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    2010 Societ Italiana di Nefrologia - ISSN 1121-8428

    JN (2010; :05) 547-55523EPHROL

    INTRODUCTION

    Systemic hypertension is a major health problem world-

    wide and Blacks are more prone to its complications (1,

    2). About 4.33 million Nigerians aged 15 years and above,

    corresponding to 9.3% of the population, are hypertensive

    based on a systolic blood pressure of 160 mmHg and a

    diastolic pressure of 90 mmHg (3, 4). However, when the

    World Health OrganizationInternational Society of Hyper-

    tension (WHO/ISH) guidelines of 1999 were applied to the

    above data, the estimated prevalence of hypertension was

    17% to 20% or more (5, 6). Although the prevalence rate is

    lower than the figure reported for the United States (>25%)

    (7), the mortality associated with the disease in Nigeria has

    been observed to be higher (8). Hypertension has a cause

    and effect relationship with kidney disease and is a major

    factor responsible for progression to End-Stage Renal Dis-

    ease (ESRD) (9-12). The risk factors that have been found

    to predispose hypertensive to developing ESRD include:

    Black race, positive family history, long-standing or severe

    hypertension, age of onset of hypertension between 25 and

    45 years old, presence of hypertensive retinopathy, and left

    ventricular hypertrophy (13). Many studies in Nigeria have

    shown that hypertension and chronic glomerulonephritis

    topped the list of common causes of chronic renal failure

    (CRF) (14-16). In a prospective study of 1,980 patients,

    Ojogwu (16)observed that the most common cause (43%

    of cases) of chronic renal failure was hypertensive nephro-

    sclerosis. This was followed by obstructive uropathy (33%)

    and chronic glomerulonephritis (18%). He observed that

    the frequency and severity of hypertension in Nigerians and

    their propensity to develop renal failure are similar to what

    obtains in American Blacks. Similarly, Akinsola et al (17)

    reported that hypertension was second to chronic glom-

    erulonephritis as a cause of chronic renal failure, the care

    of which is unaffordable to the majority of patients. This

    underscores the need to emphasize strategies for prevent-

    ing the development of progressive renal disease with early

    recognition of clinical markers of chronic kidney disease

    ABSTRACT

    Background: Urinary sediment examination and dip-

    stick urinalysis are an integral part in evaluating hy-

    pertensive patients. This study aims to determine theprevalence of urinary sediment abnormalities and

    compare this result with dipstick urinalysis in hyper-

    tensive Nigerians.

    Methods: 138 newly diagnosed, adult, hypertensive

    Nigerians were studied. They were compared with

    an age- and sex-matched non-hypertensive control

    group from the general population. The subjects urine

    samples were analyzed by dipstick test and micros-

    copy (bright field), enhanced by Sternheimers stain.

    Significant sediments were defined as 3/hpf and dip-

    stick proteinuria or hematuria as 1+.

    Results: Mean age was 43.219.64 yrs and 43.199.55

    yrs in patients and controls respectively with 76 (55%)males in the patients and 80 (58%) in controls. Micro-

    scopic hematuria (3/hpf) was detected in 15.2% of

    the patients and 3.6% of the control group (p=0.0009).

    Other elements present in insignificant quantities

    in patients and controls, respectively, were: leuko-

    cytes (7.2%, 9.4%, p=0.513); hyaline casts (5.8%,

    8%, p=0.476), granular casts (1.4%, 0%) and crystals

    (6.5%, 5.1%, p=0.606). Dipstick proteinuria with he-

    maturia was found in 6.55% and proteinuria alone in

    1.45% of cases, while the control group showed 2.2%

    and 1.45% of hematuria and proteinuria, respectively;

    47.6% of hypertensive patients with urinary sediment

    hematuria were not detected by dipstick test.Conclusions: Hypertensive Nigerians showed a high

    prevalence of microscopic hematuria which may be

    suggestive of sub-clinical kidney damage at diagno-

    sis. There is a high false-negative rate with dipstick

    urinalysis, underscoring the need for routine examina-

    tion of urinary sediment in the assessment of hyper-

    tensive patients.

    Key words: Dipstick tests, Hypertension, Nigerians,

    Urinary sediments

    Division of Nephrology, Department of Medicine,

    University of Ilorin Teaching Hospital, Ilorin - Nigeria

    Division ofNephrology, DepartmentofMedicine, University ofIlorin TeachingHospital, Ilorin -Nigeria

    Timothy O. Olanrewaju, Ademola Aderibigbe

    Pattern of urinary sediments and comparison

    with dipstick urinalysis in hypertensive Nigerians

    ORIGINAL ARTICLE

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    Olanrewaju and Aderibigbe: Urinary sediment evaluation in hypertension

    (18). In a developing nation like Nigeria, such strategies

    involve a simple urine test to detect early renal damage.

    Early detection of patients with glomerulonephritis will at-

    tract appropriate intervention measures to prevent or delay

    progression to ESRD.

    There are many markers for assessing renal damage.

    These range from very sensitive endogenous markers such

    as cystatin C, microalbuminuria and proteinuria to serum

    urea, creatinine, uric acid, creatinine clearance and uri-

    nary sediment. While some of these markers are indeed

    sensitive, they can be expensive as a screening tool for

    early detection of renal damage. The examination of uri-

    nary sediments under the microscope for abnormalities is

    a recognized method for assessing renal damage irrespec-

    tive of the cause,and some characteristic features of the

    sediment have been used to determine the type and pos-

    sibly the severity of renal disease (19). The findings in the

    sediment of red blood cells or red blood cell casts, white

    blood cells or white blood cell casts, oval fat bodies or fatty

    casts and broad casts are almost diagnostic of glomeru-

    lonephritis, pyelonephritis, nephritic syndrome and renal

    failure, respectively (19). Thus, urinary sediment analysis

    tends to give information about the etiology of renal dis-

    eases, helps in prognostication, and may offer a simpler

    index for evaluating the stage of renal damage in patients

    with newly diagnosed hypertension. The facilities are read-

    ily available, the samples can be collected anywhere and

    its collection is noninvasive. Urinary sediment examination

    has therefore been recommended for evaluation of hyper-

    tension in order to determine the cause and/or effect rela-

    tionship (5, 20, 21).

    Though some studies have been done on urinary abnormali-

    ties in Nigeria, most of them were carried out on children and

    adolescents using dipstick urinalysis (22-26). There is pau-

    city of published studies on urinary sediments among Nige-

    rians and in particular, adult hypertensive patients. Hence

    this study was designed to evaluate the pattern of urinary

    sediments and compare the results with dipstick urinalysis

    in newly diagnosed, adult Nigerian hypertensive patients.

    MATERIALSANDMETHODS

    Study design and location

    This was a cross-sectional study of consecutively recruit-

    ed, consenting patients. The study was carried out at the

    General Out-patient Department (GOPD), Medical Outpa-

    tient Department (MOPD), Accident and Emergency (A/E)

    Department of the University of Ilorin Teaching Hospital

    (UITH) and the Federal Staff Clinic at the Federal Secre-

    tariat in Ilorin. Ilorin is the capital city of Kwara State, which

    is one of the states in the north-central zone of Nigeria.

    UITH Ilorin serves both Kwara State as well as five other

    adjoining states.

    Selection of subjects

    The inclusion criteria for patients were newly diagnosed,

    adult hypertensive patients aged 18 years and above with

    average systolic blood pressure of 140 mmHg and/or a

    diastolic pressure of 90 mmHg who were not on drugs

    and who consented to the study by filling in the consent

    form. The exclusion criteria included (i) patients with dia-

    betic mellitus, sickle cell disease, history of/or established

    renal disease, malignancy and clinical evidence of connec-

    tive tissue disease; (ii) women who are pregnant, in peupe-

    rium or those menstruating; (iii) patients who are on anti-

    hypertensive drugs; and (iv) those who have just completed

    rigorous exercise or are on any medications. For the control

    group, the inclusion criteria were healthy, non-hypertensive,

    age- and sex-matched individuals who have not undergone

    rigorous exercise; and the exclusion criteria included indi-

    viduals with high blood pressure and those that fulfilled the

    exclusion criteria as stated for the subject group.

    Ethical clearance

    An approval was obtained from the ethical and research

    committee of the University of Ilorin Teaching Hospital be-

    fore commencing the study. All patients and controls who

    participated in the study signed the informed consent be-

    fore recruitment.

    Evaluation and investigation protocols

    Clinical

    Detailed biodata and socio-demographic parameters were

    obtained from the patients and controls using structured

    questionnaires. Weight (WT) was measured using the por-

    table SECA weighing scale placed on a flat, hard surface

    with the subjects wearing light clothing and height mea-

    sured with subjects standing without shoes. Body mass in-

    dex was calculated from height and weight. Blood pressure

    was measured in sitting position with a mercury sphygmo-

    manometer with standard cuff (25 cm x 12 cm) on the right

    arm after 5 minutes of rest. Korotkoff phases I and V were

    taken as systolic blood pressure (SBP) and diastolic blood

    pressure (DBP), respectively. Hypertension was defined

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    based on the Seventh Report of the Joint National Commit-

    tee on Prevention, Detection, Evaluation and Treatment of

    High Blood Pressure (JNC VII) (1). Two measurements were

    taken at least 5 minutes apart and the value of the mean

    was used for the study. The mean arterial pressure (MAP)

    and pulse pressure (PP) were also determined.

    Serum biochemistry and urineculture

    Blood samples for urea and creatinine were collected in

    heparinized bottles and analyzed at the Chemical Pathol-

    ogy Laboratory of the hospital using an RA-50 spectro-

    photometer (Bayer, Germany). Urea (Ur) was analyzed by

    diacetyl monoxime method while Jaffes reaction was used

    for creatinine (Cr). Also, fasting plasma glucose (FPG) sam-

    ples were collected in a fluoride oxalate bottle and ana-

    lyzed at the same laboratory by glucose oxidase method.

    Urine culture was done to exclude urinary tract infections.

    Glomerular filtration rate (GFR) was estimated by the Cock-

    roft and Gault formula which has been validated in Nigerian

    patients (27).

    Dipstick urinalysis

    About 10 mL of early morning, clean catch urine was col-

    lected in a sterile test tube. The urine was examined physi-

    cally and tested with urinanalysis reagent strips (Multistix

    10 SG; Bayer, Leverkusen, Germany). Each parameter

    tested (e.g., protein, blood, leukocytes, and nitrite) was read

    manually within the specified time limit as indicated by the

    manufacturer of the dipsticks. Protein 1 + and blood more

    than trace were considered to be significant.

    Urine sediment microscopy

    This procedure was carried out in the renal laboratory by the

    investigator with the assistance of an experienced laborato-

    ry technologist. A standard urinary sediment Atlas produced

    by Fogazzi et al (19) was used for clarification as deemed

    necessary. A 10 mL early morning, first void, clean catch

    urine was collected in a sterile tube and centrifuged for 5

    minutes at 2000 rpm. The supernatant was decanted leav-

    ing approximately 0.5 mL volume of the sediment. In order

    to enhance the identification of the constituent elements

    of the sediment, Sternheimers stain was applied. Stern-

    heimers stain is one of the most popular supravital stains

    which, in the absence of a phase contrast microscope,

    helps to partly overcome the limitations of the bright field

    microscope (28). It is a mixture of Copper-phthalocyanine

    dye, national fast blue and a xanthene dye called pyronin

    B. A drop of this stain was added to the 0.5 mL sediment

    and left for 10 minutes to allow the staining to develop and

    increase in intensity. This enhances a good differentiation of

    red blood cells, white blood cells, epithelial cells, and casts.

    The stained urine sediment was resuspended by gentle agi-

    tation and a drop was pipetted using a micropipette onto a

    clean glass slide and covered with a clean cover-slip. The

    sediment was then examined under the bright-field micro-

    scope, first under low (x 100 magnifications) and then high

    power (x 400 magnifications). Ten to fifteen fields were ex-

    amined in the low and high power objectives. Each of the

    constituent elements of the sediment was recorded as an

    average number per high power field (hpf). The presence of

    sediment cells >2/hpf and casts or crystals as indicated by

    a plus (+) were considered significant.

    Data analysis

    The data were analyzed by SPSS version 12.0.1 (SPSS Inc.,

    Chicago, IL, USA). Means and standard deviations were

    used to summarize numerical/quantitative variables. The

    statistical significance of differences in patients and con-

    trol groups was estimated using chi-square for categorical

    variables and Students t-test for continuous variables. The

    proportion of patients with abnormal urinary sediment was

    determined. The level of statistical significance was taken

    as a p value of < 0.05.

    RESULTS

    The demographic, clinical and laboratory characteristics

    of the patients and control subjects are shown in Table

    I. There was no difference between the mean age of the

    patients and the control subjects, showing that they were

    well matched. There was also no difference in the fasting

    plasma glucose between the two groups. However, the pa-

    tient group had significantly higher values of weight, BMI,

    SBP, DBP, MAP and PP than control subjects (p2/hpf) with a range of

    3-10/hpf. In the control group, 119 (86.2%) had no RBC,

    14 (10.2%) had 1-2/hpf and only 5 (3.6%) had > 2/hpf of

    RBCs in the urinary sediment (Fig. 1). The difference in the

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    microscopic hematuria between the patients (15.2%) and

    controls (3.6%) was significant (p=0.001).White blood cells

    (WBC) of 1-2/hpf were detected in 10 (7.2%) of the pa-

    tients while the remaining 128 (92.8%) had no WBC. In the

    control group, 13 (9.4%) had 1-2/hpf of WBC while 125

    (90.6%) had no WBC (Fig. 2). Granular casts of 1-2/hpf

    Fig. 1 - Urinary sediment red blood cells per high power field(hpf) in study subjects. White columns = patient; black col-umns = control.

    Fig. 2 - Urinary sediment white blood cells per high powerfield (hpf) in study subjects. White columns = patient; blackcolumns = control.

    TABLE I

    CLINICAL AND LABORATORY CHARACTERISTICS OF THE SUBJECTS

    Characteristics Patients Control p value

    Age (years) 43.21 9.64 43.19 9.55 0.9862

    Gender: male, n (%) 76 (55) 80 (58)

    Weight (Kg) 72.63 14.29 69.34 12.55 0.0431

    Body Mass Index (kg/m2) 26.18 5.12 23.34 9.02 0.0015

    Systolic Blood Pressure (mmHg) 154.32 17.2 119.44 11.94 < 0.001

    Diastolic Blood Pressure (mmHg) 98.67 16.87 76.11 6.14 < 0.001

    Pulse Pressure (mmHg) 59.64 19.79 43.33 11.32 < 0.001

    Mean Arterial Pressure (mmHg) 114 14.21 90.55 6.65 < 0.001

    Urea (mmol/L) 5.27 1.39 4.86 1.24 0.0102

    Creatinine (umol/L) 76.06 22.49 67.55 15.9 0.0003

    Fasting plasma glucose (mmol/L) 4.12 1.23 96 1.29 0.2926

    Glomerular filtration rate (ml/min/1.73m2) 107.6 0 52.85 122.17 44.3 0.0134

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    were present in only 2 (1.4%) of the patients and none in the

    control subjects, while hyaline casts of 1-2/hpf were found

    in 8 (5.8%) patients and 11 (8%) control subjects (Tab. II).

    Crystals were detected in 9 patients (6.5%) and 7 (5.1%)

    of the control subjects (Tab. II). RBC cast, WBC cast, waxy

    and broad casts were not found in either patients or control

    subjects. Significant proteinuria (1+) was found in 11 (8%)

    of the patients with 8 (5.8%) and 3 (2.2%) of them having

    1+ and 2+, respectively (Tab. III). In the control group, only

    2 (1.45%) had significant proteinuria. Significant hematuria

    1+) was present in 9 (6.5%) of the patients with 7 (5.1%)

    and 2 (1.45%) of them having 1+ and 2+, respectively, while

    only 3 (2.2%) of the controls had significant hematuria. Ta-

    ble IV shows the proportion of subjects with significant dip-

    stick findings as compared with microscopic findings. All

    the 9 patients with dipstick hematuria had proteinuria and

    all the 11 patients with dipstick proteinuria had significant

    microscopic hematuria. Ten patients out of the twenty-one

    (47.6%) that had significant microscopic hematuria were

    not detected by dipstick urinalysis. Similarly, the 2 controls

    that had significant proteinuria also had hematuria and the

    3 controls that had hematuria also had microscopic hema-

    turia. Two control subjects who had significant microscopic

    hematuria were not detected by dipstick urinalysis.

    TABLE II

    URINARY SEDIMENT CASTS AND CRYSTALS AMONG PATIENTS AND CONTROLS

    Parameters (per hpf) Patients Controls P value

    n (%) n (%)

    Hyaline cast: Nil 130 (94.2) 127 (92) 0.4757

    1-2 8 (5.8) 11 (8) 0.4757

    > 2 - - -

    Granular cast: Nil 136 (98.6) 138 (100) -

    1-2 2 (1.4) - -

    > 2 - - -

    Crystals Nil 129 (93.5) 131 (94.9) 0.6064

    1-2 9 (6.5) 7 (5.1) 0.6064 > 2 - - -

    Red blood cell and White blood cell casts were nil.

    hpf = high power field.

    TABLE III

    DIPSTICK URINALYSIS FINDINGS IN PATIENTS AND CONTROLS

    Patients Controls P value

    n (%) n (%)

    Protein Nil 127 (92) 13 (98.65) 0.0106

    1+ 8 (5.8) 2 (1.45) 0.0106

    2+ 3 (2.2) - -

    3+ - - -

    Blood Nil 129 (93.5) 135 (97.8) 0.0766

    1+ 7 (5.10) 3 (2.2) 0.0766

    2+ 2 (1.45) - -

    3+ - - -

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    DISCUSSION

    The pattern of urinary sediment in newly diagnosed,

    adult Nigerian hypertensive patients was found to be mi-

    croscopic hematuria in 34.8%, out of which 15.2% was

    significant in spite of moderately elevated blood pres-

    sure; leukocyturia in 7.2%, of which none was present in

    significant quantity (Figs. 1 and 2). Other findings were

    granular casts in 1.4%, hyaline casts in 5.8% and crystals

    in 6.5% of patients, all of which were present in normal

    quantities (Tab. II). When these parameters were com-

    pared with the control group, only the microscopic he-

    maturia showed a statistically significant difference. This

    suggests that the urinary sediment manifestation of early

    hypertensive renal damage is microscopic hematuria. In a

    similar study by Ratto et al (29), the prevalence of urinary

    sediment alterations in their patient population at baseline

    was 12.2% (leukocyturia 6.6% and microhematuria with

    or without leukocyturia 5.6%). The prevalence of micro-

    hematuria of 15.2% in our patients is significantly higher

    than the approximately 5.6% obtained in their study. This

    wide difference may be related to the racial difference of

    the study populations. While our study was conducted in

    a predominantly Black population, the study by Ratto et al

    was carried out among Caucasians. Blacks are known to

    have a high prevalence of hypertensive renal damage and

    they experience more rapid progression to ESRD. For ex-

    ample, the gender- and age-adjusted incidence of ESRD

    due to hypertension in Blacks is 8 times the rate among

    the Caucasians (30). Furthermore, it has been shown that

    hypertension at any level exacts a greater degree of car-

    diovascular and renal damage in Blacks than Whites and

    these target- organ complications occur much earlier in

    life among Blacks (31). The Ratto et al study found that

    the microhematuria in some of their patients was due to

    TABLE IV

    PROPORTION OF SUBJECTS WITH SIGNIFICANT DIPSTICK FINDINGS AND MICROSCOPIC HEMATURIA

    Patients Controls p value

    n (%) n (%)

    Dipstick proteinuria 11 (8) 2 (1.45) 0.0106

    Dipstick hematuria 9 (6.5) 3 (2.2) 0.7656

    Microscopic hematuria 21 (15.2) 5 (3.6) 0.0010

    renal diseases such as nephrosclerosis, interstitial dis-

    ease, glomerulonephritis, etc. but the relative proportion

    of these underlying diseases was not documented. The

    prevalence of leukocyturia of 7.2% in our patients is com-

    parable to the findings of Ratto et al (6.6%). Also impor-

    tant is the fact that the leukocyturia in our patients was

    present in an insignificant quantity and so it is difficult to

    ascribe it to an underlying renal disease, although Ratto

    et al ascribed leukocyturia in some of their female patients

    to urinary tract infection. Granular casts and crystals were

    present more in the study subjects while hyaline casts

    were more present in the control group. However, the dif-

    ference was not statistically significant, hence, possible

    primary glomerular disease could not be ascribed to the

    elevated blood pressure in the study subjects. The pres-

    ence of granular casts is suspicious in the 2 patients in

    whom they were found, although they were present in

    normal quantities. A follow-up of these patients will be

    necessary to determine their relevance in the long term,

    since although casts and crystals were not analyzed by

    Ratto et al, their study showed an increased prevalence

    of microhematuria (5.6% to 7.4%) and leukocyturia (6.6%

    to 17%) after a 6.6-year follow-up of their patients. Red

    blood cell, white blood cell and epithelial cell casts were

    not detected in our patients or the control subjects. This is

    not so surprising, because they are almost always present

    in active renal disease in most cases such as proliferate or

    acute glomerulonephritis, urinary tract infections or acute

    renal tubular disease which had already been excluded in

    our patient population as confounding factors.

    The prevalence of abnormal urinary sediment in newly di-

    agnosed hypertensive Nigerians was therefore found to be

    15.2%, essentially consisting of microhematuria. This fig-

    ure is substantially higher than the 3.6% found among the

    normotensive controls. Although the authors are not aware

    of any similar studies previously carried out in this group

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    of patients in our environment to compare this prevalence

    rate, this value is rather high. The high prevalence rate

    shows that a significant number of Nigerian hypertensive

    patients already have subtle renal damage at the point of

    diagnosis, even though the other markers of renal dam-

    age such as serum creatinine and urea may still be within

    the normal limits. Moreover, a more sensitive marker of hy-

    pertensive renal damage such as microalbuminuria would

    probably detect a much higher number of these patients

    if this test was used. Indeed Olatunde et al (32) found the

    prevalence of microalbuminuria in their hypertensive pa-

    tients to be 17.4% despite the fact that 70% of the patients

    were already on antihypertensive drugs. The prevalence of

    microhematuria and microalbuminuria in hypertensive pa-

    tients are comparable perhaps because the mechanisms

    of their formation are almost similar, involving injury to the

    glomerular endothelium, although microhematuria requires

    greater and more intense injury and structural alterations.

    Routine screening of newly diagnosed hypertensive pa-

    tients for microalbuminuria would be rather costly for the

    majority of our patients in the developing world who are

    poor. The ISH-WHO of 1999 and the JNC guidelines for

    the management of hypertension have advocated routine

    urinalysis (both dipstick and microscopy) in the initial eval-

    uation of hypertensive patients so that renal damage can

    be detected early. The findings in this study suggest that

    a urinary microscopic could be a valuable screening tool

    not only for hypertensive renal damage but for renal condi-

    tions that have potential for renal vascular injury. Dipstick

    proteinuria was detected in 8% of the patients and 1.45%

    of controls. Although the prevalence rate among patients

    in this study was rather lower than the figure obtained by

    Kannel et al (18%) (33), Bulpitt et al (16%) (34)and Ljung-

    man et al (17%) (35), it is comparable to the findings of

    Wollf et al (10%) (36) and Samuelsson et al (6%) (37) but

    higher than the report by Lewin et al (4%) (38). A recent

    general population screening to detect renal disease in

    Germany reported a prevalence of persistent proteinuria of

    12% (104 of 856 participants with self-reported dipstick-

    positive proteinuria were confirmed by family physicians)

    and 45% of these have essential hypertension (39). The

    much higher prevalence observed in this study compared

    to ours may be due to differences in the study methodolo-

    gy and sensitivity of the test strips used to detect proteinu-

    ria. The majority of previous studies on dipstick proteinuria

    in Nigeria were done mainly on children and adolescents

    (22-26).While Ajasin (23) found the prevalence of isolated

    proteinuria among primary school children to be 8.6%,

    Akinkugbe FM et al (24) and Asani et al (26) obtained prev-

    alences of 5.4% and 1.95%, respectively, using similar cri-

    teria. Among the adolescents, Akinkugbe (22)reported a

    prevalence of 3.2% while Oviasu (25) obtained 4.7% with

    similar age ranges of 12 to 22 years and 13 to 20 years,

    respectively. These studies showed that the prevalence

    of proteinuria among the young age groups varies signifi-

    cantly, probably influenced by the geographical location.

    However, there seems to be a reduced prevalence among

    the older children. This observation cannot be applied to

    adulthood, in which there is higher predisposition to re-

    nal damage from various conditions such as hypertension.

    Dipstick hematuria was found in 9 (6.5%) patients and in

    only 3 (2.2%) of the control group in this study but the

    difference is not statistically significant (p=0.0766). In his

    study on adolescent students, Oviasu found a prevalence

    of 0.55%. It is however difficult to compare these groups

    because of the difference in the population characteris-

    tics. All the patients and controls with dipstick hematuria

    had proteinuria. The 21 (15.2%) patients that had micro-

    scopic hematuria were inclusive of the 11 (8%) that had

    dipstick proteinuria. This implies that about 47.6% of pa-

    tients with abnormal urinary sediment were not detected

    by the dipstick method. Similarly, 2 out of the 5 controls

    with microscopic hematuria were not picked out by the

    dipstick test. This high false- negative rate with dipstick

    urinalysis is higher than the 6.5% to 36% obtained in the

    literature (40-43). The difference might be due to the char-

    acteristics of the population of the patients studied. While

    this study focused on hypertensive patients, the majority

    of the other study populations were unselected cohorts.

    These high false- negative rates show that the sensitivity

    of dipstick test in detecting microscopic hematuria in adult

    hypertensive patients is poor.There has been a protract-

    ed debate on the usefulness of urinary microscopy com-

    pared with dipstick urinalysis in screening for diagnosis

    of asymptomatic disease. While some authors are of the

    opinion that microscopic examination of urinary sediment

    should be limited to those patients with abnormalities in

    the dipstick test, others strongly recommend its use as an

    initial evaluation of patients to forestall the high false-pos-

    itive and false-negative rates associated with the dipstick

    method which have been discussed earlier. Our findings

    in this study support the opinion that microscopy of the

    urine should be part of the initial evaluation of not only

    systemic hypertension but also other patients at a high risk

    for kidney damage. There was a significantly lower value

    of GFR in the patients than in the control subjects, which

    is in agreement with the higher serum creatinine in these

    patients. This suggests that renal function in hypertensive

    patients is depressed compared with normotensive con-

    trols. In conclusion, significant proportions of newly di-

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    Olanrewaju and Aderibigbe: Urinary sediment evaluation in hypertension

    agnosed hypertensive Nigerians have sub-clinical kidney

    damage, as evidenced by microscopic hematuria. There

    is a high false-negative rate with dipstick urinalysis among

    this patient population, which underscores the need for a

    routine examination of urinary sediment in addition to a

    dipstick test in the assessment of hypertensive patients. It

    is recommended, however, that supravital stains should be

    used for sediment identification in the absence of a phase

    contrast microscope.

    Financial support: No financial support.

    Conflict of interest statement: None declared.

    Address for correspondence:

    Timothy O. Olanrewaju, MD

    Division of Nephrology

    Department of Medicine

    University of Ilorin Teaching Hospital

    PMB 1459, Ilorin, Nigeria

    [email protected]

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    Received: July 25, 2009

    Revised: October 19, 2009

    Accepted: October 20, 2009