Prevalence of Urinary Tract Infection among Patients with Diabetes in Bangalore City

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1 Int. J. Emerg. Sci., 1(2), , June 2011 ISSN: IJES Prevalence of Urinary Tract Infection among Patients with Diabetes in Bangalore City Mehvish Saleem, Betty Daniel Department of Botany (Microbiology Unit) St. Josephs College PG and Research Centre Langford road Bangalore India Abstract. Urinary tract infections (UTI) are common in diabetic patients. The propensity of the infection can vary in different individuals especially when there is underreporting from the patients having a risk of acquiring infections. This investigation was based to evaluate the incidence of UTI in patients with DM. Between July , 1000 diabetic and non diabetic urine samples were collected. All urine samples were processed in the lab following standard laboratory protocol. Prevalence of UTI in the lower socioeconomic status was 56.4 and UTI in higher socioeconomic status was 51.6 and 48.4.Commonly recovered UTI isolates were E.coli, Enterococcus faecalis, Pseudomonas aeruginosa, and Staphylococcus aureus. UTI was alarming in diabetic patients belonging to the lower socioeconomic status. In type 1 diabetic patients E.coli (44) was the most prevalent cause of UTI. Varieties of factors are responsible for UTI in diabetic patients which include genetic susceptibility, and damaged immune response. The purpose of this study was to evaluate the prevalence of UTI among the diabetic patients and compare them with those of non diabetic ones from the areas of lower socio economic groups and higher socioeconomic group. Keywords: Diabetes mellitus (DM), Urinary Tract Infection (UTI), Bacteria, Prevalence 1 INTRODUCTION Urinary tract infections (UTIs) are the frequent infections observed in clinical practice and results in a significant morbidity and high medical costs. UTI is a common infection observed in diabetic patients. DM alters the genitourinary system where UTI can be a cause of severe complications ranging from dysuria (pain or burning sensation during Urination) organ damage and sometimes even death due to complicated UTI (pyeleonephritis). UTI is more widespread in women with DM than in non diabetic women as a consequence of debilitated immune system. The risk factors for UTI involve colonization with a different uropathogen in cases of recurrent UTI, glucosuria and impaired granulocyte function [45]. Diabetic patients are at a higher risk developing 133

2 Mehvish Saleem, Betty Daniel acute pyelonephritis, renal abscess, abnormalities of bladder scarring and pyelitis. People with diabetes have dysfunctional bladders which contract poorly. Women are prone to UTIs for reasons which are not well understood. [22] Every one woman develops UTI among five women. UTI is uncommon in men and contributes to have larger complications after initial infection. Ninety five percent of UTIs are caused by uropathogens which multiply at the notch of the urethra and migrate towards the bladder. UTI is a result of various factors which may trigger Infection. Recurrent UTI is a nasty infection in sexually active young women and patients with DM. Cystitis or bladder infection is commonly prevalent in women and young adolescent girls. The infection can be brief and acute (Cystitis) with classical symptoms of dysuria. In cases of continuous infection deeper layers of the bladder may be damaged (pyleonephritis). The risk of UTI increases with harmful changes in the immune system which also leads to the easier invasion and colonization in the lining of the bladder by Uropathogens. DM is also a leading a cause of overactive bladder or neurogenic bladder. It is a serious clinical problem for people with DM. Hospitalization for pyleonephritis occurs 15 times more frequently in diabetic patients. Symptomatic UTI may be present as a severe illness including higher frequency of bacteremia and bilateral renal involvement with pyleonephritis or unusual clinical presentations of emphysematous cystitis. Diabetic patients encounter urinary urgency and incontinence, during night. This condition is often manifested by the shape of painful urination and retention of urine in the bladder. DM also results in abnormalities of the host defense system that may result in a higher risk of developing infection. Immunologic impairments such as defective migration, and phagocytic alterations of chemotaxis in polymorphonuclear leukocytes is well marked in diabetic patients. 2. MATERIAL AND METHODS 2.1. Study Design Patients Specimen Collection. Clean voided midstream urine samples were collected in sterile uricols with the assistance of laboratory staff at their respective Hospitals and diabetic centers. Urine samples were processed in the laboratory within 2 h of collection. Diabetic patients living in slums were educated about the collection of urine sample to avoid contamination.urine samples in type 1 diabetic patients(100) were obtained from Janani Diabetic centre located in JPNagar Bangalore. Self prepared questionnaires were given to diabetic subjects to obtain information on age, history of urinary frequency, abdominal pain, Hypertension, Cardiovascular diseases, Lipidemia, and previous infections encountered. 134

3 International Journal of Emerging. Sciences, 1(2), , June 2011 Presumptive Identification of Uropathogens from Urine Samples. All urine samples were plated with 100 μl of urine sample using standard pour plate technique on Hi Chrome UTI Agar (Himedia pvt ltd India) and incubated at 37 C overnight for visible growth. Urine samples showing colony count more than 10,000Cfu/ml was considered to be significant for UTI [46].UTI isolates were identified following standard biochemical tests [47]. Results were not considered for more than three clinical isolates obtained on isolation and the sample was considered to be contaminated. Statistical Analysis. The Statistical software SPSS 15.0, Stata 8.0, MedCalc and Systat 11.0 were used for the analysis of the data. Results were calculated on the basis of number and percentages from the higher and Lower socioeconomic groups. P values were calculated using a 2 test. P <0.01 were considered to be statistically significant Results Diabetic Lower socioeconomic Status Group. Uropathogens were isolated from 140 males and 110 females. UTI isolates in diabetic males and females included E.coli 46 (32.9) 28 (25.5), E.faecalis 44(31.4), 32(29.1) P.aeruginosa 2(1.4) 10 (9.1), S.aureus 26(18.6) 22(20). UTI was found in 22 males (15.7) and 18 females (16.4) in patients with DM respectively. Table 1 shows the Uropathogens isolated urine samples in the diabetic Lower socioeconomic group. Table I Prevalence of UTI in Diabetic Low Socioeconomic status group. UTI Pathogens Prevalence of UTI (Males) Prevalence of UTI (Females) Total E.coli Enterococcus Faecalis P.aeruginosa S.aureus Patients with no UTI Total Table 2 shows the prevalence of UTI pathogens in diabetic Higher Socioeconomic group according to the gender in diabetic males and females. Commonly recovered UTI pathogens in males and females with DM included E.coli 18(13.8) 13(10.8) E.faecalis 32(24.6), 36 (30.0), P.aeruginosa 30(23.1) 135

4 Mehvish Saleem, Betty Daniel S.aureus 13(10), 24 (20) respectively. There was no prevalence of UTI found in 28.5 of males and25.8 of females. Table 2. Prevalence of UTI in Diabetic Higher Socioeconomic status group. UTI pathogens Prevalence of UTI Prevalence of UTI Total Isolates(Males) Isolates (Females) E.coli Enterococcus faecalis P.aeruginosa S.aureus Patients with no UTI. Total Table 3 shows the incidence of Uropathogens (Male and female) in DM type 1.The prevalence of E.coli was 22(44) in males and 15(30) in females, E.faecalis 10(20), 20(40), S.aureus 14(28), 8(16) respectively. 8 of males and 14 of females had no evidence of UTI. Table 3. Prevalence of UTI pathogens in Type1 diabetic patients. UTI pathogens Prevalence of UTI Prevalence of UTI Total Isolates(Males) Isolates (Females) E.coli E.faecalis P.aeruginosa S.aureus UTI Total Table 4 shows the comparison of results between the diabetic patients of the lower socioeconomic status and the with non diabetic control groups. The prevalence of E.coli was 74(29.6), E.Faecalis 76(30.4) P.aeruginosa 12(4.8) S.aureus48 (19.2) respectively. 40 (16)of patients had no evidence of UTI. Prevalence of Uropathogens in non diabetic patients was E.coli (19), E.Faecalis (15.3) P.aeruginosa (18), S.aureus (8.7).44.7 of non diabetic patients showed no evidence of UTI. 136

5 International Journal of Emerging. Sciences, 1(2), , June 2011 Table 4 Comparison of Prevalence of organism isolated between Diabetic and nondiabetic in Lower Socioeconomic status: UTI pathogens DM group n Diabetic Group P value E.coli =15.086;P<0.001** E. faecalis =11.427;P<0.001** P.aeruginosa =20.030;P<0.001** S.aureus =8.048; P<0.001** UTI =39.318;P<0.001** Total Table 5 shows the comparison of results between the diabetic patients of the higher socioeconomic status and the with non diabetic control groups. The prevalence of E.coli was 31 (12.4), E.Faecalis. 68 (27.2) P.aeruginosa 46 (18.4) S.aureus 37 (14.8) respectively. 68(27.2) of patients had no UTI. Prevalence of Uropathogens in non diabetic patients was significantly less when compared with diabetic patients E.coli (8.4), E.Faecalis (20) There was no prevalence of P.aeruginosa in the non diabetic group. The prevalence of S.aureus was 10.8).60.8 of non diabetic patients did not indicate any UTI. The results obtained from the two different groups of diabetic patients also suggest that the prevalence of UTI in the lower socioeconomic status was high. Table 5 Comparison of Prevalence of organism isolated between Diabetic and nondiabetic in Higher Socioeconomic status: UTI Pathogens DM Group n diabetic Group P value E.coli =2.146; P=0.143 E.faecalis =3.594; = P.aeruginosa =50.661; 0.001** S.aureus =1.792; P=0.181 UTI =57.273;P<0.001** Total

6 Mehvish Saleem, Betty Daniel Percentages E.coli, E.faecalis, P.aeruginosa, S.aureus, UTI Lower SES of diabetic Lower SES of control Prevalence of UTI between Diabetic and nondiabetic in Lower Socio Figure 1. Comparison of economic status (SES). Percentages E.coli, E.Feacalis, P.aeruginosa, S.aurues, UTI UTI pathogens Higher SES of diabetic Figure 2. Comparison of distribution of organism isolated between Diabetic and nondiabetic in Higher Socioeconomic status (SES). 4. DISCUSSION Our findings suggest that the relevant clinical epidemiological data which identify the prevalence of UTI in diabetic patients are lacking. Bangalore is fast growing developing city with a dense urban population. Many patients do not undergo regular diagnosis for DM unless they showcase the symptoms. Diabetes goes unnoticed in slums, as a consequence of poor economic status. Limited access to the hospitals in this economically weaker section leads to the Increase in DM. The treatment for DM appears to be costly for slum dwellers. Sometimes the treatment for diabetes such as Insulin Injections does not reach the patients living in slums leading to poor glycemic control. Many diabetic patients in the urban slums face unhygienic conditions, malnutrition and no proper sanitation making the situation 138

7 International Journal of Emerging. Sciences, 1(2), , June 2011 worse. Diabetic patients with UTI in slums use over the counter prescriptions which does not eradicate the infection but leads to recurrent Infections. The severe cases of UTI are untreated as a consequence of costly antibiotic treatment. We found UTI was significantly high in diabetic patients of the Lower socioeconomic status (Table 1) The prevalence of S.aurues was found high in type 2 diabetic females in the Lower socio economic group (20). The frequency of UTI in diabetic women as a result of S.aureus may also be attributed to frequent sexual activity and close proximity of vagina with Urethra [30]. Among the diabetic patients in the lower socioeconomic status E. coli was isolated from 32.9 diabetic males and 25.5 from female diabetic patients.pseudomonas spp was prevalent in. 1,4 males and 9.1 females. The incidence of P.aeruginosa in diabetic patients clearly indicates immune suppression by this opportunistic uropathogen which never causes any symptoms of UTI in the non diabetic subjects. The frequent incidence, prevalence, and severity of UTI in diabetic patients squabble for firm antibiotic chemotherapy. We suggest that future Clinical Investigations in DM should focus on how the infection differs from that in patients without DM. We also propose to emphasize on the character of glycosuria and risk of UTI. Diabetic patients with poor glycemic control have a higher tendency of E.coli adherence. [5], [16]. Enterococci could be a consequence of nosocomial UTI [17] Enterococcus feacalis was found to be the cause of 35 of UTI in hospital patients [18], [25]. Our results showed a close similarity with the above study of diabetic male subjects and 29.1 females had UTI as a consequence of Enterococci spp. in the lower socioeconomic status. This also signifies the prevalence of community acquired UTI. The prevalence of uropathogens was considerably less in patients with DM of the higher socioeconomic status Table2.The occurrence of E.coli was high in patients with DM type 1 when compared with the type 2 diabetic results. Patients with DM type 1 have a risk of acquiring bacteremia, with UTI as the most prevalent infection. This also exposes diabetic patients to higher mortality in community acquired infections when compared with patients without DM. This pattern of distribution of uropathogens could be incidental in nature with more confounding factors involved in the pattern of colonization, and additional investigations should be put forward to understand the biodiversity of UTI pathogens in patients with DM type1 and type2. 5. CONCLUSION UTIs are more frequent and are likely to have a more complicated course in patients with (DM). India is considered to be the diabetic capital of world and many factors contribute to the emergence of Diabetes in developing nations. The mechanisms, which potentially contribute to the greater incidence of UTI in these patients, are malfunctioning in the local urinary cytokine secretions and an increased adherence of bacteria to the cells of the Uroepithelial cells. confirmation is available on the best possible treatment of acute cystitis and pyelonephritis in patients with DM. Thus we suggest screening of UTI in diabetic patients is imperative. 139

8 Mehvish Saleem, Betty Daniel REFERENCES [1] Cooke DW, Plotnick L vember "Type 1 diabetes mellitus in pediatrics". Pediatr Rev 29 (11): [2] Saydah SH, Miret M, Sung J, Varas C, Gause D, Brancati FL 2001 "Postchallenge hyperglycemia and mortality in a national sample of U.S. adults". Diabetes Care 24 (8): [3] Rengards RT: Asymptomatic bacteriuria in sixtyeight diabetic patients. Am J Med Sci 1960, 239:15964.PubMed Abstract [4] Szucs S, Cserhati, Csapo G, Balazs V: The relation between diabetes mellitus and infections of the urinary tract.am J Med Sci 1960, 240: PubMed Abstract [5] Andriole VT: Asymptomatic bacteriuria in patients with diabetes enemy or innocent visitor? N Engl J Med 2002,347: PubMed Abstract Publisher Full Text [6] Huvos A, Rocha J: Frequency of bacteriuria in patients with diabetes mellitus. N Engl J Med 1959, 261:12136.PubMed Abstract. [7] Vejsgaard R: Studies on urinary infections in diabetics. I. Bacteriuria in patients with diabetes mellitus and in control subjects. Acta Med Scand 1966, 179: PubMed Abstract [8] Pometta D, Rees SB, Younger D, Kass EH: Asymptomatic bacteriuria in diabetes mellitus.n Engl J Med 1967, 276: PubMed Abstract [9] BS, Chen BT, Yu M: Prevalence and site of bacteriuria in diabetes mellitus. Postgrad Med J 1974,50(586):4979. PubMed Abstract [10] Bonadio M, Pulitanò L, Catania B, Marchetti P, Miccoli R, Navalesi R: Urinary tract infection in women with controlled diabetes. In Pyelonephritis. Volume : [11] Schmitt JK, Fawcett CJ, Gullickson G: Asymptomatic bacteriuria and hemoglobin A1. Diabetes Care 1986,9: PubMed Abstract [12] Kelestimur F, Unal A, Pasaoglu H, Basar E, Kilic H, Doganay M: Asymptomatic bacteriuria in patients with diabetes mellitus. Mikrobiyol Bul 1990, 24(2): PubMed Abstract [13] Geerlings SE, Stolk RP, Camps MJ, Netten PM, Collet TJ, Hoepelman AI: Asymptomatic bacteriuria may be considered a complication in women with diabetes. The Diabetes Mellitus Women Asymptomatic BacteriuriaUtrecht Study Group. Diabetes Care 2000, 23:7449. PubMed Abstract Publisher Full Text [14] Lye WC, Chan RK, Lee EJ, Kumarasinghe G: Urinary tract infections in patients with diabetes mellitus. J Infect 1992, 24: PubMed Abstract Publisher Full Text [15] Bonadio M, Meini M, Spitaleri P, Gigli C: Current microbiological and clinical aspects of urinary tract infections. Eur Urol 2001, 40(4): PubMed Abstract Publisher Full Text [16] Stapleton A: Urinary tract infections in patients with diabetes Am J Med 113Suppl 1A:80S84S. PubMed Abstract Publisher Full Text Ronald A, Harding G: Complicated urinary tract infections. Infect Dis Clin rth Am 1997, 11: PubMed Abstract Publisher Full Text [17]Boyko EJ, Fihn SD, Scholes D, Chen CL, rmand EH, Yarbro P: Diabetes and the risk of acute urinary tract infection among postmenopausal women. Diabetes Care 2002, 25(10):1778. PubMed Abstract Publisher Full Text 140

9 International Journal of Emerging. Sciences, 1(2), , June 2011 [18] PerezLuque EL, de la Luz Villalpando M, Malacara JM: Association of sexual activity and bacteruria in women with non.insulin dependent diabetes mellitus. J DiabetesComplications 1992, 6(4): PubMed Abstract Publisher Full Text [19] Brauner A, Flodin U, Hylander B, Ostenson C: Bacteriuria, bacterial virulence and host factors in diabetic patients. Diabet Med 1993, 10: PubMed Abstract [20] Zhanel GG, Nicolle LE, Harding GKM: Prevalence of asymptomatic bacteriuria and associated host factors in women with diabetes mellitus. The Manitoba Diabetic Urinary Infection Study Group. Clin Infect Dis 1995,21(2): PubMed Abstract [21] Conway PH, Cnaan A, Zaoutis T, Henry BV, Grundmeier RW, Keren R. Recurrent urinary tract infections inchildren risk factors and association with prophylactic antimicrobials. JAMA. Jul 11; 298(2):17986 [22] Patterson JE, Andriole VT. Bacterial urinary tract infections in diabetes. Infect Dis Clin rtham.1995;9: [PubMed] [23] Kass EH. Bacteriuria and the diagnosis of infections of the urinary tract. Arch Intern Med. 1957;100: [24] Zhanel GG, Harding GK, Nicolle LE. Asymptomatic bacteriuria in patients with diabetes mellitus. Rev Infect Dis.991;13: [25] Hansen RO. Bacteriuria in diabetic and non diabetic outpatients. Acta Med Scand. 1964; 176: [26] Vejlsgaard R. Studies on urinary infection in diabetics. I. Bacteriuria in patients with diabetes mellitus and in control subjects. Acta Med Scand. 1966;179: [27] Vejlsgaard R. Studies on urinary infection in diabetics. II. Significant bacteriuria in relation to longterm diabetic manifestations. Acta Med Scand. 1966;179: [28] Zhanel GG, Nicolle LE, Harding GKM, and the Manitoba Diabetic Urinary Infection Study Group. Prevalence of asymptomatic bacteriuria and associated host factors in women with diabetes mellitus. Clin Infect Dis. 1995;21: [29] Schmitt JK, Fawcett CJ, Gullickson G. Asymptomatic bacteriuria and hemoglobin A1. Diabetes Care. 1986;9: [36]Sawers JS, Todd WA, Kellett HA, et al. Bacteriuria and autonomic nerve function in diabetic women. Diabetes Care. 1986;9: [30] Wheat LJ. Infection and diabetes mellitus. Diabetes Care. 1980;3: [31] Schainuck LI, Fouty R, Cutler RE: Emphysematous pyelonephritis. Am J Med. 1968;44: [32] Lauler DP, Schreiner GE, David A. Renal medullary necrosis. Am J Med. 1960;29: [33] Mandel EE. Renal medullary necrosis. Am J Med. 1952;13: [34] Whitehouse FW, Root HF. Necrotizing renal papillitis and diabetes mellitus. JAMA. 1956; 162: [35] Sharkey TP, Root HF. Infection of the urinary tract in diabetes. JAMA. 1935;104: [36] Baldwin AD, Root HF. Infections of the upper urinary tract in the diabetic patient. N Engl J Med. 1940;223: [37] Forland M, Thomas V, Shelokov A. Urinary tract infections in patients with diabetes mellitus: studies on antibody coating of bacteria. JAMA. 1977; 238:

10 Mehvish Saleem, Betty Daniel [38] MacFarlane IA, Brown RM, Smyth RW, et al. Bacteraemia in diabetics. J Infection. 1986; 12: [39] Lee KH, Hui KP, Tan WC, Lim TK. Klebsiella bacteraemia: a report of 101 cases from National University Hospital, Singapore. J Hosp Infect. 1994; 27: [40] Carton JA, Maradona JA, Nuno FJ, et al. Diabetes mellitus and bacteraemia: a comparative study between diabetic and nondiabetic patients. Eur J Med. 1992;1: [41] Geerlings SE, Hoepelman AIM. Immune dysfunction in patients with diabetes mellitus (DM). FEMS Immunol Med Microbiol. 1999; 26: [42] Bagdade JD, Steward M, Walters E. Impaired granulocyte adherence. A reversible defect in host defense in patients with poorly controlled diabetes. Diabetes. 1978; 27: [43] lan CM, Beaty HN, Bagdade JD. Further characterization of the impaired bactericidal function of granulocytes in patients with poorly controlled diabetes. Diabetes. 1978;27: [44] Kaneshige H, Endoh M, Tomino Y, et al. Impaired granulocyte function in patients with diabetes mellitus Tokai J Exp Clin Med.1982; 7:7780. [45] Geerlings, S. E. (2008). Urinary tract infections in patients with diabetes mellitus: epidemiology, pathogenesis and treatment. Int J Antimicrob Agents31, S54 S57.[CrossRef][Medline] [46] Wilson, M. L. & Gaido, L. (2004). Laboratory diagnosis of urinary tract infections in adult patients. Clin Infect Dis 38, [CrossRef][Medline] [47] Collee, J. G., Duguid, J. P, Fraser, Marmion, B.P. (1989). Practical Medical Microbiology, 3rd edn. Edinburgh 142

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