia caused due to the resistance and lack of insulin production, or uncontrolled glucagon secretion [1-3]. Being one of the top 10 causes of global mortality, diabetes has turned into a global epidemic and a massive threat to public health with an estimated number of 451 million adult patients worldwide in 2017 which may rise to 693 million by 2045 if no worthwhile preventive actions are taken immediately [4,5]. According to National Diabetes Statistics Report, 2022, more than 37 million United States adults are currently living with diabetes and 1 in every 5 of them are unaware of having it [6]. Diabetes is the eighth leading cause of mortality and the leading cause of end-stage renal disease (ESRD) and renal failure, lower-limb amputations, and adult blindness in the United States of America (USA) [7].
Type 1 and type 2 are the 2 most common types of DM although some other categories including maturity-onset diabetes of the young, gestational diabetes mellitus, neonatal diabetes, and secondary diabetes resulting from endocrine disease or hereditary diseases or medications such as corticosteroids, thiazide diuretics, beta-blockers, antipsychotics, statins, etc [8-10]. Type 1 DM, also known as juvenile diabetes or insulin-dependent diabetes mellitus is caused due to insulin deficiency resulting from the death of pancreatic beta-cells and type 2 DM or non-insulin-dependent diabetes mellitus, which is far more prevalent, is largely the result of gradually poor glucose regulation caused by a combination of malfunctioning pancreatic beta cells and insulin resistance [11,12]. Type 1 DM is expected to afflict children and adolescents, but type 2 DM is thought to affect middle-aged and older individuals who have chronic hyperglycemia as a result of poor lifestyle and nutritional factors [13,14]. Persistent hyperglycemia due to type 1 and type 2 DM affects the vascular system and induces diabetic vascular complications including microvascular complications such as diabetic nephropathy, neuropathy, and retinopathy as well as macrovascular complications such as ischemic heart disease, coronary artery disease, peripheral vascular disease, and cerebrovascular disease leading to organ damage and failure in approximately one third to one-half of people living with diabetes [15-17].
Nephropathy is a serious consequence of DM that has a substantial impact on communities worldwide [18]. It is a disorder characterized by chronic albuminuria, decline in glomerular filtration rate, and elevated arterial blood pressure leading to progressive decline of kidney function and increased cardiovascular morbidity and mortality among 20% to 40% of people with type 1 and type 2 DM [19-21]. The occurrence of nephropathy has increased along with the prevalence of diabetes [22]. The association between hemodynamic and metabolic pathways, that are commonly disrupted in the setting of diabetes, are likely to have a role in the initiation and progression of nephropathy [23]. Nephropathy is a significant microvascular consequence of diabetes along with a high prevalence, mortality, and treatment expense, yet it is poorly understood and treated. The primary cause of the problem is a lack of early detection and effective treatment therapy and strategy [24]. Also, the pathophysiological development of nephropathy is significantly influenced by poor glycemic management, hyperlipidemia, smoking, oxidative stress, accumulation of advanced glycation end products, and environmental, genetic, and epigenetic variables [25]. Effective measures to reduce the risks of nephropathy or to slow down the progression include proper monitoring and control of blood glucose levels and hypertension either by doing physical exercise and maintaining a healthy diet and lifestyle or by taking blood glucose-lowering agents for glycemic control and antihypertensive drugs [26].
Nephropathy among diabetic patients is the leading cause of dialysis in many nations, including, Western regions, Asians, and Caucasians [17]. Diabetic complications, particularly renal disease, significantly raise the chance of severe illness and death among diabetic patients. The number of cases of nephropathy in diabetic patients continues to rise significantly along with its associated mortality and cardiovascular consequences [27]. Diabetes-associated nephropathy, the primary cause of chronic kidney disease has been found to be increased in overall Europe and countries of the other continents such as Japan and Nigeria as well [28,29]. Nephropathy-associated end-stage renal failure poses a significant health problem for the people living with diabetes besides their families and healthcare systems in both high and middle-income nations due to the uprising prevalence of diabetes worldwide [23].
Objective
The aim of this study is to find out the prevalence of diabetic nephropathy among diabetic patient in AL_WAHDA hospitals.
i. To determine the prevalence of diabetic nephropathy among diabetes.
ii. To identify demographic and clinical factors.associated with an increased risk of diabetic nephropathy.
Materials and Methods
Study Area and Setting
This study will be conducted at AL_WAHDA hospitals Dhamar Governorate, Yemen.
Study Design
This is retrospective, cross-sectional hospital-based study to findings diabetic patient with diabetic nephropathy in AL_WAHDA hospitals Dhamar Governorate, Yemen.
Study Population
This study will target the patients according to:
• Included Criteria: patient with a confirmed diagnosis of type 1 or type 2 diabetes.
• Excluded Criteria: patient with incomplete medical records or those with acute kidney injury.
Data Collection
The data will be collected using medical files for diabetic patient in Al_WAHDA hospitals
• Demographic Data: age, sex, ethnicity, special habitus and duration
• Clinical data: blood pressure, HbA1c, albumin /creatinine ratio, urine dipstick test and lipid profiles.
Statistical Analysis
Statistical package for social science (spss) will be used for data entry and analysis on. Data will be represented as finding on .Also on descriptive statistic in frequency and percentage for nominal variable and mean SD for continuous variable.
Sample Size
Based on preliminary data and the desired confidence intervals, calculate a sample size needed to detect the expected prevalence rate.
Ethical Consideration
• Obtain informed consent from all participants*.
• Ensure confidentiality and anonymity of patient*
Result
General (socio-demographic) characteristics of diabetic Patient's participation in this study (n=110)
As shown in Table 1, the most participation age group with diabetic nephropathy risk was adult patients, especially those aged 41-50 and >60 years, constituting 39.1% and 32.7% of the sample, respectively.
|
Age |
<30 mg/g |
30-300 mg/g |
>300 mg/g |
Total |
|
Under 20yrs |
0 (0.0%) |
1 (0.9%) |
0 (0.0%) |
1 (0.9%) |
|
21-30yrs |
0 (0.0%) |
2 (1.8%) |
3 (2.7%) |
5 (4.5%) |
|
31-40yrs |
4 (3.6%) |
9 (8.2%) |
1 (0.9%) |
14 (12.7%) |
|
41-50yrs |
12 (10.9%) |
26 (23.6%) |
5 (4.5%) |
43 (39.1%) |
|
51-60yrs |
0 (0.0%) |
8 (7.3%) |
3 (2.7%) |
11 (10.0%) |
|
More than 60yrs |
6 (5.5%) |
23 (20.9%) |
7 (6.4%) |
36 (32.7%) |
|
Total |
22 (20.0%) |
69 (62.7%) |
19 (17.3%) |
110 (100%) |
Table 1: Distribution of Patients by Age Group and Albumin-to-Creatinine Ratio (ACR) Category (n=110)
General (socio-demographic) characteristics of diabetic Patient's participation in this study (n=110)
According to Table 2, males (50.9%) and females (49.1%) were almost equally represented. Microalbuminuria was the predominant abnormality in both genders (30.9% in males, 31.8% in females). However, macroalbuminuria was slightly higher in males compared to females (5.5%). This indicates a marginally higher risk of advanced (11.8%) nephropathy among male patients.
|
Gender |
<30 mg/g |
30-300 mg/g |
>300 mg/g |
Total |
|
Male |
9 (8.2%) |
34 (30.9%) |
13 (11.8%) |
56 (50.9%) |
|
Female |
13 (11.8%) |
35 (31.8%) |
6 (5.5%) |
54 (49.1%) |
|
Total |
22 (20.0%) |
69 (62.7%) |
19 (17.3%) |
110 (100%) |
Table 2: Distribution of Patients by Gender and Albumin-to-Creatinine Ratio (ACR) Category
Table 3: Association between Duration of Diabetes and ACR of diabetic patients’ participation in this study (n=110)
As presented in Table 3, longer duration of diabetes was associated with higher prevalence of albuminuria. Patients with >10years of diabetes showed the highest rates of macroalbuminuria (9.1%), compared to 0% among those with <1year of disease Microalbuminuria was most common in patients with 1-5years (25.5%) and >10years These findings confirm that diabetic kidney disease risk increases progressively (13.6%) with disease duration
|
Duration |
<30 mg/g |
30-300 mg/g |
>300 mg/g |
Total |
|
<1 year |
11 (10%) |
11 (10%) |
0 (0.0%) |
22 (20%) |
|
1-5 years |
6 (5.5%) |
28 (25.5%) |
4 (3.6%) |
38 (34.5%) |
|
6-10 years |
3 (2.7%) |
15 (13.6%) |
5 (4.5%) |
23 (20.9%) |
|
≥10 years |
2 (1.8%) |
15 (13.6%) |
10 (9.1%) |
27 (24.5%) |
|
Total |
22 (20%) |
69 (62.7%) |
19 (17.3%) |
110 (100%) |
Table 3: Association between Duration of Diabetes and Albumin-to-Creatinine Ratio (ACR)
Category In Table 4 Association between Type of Diabetes and ACR of diabetic Patient's participation in this study (n=110)
According to Table 4, Type II diabetes accounted for the majority of cases (92.7%). Both microalbuminuria (59.1%) and macroalbuminuria (14.5%) were more prevalent in TypeII compared to Type I (3.6% and 2.7%, respectively).This indicates that Type II diabetes patient's are at significantly higher risk of nephropathy than Type I patients.
|
Type |
<30 mg/g |
30-300 mg/g |
>300 mg/g |
Total |
|
Type I |
1 (0.9%) |
4 (3.6%) |
3 (2.7%) |
8 (7.3%) |
|
Type II |
21 (19.1%) |
65 (59.1%) |
16 (14.5%) |
102 (92.7%) |
|
Total |
22 (20%) |
69 (62.7%) |
19 (17.3%) |
110 (100%) |
Table 4: Association between Type of Diabetes and Albumin-to-Creatinine Ratio (ACR) Category
Table 5: Association between Treatment Regimen and ACR of diabetic patient's participation in this study (n=110)
As shown in Table 5, most patients were managed with or almedication plus diet/lifestyle modifications (76.4%). Within this group, microalbuminuria was most common (45.5%) and macroalbuminuria was also substantial(13.6%). Patient's on insulin only showed a relatively high prevalence of macroalbuminuria (1.8%), despite their smaller proportion. This suggests that patients requiring insulin may represent those with more advanced disease and thus higher nephropathy risk.
|
Treatment Regimen |
<30 mg/g |
30-300 mg/g |
>300 mg/g |
Total |
|
Oral Medication Only |
1 (0.9%) |
6 (5.5%) |
0 (0.0%) |
7 (6.4%) |
|
Insulin Only |
0 (0.0%) |
1 (0.9%) |
2 (1.8%) |
3 (2.7%) |
|
Diet & Lifestyle Only |
0 (0.0%) |
1 (0.9%) |
0 (0.0%) |
1 (0.9%) |
|
Oral + Insulin |
1 (0.9%) |
5 (4.5%) |
2 (1.8%) |
8 (7.3%) |
|
Oral + Diet/Lifestyle |
19 (17.3%) |
50 (45.5%) |
15 (13.6%) |
84 (76.4%) |
|
Oral + Insulin + Diet / Lifestyle |
1 (0.9%) |
6 (5.5%) |
0 (0.0%) |
7 (6.4%) |
|
Total |
22 (20%) |
69 (62.7%) |
19 (17.3%) |
110 (100%) |
Table 5: Association between Treatment Regimen and Albumin-to-Creatinine Ratio (ACR) Category
Table 6: Association between Patient-Reported Symptoms and ACR of diabetic patients’ participation in this study (n=110)
According to Table 6, common symptoms included swelling of feet/ankles (14.5% nocturia (23.6%), foamy urine (4.5%), fatigue (50.9%), and loss of appetite (30%). Fatigue, and nocturia (15.5%) were especially associated with microalbuminuria. Notably (31.8%) of patients reported no symptoms, high lighting the silent progression of diabetic nephropathy (30%) and the importance of routine screening.
Table 6 association between patient-rpeported symptoms and albumin-to-creatine ratio ratio (ACR) Category.
|
Symptoms |
Symptom |
<30 mg |
30-300 mg |
>300 mg |
Total |
|
Swelling in feet/ ankle |
(Yes) |
5 (4.5%) |
10 (9.1%) |
1 (0.9%) |
16(14.5%) |
|
(No) |
17 (15.5%) |
59 (53.6%) |
18 (16.4%) |
94(85.5%) |
|
|
|
|
|
|
|
|
|
Nocturia |
(Yes) |
5 (4.5%) |
16 (14.5%) |
5 (4.5%) |
26(23.6%) |
|
(No) |
17 (15.5%) |
53 (48.2%) |
14 (12.7%) |
84(76.4%) |
|
|
|
|
|
|
|
|
|
Foamy urine |
(Yes) |
2 (1.02%) |
3 (2.7%) |
0 (0.0%) |
5(4.5%) |
|
(No) |
20 (18.2%) |
66 (60%) |
19 (17.3%) |
105(95.5%) |
|
|
Frequent urination |
(Yes) |
6 (5.5%) |
12 (10.9%) |
2 (1.02%) |
20(18.2%) |
|
|
(No) |
16 (14.6%) |
57 (51.8%) |
17 (15.5%) |
90(81.8%) |
|
|
|
|
|
|
|
|
Fatigue |
(Yes) |
11 (10%) |
35 (31.8%) |
10 (9.1%) |
56(50.9%) |
|
(No) |
11 (10%) |
34 (30.9%) |
9 (8.2%) |
54(49.1%) |
|
|
Nausea |
(Yes) |
0 (0.0%) |
4 (3.6%) |
1 (0.9%) |
5(4.5%) |
|
(No) |
22 (20%) |
65 (59.1%) |
18 (16.4%) |
105(95.5%) |
|
|
Loss of appetite |
(Yes) |
9 (8.2%) |
17 (15.5%) |
7 (6.4%) |
33(30%) |
|
(No) |
13 (11.8%) |
52 (47.3%) |
12 (10.9%) |
77(70%) |
|
|
Increased thirst |
(Yes) |
4 (3.6%) |
14 (12.7%) |
5 (4.5%) |
23(20.9%) |
|
(No) |
18 (16.4%) |
55 (50%) |
14 (12.7%) |
87(79.1%) |
|
|
No symptoms |
(Yes) |
6 (5.5%) |
22 (20%) |
5 (4.5%) |
33(30%) |
|
(No) |
16 (14.6%) |
47 (42.7%) |
14 (12.7%) |
77(70%) |
Table 6: Association between Clinical Diagnosis of Nephropathy and ACR of diabetic patient's participation in this study (n=110)
As presented in Table 6 (second), only 9.1% of patients had a formal clinical diagnosis of nephropathy, despite higher proportions showing albuminuria (62.7%with microalbuminuria and 17.3% with macroalbuminuria). This indicates a significant gap between clinical recognition and early biochemical detection of nephropathy.
Table 6 Association between Clinical Diagnosis of Nephropathy and Albumin-to-Creatinine Ratio (ACR) Category.
|
Nephropathy |
<30 mg/g |
30-300 mg/g |
>300 mg/g |
Total |
|
Yes |
1 (0.9%) |
6 (5.5%) |
3 (2.7%) |
10 (9.1%) |
|
No |
21 (19.1%) |
63 (57.3%) |
16 (14.5%) |
100 (90.9%) |
|
Total |
22 (20%) |
69 (62.7%) |
19 (17.3%) |
110 (100%) |
Table 6 (second): Association between Time since Last Healthcare Visit and ACR of diabetic patient's participation in this study (n=110)
According to Table 7, patients with more recent healthcare visits (<3months) were more likely to have normal ACR (16.4%) compared to those with >1year since their last visit Conversely, macroalbuminuria was more prevalent in those who delayed. (0.9%) healthcare visits >1year (7.3%). This underscores the importance of regular medical follow-up in preventing progression of diabetic kidney disease.
|
Last Visit |
<30 mg/g |
30-300 mg/g |
>300 mg/g |
Total |
|
<3 months |
18 (16.4%) |
36 (32.7%) |
6 (5.5%) |
60 (54.5%) |
|
3-6 months |
3 (2.7%) |
15 (13.6%) |
4 (3.6%) |
22 (20.0%) |
|
6 months-1 year |
0 (0.0%) |
4 (3.6%) |
1 (0.9%) |
5 (4.5%) |
|
≥1 year |
1 (0.9%) |
14 (12.7%) |
8 (7.3%) |
23 (20.9%) |
|
Total |
22 (20%) |
69 (62.7%) |
19 (17.3%) |
110 (100%) |
Table 7: Association between Time since Last Healthcare Visit and Albumin-to-Creatinine Ratio (ACR) Category
Table 8: Association between Hypertension and ACR of diabetic patient's participation in this study (n=110).
As shown in Table 8, hypertension was present in 30.9% of participants. Among these macroalbuminuria was observed in 7.3% compared to 10% in non-hypertensives. However, microalbuminuria was higher in hypertensives (20%) compared to non hypertensives (42.7%). This suggests that hypertension is an important comorbidity contributing to early nephropathy.
|
Hypertension |
<30 mg/g |
30-300 mg/g |
>300 mg/g |
Total |
|
Yes |
4 (3.6%) |
22 (20.0%) |
8 (7.3%) |
34 (30.9%) |
|
No |
18 (16.4%) |
47 (42.7%) |
11 (10.0%) |
76 (69.1%) |
|
Total |
22 (20%) |
69 (62.7%) |
19 (17.3%) |
110 (100%) |
Table 8: Association between Hypertension and Albumin-to-Creatinine Ratio (ACR) Category
Table 9: Association between Urine Dipstick Test Results and ACR of diabetic patient's participation in this study (n=110).
According to Table 9, dipstick testing showed limited sensitivity: 46.4%were negative or trace, yet 28 patients in this group had microalbuminuria on ACR testing. Only 3.6% of patients with macroalbuminuria were identified as>1+proteinuria on dipstick. This demonstrates the inadequacy of dipstick urinalysis alone for early nephropathy detection and highlights the superiority of quantitative ACR testing.
|
Dipstick Result |
<30 mg/g |
30-300 mg/g |
>300 mg/g |
Total |
|
Negative/Trace |
19 (17.3%) |
28 (25.5%) |
4 (3.6%) |
51 (46.4%) |
|
Trace to 1+ |
3 (2.7%) |
35 (31.8%) |
7 (6.4%) |
45 (40.9%) |
|
1+ or more |
0 (0.0%) |
3 (2.7%) |
8 (7.3%) |
11 (10.0%) |
|
Missing |
0 (0.0%) |
3 (2.7%) |
0 (0.0%) |
3 (2.7%) |
|
Total |
22 (20%) |
69 (62.7%) |
19 (17.3%) |
110 (100%) |
Table 9: Association between Urine Dipstick Test Results and Albumin-to-Creatinine Ratio (ACR) Category
Table 10: Association between Glycemic Control (HbA1c) and ACR of diabetic patient's participation in this study (n=110).
As presented in Table4.10, poor glycemic control (HbA1c>6.5%) was found in 71.8% of patients, and strongly associated with both microalbuminuria (44.5%) and macroalbuminuria (11.8%). In contrast, patients with prediabetes (5.7-6.4%) showed lower prevalence of albuminuria (6.4% microalbuminuria, 0.9 macroalbuminuria). This confirms hyperglycemia as a major risk factor for diabetic nephropathy.
|
HbA1c Category |
<30 mg/g |
30-300 mg/g |
>300 mg/g |
Total |
|
Prediabetes (5.7-6.4%) |
3 (2.7%) |
7 (6.4%) |
1 (0.9%) |
11 (10.0%) |
|
Diabetes (≥6.5%) |
17 (15.5%) |
49 (44.5%) |
13 (11.8%) |
79 (71.8%) |
|
Missing |
2 (1.8%) |
13 (11.8%) |
5 (4.5%) |
20 (18.2%) |
|
Total |
22 (20%) |
69 (62.7%) |
19 (17.3%) |
110 (100%) |
Table 10: Association between Glycemic Control (HbA1c) and Albumin-to-Creatinine Ratio (ACR) Category
Discussion
This study provides a critical analysis of the prevalence and risk factors for Diabetic Nephropathy (DN) in cohort of 110 diabetic patient, using the Albumin-to-Creatinine Ratio (ACR)as an early biomarker. The findings reveal patterns that are largely consistent with the global body of evidence, while also uncovering significant gaps in local clinical practice that warrant urgent attention.
Age, Diabetes Type, and Disease Burden
The study revealed that the highest proportion of participants were in the 41-50 and over 60 age groups, which aligns with the cumulative nature of diabetic complications. Type II diabetes accounted for 92.7% of the sample and was associated with a higher prevalence of micro- and macroalbuminuria. These findings are consistent with the International Diabetes Federation (IDF) data indicating that Type II diabetes is the primary driver of DN worldwide, due to its high prevalence and prolonged undiagnosed hyperglycemia [62,63].
Disease Duration and Glycemic Control
As expected, there was a strong correlation between diabetes duration and the risk of nephropathy. Patients with a disease duration exceeding 10 years had the highest rate of macroalbuminuria (9.1%). This confirms the natural progression from normoalbuminuria to microalbuminuria and then overt proteinuria, as documented in the UKPDS study. Moreover, poor glycemic control (HbA1c ≥ 6.5%) was a major risk factor, present in 71.8% of patients and strongly associated with albuminuria. These findings support the conclusions of the DCCT/EDIC studies, which demonstrated that intensive glycemic control significantly reduces the risk of developing nephropathy [64,65].
Hypertension as a Comorbid Factor
Although the prevalence of hypertension (30.9%) in this cohort was lower than in other studies, its presence was associated with a higher prevalence of microalbuminuria. These results emphasize the synergistic role of hypertension and hyperglycemia in causing kidney injury. Both contribute to intraglomerular hypertension and fibrosis, accelerating renal function decline. This is consistent with the findings of the RENAAL study, which demonstrated that intensive blood pressure control is as crucial as glycemic control in slowing DN progression [66].
Diagnostic Gap and Superiority of Quantitative Screening
A concerning finding was the large disparity between the biochemical prevalence of albuminuria (80% of patients had elevated ACR) and the formal clinical diagnosis of nephropathy (9.1%). This indicates a significant shortfall in routine screening and early diagnosis. These results reinforce international guidelines from ADA and KDIGO, emphasizing the use of quantitative ACR as a primary and effective screening tool rather than urine dipstick testing [67,68].
Silent Nature of Disease and Importance of Follow-Up
The results underscore the asymptomatic progression of early-stage DN, with 30% of patients reporting no symptoms despite abnormal ACR levels. This aligns with the known clinical course, where symptoms typically appear only in advanced stages. Furthermore, delayed healthcare visits (>1 year since last check-up) were associated with higher rates of macroalbuminuria, highlighting the critical importance of regular, protocol-driven follow-up regardless of symptom presence [65,69].
Treatment Patterns and Disease Severity
The association between insulin therapy (alone or combined) and more advanced stages of nephropathy likely reflects that these patients represent a subgroup with longer disease duration, beta-cell failure, or treatment-resistant hyperglycemia. This aligns with the understanding that insulin requirement in Type II diabetes often indicates advanced disease, which carries a higher risk of microvascular complications, including nephropathy.
Conclusion
This study reveals a high prevalence of diabetic nephropathy among diabetic patients attending Al-Wahda Hospitals in Dhamar, Yemen, with the majority of cases identified as microalbuminemia. Diabetic nephropathy was strongly associated with longer diabetes duration, poor glycemic control and hypertension. A significant diagnostic gap was observed, as most patients with biochemical evidence of nephropathy lacked a formal clinical diagnosis. Urine dipstick testing showed limited sensitivity for early detection compared with quantitative Albumin-to-creatinine Ratio (ACR). These findings indicate that diabetic nephropathy is common, largely and insufficiently screening in this sitting under-diagnosed.
Recommendations
Routine quantitative ACR screening should be integrated into standard diabetic care for early detection of nephropathy. Improved glycemic and blood pressure control, regular patient follow-up, and enhanced clinician awareness are essential to prevent disease progression. Further prospective studies are recommended to assess long-term renal outcomes and the impact of early intervention strategies.
References
- Blair, M. (2016). Diabetes mellitus review. Urologic Nursing, 36(1), 27-36.
- Egan, A. M., & Dinneen, S. F. (2019). What is diabetes? Medicine, 42, 679-681.
- Savitha, A. (2016). The need for patient follow-up strategies to confirm diabetes mellitus in large-scale opportunistic screening. Journal of Clinical and Diagnostic Research, 10(1), LE01-LE04.
- Lin, X., Xu, Y., Pan, X., Xu, J., Ding, Y., Sun, X., Song, X.,Ren, Y., & Shan, P. (2020). Global, regional, and national burden and trend of diabetes in 195 countries and territories: An analysis from 1990 to 2025. Scientific Reports, 10, 14790.
- Cho, N. H., Shaw, J. E., Karuranga, S., Huang, Y., da Rocha Fernandes, J. D., Ohlrogge, A. W., & Malanda, B. (2018). IDF diabetes atlas: Global estimates of diabetes prevalence for 2017 and projections for 2045. Diabetes Research and Clinical Practice, 138, 271-281.
- Centers for Disease Control and Prevention. (2022). National diabetes statistics report 2022
- Centers for Disease Control and Prevention. (2023). What is diabetes?
- World Health Organization. (2019). Classification of diabetes mellitus.
- Nomiyama, T., & Yanase, T. (2015). Secondary diabetes. Nihon Rinsho. Japanese Journal of Clinical Medicine, 73, 2008-2012.
- Repaske, D. R. (2016). Medication-induced diabetes mellitus.Pediatric Diabetes, 17, 392-397.
- Roep, B. O., Thomaidou, S., Van Tienhoven, R., & Zaldumbide, A. (2021). Type 1 diabetes mellitus as a disease of the β-cell (do not blame the immune system?). Nature Reviews Endocrinology, 17(3), 150-161.
- Galicia-Garcia, U., Benito-Vicente, A., Jebari, S., Larrea-Sebal, A., Siddiqi, H., Uribe, K. B., ... & Martín, C. (2020). Pathophysiology of type 2 diabetes mellitus. International journal of molecular sciences, 21(17), 6275.
- Katsarou, A., Gudbjörnsdottir, S., Rawshani, A., Dabelea, D., Bonifacio, E., Anderson, B. J., ... & Lernmark, Å. (2017). Type 1 diabetes mellitus. Nature reviews Disease primers, 3(1), 1-17.
- Waly, M. I., Essa, M. M., & Ali, A. (2010). The global burden of type 2 diabetes: a review. Int J Biol Med Res., 1(4), 326-329.
- Fowler, M. J. (2011). Microvascular and macrovascular complications of diabetes. Clinical Diabetes, 26, 77-82.
- Chawla, A., Chawla, R., & Jaggi, S. (2016). Microvascular and macrovascular complications in diabetes mellitus: Distinct or continuum? Indian Journal of Endocrinology and Metabolism, 20(4), 546-551.
- Harding, J. L., Pavkov, M. E., Magliano, D. J., Shaw, J. E., & Gregg, E. W. (2019). Global trends in diabetes complications: A review of current evidence. Diabetologia, 62(1), 3-16.
- Giglio, R. V., Patti, A. M., Rizvi, A. A., et al. (2023). Advances in the pharmacological management of diabetic nephropathy: A 2022 international update. Biomedicines, 11, 291.
- Thomas, M. C., Brownlee, M., Susztak, K., et al. (2015). Diabetic kidney disease. Nature Reviews Disease Primers, 1, 15018.
- Rossing, P., Persson, F., & Frimodt-Møller, M. (2018). Prognosis and treatment of diabetic nephropathy: Recent advances and perspectives. Nephrologie & Therapeutique, 14(Suppl 1), S31-S37.
- Hahr, A. J., & Molitch, M. E. (2015). Management of diabetes mellitus in patients with chronic kidney disease. Clinical Diabetes and Endocrinology, 1, 1-9.
- Abu-Farha, M., Iizuka, K., Yabe, D., Al-Mulla, F., & Abubaker,J. (2023). Advances in the research of diabetic nephropathy.Frontiers in Endocrinology, 13, 1116188.
- Dronavalli, S., Duka, I., & Bakris, G. L. (2008). The pathogenesis of diabetic nephropathy. Nature Clinical Practice Endocrinology & Metabolism, 4(8), 444-452.
- Jiang, W., Wang, J., Shen, X., et al. (2020). Establishment and validation of a risk prediction model for early diabetic kidney disease based on a systematic review and meta-analysis of 20 cohorts. Diabetes Care, 43, 925-933.
- Papadopoulou-Marketou, N., Paschou, S. A., Marketos, N., Adamidi, S., Adamidis, S., & Kanaka-Gantenbein, C. (2018). Diabetic nephropathy in type 1 diabetes. Minerva Medica, 109, 218-228.
- Lim, A. K. H. (2014). Diabetic nephropathy—Complications and treatment. International Journal of Nephrology and Renovascular Disease, 7, 361-381.
- Satirapoj, B., & Adler, S. G. (2015). Prevalence and management of diabetic nephropathy in western countries. Kidney Diseases, 1(1), 61-70.
- Liyanage, T., Toyama, T., Hockham, C., et al. (2022). Prevalence of chronic kidney disease in Asia: A systematic review and analysis. BMJ Global Health, 7, e007525.
- Badro, D. A. (2023). Chronic kidney disease management in developing countries. In Y. M. Al-Worafi (Ed.), Handbook of medical and health sciences in developing countries: Education, practice, and research (pp. 1-146). Springer, Cham.
- Saeedi, P., Petersohn, I., Salpea, P., et al. (2019). Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas (9th ed.). Diabetes Research and Clinical Practice, 157, 107843.
- Gregg, E. W., Sattar, N., & Ali, M. K. (2016). The changing face of diabetes complications. The Lancet Diabetes & Endocrinology, 4(6), 537-547.
- Thomas, M. C., Brownlee, M., Susztak, K., et al. (2015). Diabetic kidney disease. Nature Reviews Disease Primers, 1, 15018.
- Alicic, R. Z., Rooney, M. T., & Tuttle, K. R. (2017). Diabetic kidney disease: Challenges, progress, and possibilities. Clinical Journal of the American Society of Nephrology, 12(12), 2032-2045.
- Basile, J. N., & Bloch, M. J. (2020). The progression of diabetic nephropathy and its risk factors. Clinical Diabetes, 38(3), 238-246.
- Zhang, L., Long, J., Jiang, W., et al. (2022). Trends in chronic kidney disease in China. The New England Journal of Medicine, 387(15), 1438-1440.
- Nicholas, S. B., Kalantar-Zadeh, K., & Norris, K. C. (2015). Socioeconomic disparities in chronic kidney disease. Advances in Chronic Kidney Disease, 22(1), 6-15.
- Crews, D. C., Liu, Y., & Boulware, L. E. (2014). Disparities in the burden, outcomes, and care of chronic kidney disease. Current Opinion in Nephrology and Hypertension, 23(3), 298-305.
- Fenta, E. T., Yismaw, M. B., & Gesesew, H. A. (2023). Prevalence and predictors of chronic kidney disease among patients with type 2 diabetes mellitus in Africa: A systematic review and meta-analysis. Diabetology & Metabolic Syndrome, 15, 114.
- Kaze, A. D., Ilori, T., Jaar, B. G., & Echouffo-Tcheugui, J.B. (2021). Burden of chronic kidney disease on the African continent: A systematic review and meta-analysis. BMC Nephrology, 22(1), 1-12.
- Goldin, A., Beckman, J. A., Schmidt, A. M., & Creager, M.A. (2006). Advanced glycation end products: Sparking the development of diabetic vascular injury. Circulation, 114(6), 597-605.
- Brownlee, M. (2001). Biochemistry and molecular cell biology of diabetic complications. Nature, 414(6865), 813-820.
- Ganz, M. B., & Saksa, B. (2009). Protein kinase C in the diabetic kidney. Kidney International, 75(Suppl 106), S67-S72.
- Jha, J. C., Banal, C., Chow, B. S., Cooper, M. E., & Jandeleit-Dahm, K. (2016). Diabetes and kidney disease: Role of oxidative stress. Antioxidants & Redox Signaling, 25(12), 657-684.
- Magee, G. M., Bilous, R. W., Cardwell, C. R., et al. (2009). Is hyperfiltration associated with the future risk of developing diabetic nephropathy? A meta-analysis. Diabetologia, 52(4), 691-697.
- Brenner, B. M., Cooper, M. E., de Zeeuw, D., et al. (2001). Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy. The New England Journal of Medicine, 345(12), 861-869.
- Reidy, K., Kang, H. M., Hostetter, T., & Susztak, K. (2014). Molecular mechanisms of diabetic kidney disease. Journal of Clinical Investigation, 124(6), 2333-2340.
- Meng, X. M., Nikolic-Paterson, D. J., & Lan, H. Y. (2016). TGF-β: The master regulator of fibrosis. Nature Reviews Nephrology, 12(6), 325-338.
- American Diabetes Association. (2024). Chronic kidney disease and risk management: Standards of medical care in diabetes—2024. Diabetes Care, 47(Suppl. 1), S164-S179.
- Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. (2013). KDIGO 2012 clinical practice guideline for the evaluation and management of chronic kidney disease. Kidney International Supplements, 3(1), 1-150.
- The Diabetes Control and Complications Trial (DCCT) Research Group. (1993). The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. The New England Journal of Medicine, 329(14), 977-986.
- UK Prospective Diabetes Study (UKPDS) Group. (1998). Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). The Lancet, 352(9131), 837-853.
- Whelton, P. K., Carey, R. M., Aronow, W. S., Casey, D. E., Collins, K. J., Dennison Himmelfarb, C., ... & Wright, J. T. (2018). 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA guideline for the prevention, detection, evaluation, and management of high blood pressure in adults. Journal of the American College of Cardiology, 71(19), e127-e248.
- Lewis, E. J., Hunsicker, L. G., Clarke, W. R., Berl, T., Pohl,M. A., Lewis, J. B., ... & Rohde, R. D. (2001). Renoprotective effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy due to type 2 diabetes. New England Journal of Medicine, 345(12), 851-860.
- Brenner, B. M., Cooper, M. E., De Zeeuw, D., Keane, W. F., Mitch, W. E., Parving, H. H., ... & Shahinfar, S. (2001). Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy. New England Journal of Medicine, 345(12), 861-869.
- Zinman, B., Wanner, C., Lachin, J. M., Fitchett, D., Bluhmki, E., Hantel, S., ... & Inzucchi, S. E. (2015). Empagliflozin, cardiovascular outcomes, and mortality in type 2 diabetes. New England Journal of Medicine, 373(22), 2117-2128.
- Perkovic, V., Jardine, M. J., Neal, B., Bompoint, S., Heerspink, H. J. L., Charytan, D. M., ... & Mahaffey, K. W. (2019). Canagliflozin and renal outcomes in type 2 diabetes and nephropathy. New England Journal of Medicine, 380(24), 2295-2306.
- Bakris, G. L., Agarwal, R., Anker, S. D., Pitt, B., Ruilope, L. M., Rossing, P., ... & Filippatos, G. (2020). Effect of finerenone on chronic kidney disease outcomes in type 2 diabetes. New England Journal of Medicine, 383(23), 2219-2229.
- Orth, S. R., & Hallan, S. I. (2008). Smoking: A risk factor for progression of chronic kidney disease and for cardiovascular morbidity and mortality in renal patients—absence of evidence or evidence of absence? Clinical Journal of the American Society of Nephrology, 3(1), 226-236.
- Eknoyan, G., Lameire, N., Eckardt, K. U., Kasiske, B. L.,Wheeler, D. C., Levin, A., ... & Cheung, M. (2013). KDIGO clinical practice guideline for the management of blood pressure in chronic kidney disease. Kidney International Supplements, 3(5), 337-414.
- Tuttle, K. R., Agarwal, R., Alpers, C. E., Bakris, G. L.,Brosius, F. C., Coca, S. G., ... & Heerspink, H. J. L. (2022). Molecular mechanisms and therapeutic targets for diabetic kidney disease. Kidney International, 102(2), 248-260.
- Martinez Leon, V., Hilburg, R., & Susztak, K. (2024). Mechanisms of diabetic kidney disease and established and emerging treatments. Nature Reviews Endocrinology, 20(5), 265-278.
- Zhang, L., Jiang, L., Xu, R., Zhang, X., Zhang, B., & Yue,R. (2025). Epidemiological research on diabetic nephropathy at global, regional, and national levels from 1990 to 2021: an analysis derived from the global burden of disease 2021 study. Frontiers in Endocrinology, 16, 1647064.
- Christofides, E. A., & Desai, N. (2021). Optimal early diagnosis and monitoring of diabetic kidney disease in type 2 diabetes mellitus: addressing the barriers to albuminuria testing. Journal of primary care & community health, 12, 21501327211003683.
- Gheith, O., Farouk, N., Nampoory, N., Halim, M. A., & Al-Otaibi, T. (2015). Diabetic kidney disease: world wide difference of prevalence and risk factors. Journal of nephropharmacology, 5(1), 49.
- Hussain, S., Jamali, M. C., Habib, A., Hussain, M. S., Akhtar, M., & Najmi, A. K. (2021). Diabetic kidney disease: An overview of prevalence, risk factors, and biomarkers. Clinical Epidemiology and Global Health, 9, 2-6.
- McGrath, K., & Edi, R. (2019). Diabetic kidney disease: diagnosis, treatment, and prevention. American family physician, 99(12), 751-759.
- Zahra, S., Saleem, M. K., Ejaz, K. F., Akbar, A., Jadoon, S. K., Hussain, S., ... & Alvi, S. (2024). Prevalence of nephropathy among diabetic patients in North American region: a systematic review and meta-analysis. Medicine, 103(38), e39759.
- Shin, J. I., Chang, A. R., Grams, M. E., Coresh, J., Ballew,S. H., Surapaneni, A., ... & Gansevoort, R. T. (2021). Albuminuria testing in hypertension and diabetes: an individual-participant data meta-analysis in a global consortium. Hypertension, 78(4), 1042-1052.
- Xie, D., Ma, T., Cui, H., Li, J., Zhang, A., Sheng, Z., & Xie,Y. (2023). Global burden and influencing factors of chronic kidney disease due to type 2 diabetes in adults aged 20-59 years, 1990-2019. Scientific reports, 13(1), 20234.
- Hoogeveen, E. K. (2022). The epidemiology of diabetic kidney disease. Kidney and Dialysis, 2(3), 433-442.
