Tuberculosis and the Kidney
Bibliographic record
Abstract
Tuberculosis of the kidney and urinary tract is, like other forms of the disease, caused by members of the Mycobacterium tuberculosis complex. By far the most common causative organism is the human tubercle bacillus, M. tuberculosis, but the bovine tubercle bacillus, M. bovis, occasionally can be responsible. The vaccine strain, Bacille Calmette-Gue[Combining Acute Accent]rin (BCG), also has been the cause of renal lesions as a complication of intravesical instillation of BCG for the treatment of superficial bladder cancer. The members of the M. tuberculosis complex are obligate pathogens and, together with M. leprae, differ from the many other species within the genus Mycobacterium, which are free-living environmental saprophytes and are commonly found in water, including piped water supplies. Some of these so-called environmental mycobacteria occasionally cause human disease, particularly in immunosuppressed individuals, including recipients of renal transplants (1). The kidney may be involved when environmental mycobacteria cause disseminated disease, such as that caused by M. avium in AIDS patients. Renal disease caused by environmental mycobacteria in nonimmunosuppressed individuals is exceedingly rare (2). However, because they occur in water, environmental mycobacteria readily contaminate the lower urethra and external genitalia and, thus, often are isolated from urine samples. Globally, tuberculosis is a common disease, with 8 to 10 million new cases annually and a rising incidence, particularly in regions with a high incidence of HIV infection. Most often the lung is affected, but, after lymphadenopathy, the most common form of nonpulmonary tuberculosis is genitourinary disease, accounting for 27% (range, 14 to 41%) of nonpulmonary cases in several surveys in the United States, Canada, and United Kingdom (3). In developed countries, nonpulmonary tuberculosis is relatively more common in patients from ethnic minority groups, the exception being genitourinary tuberculosis, which is uncommon in these groups. In the United Kingdom, the latter accounts for 5% of cases of nonpulmonary tuberculosis in ethnic minorities, mostly those of Indian subcontinent ethnic origin, compared with 27% of such cases in the European (white) population. This is, to some extent, age related: when patients of white and of Indian subcontinent ethnic origin were stratified by age, the incidence of genitourinary tuberculosis was similar in the two groups in each age band (4). Tuberculosis caused by M. bovis is now uncommon in industrially developed nations, accounting for fewer than 1% of all cases of tuberculosis. It is usually due to reactivation of old, dormant disease, although cases have occurred in younger, HIV-positive patients (5). In approximately 25% of cases caused by reactivation in older persons, the genitourinary system is involved (6). Such disease has a somewhat bizarre veterinary health significance because a number of farmers have infected cattle by urinating on hay in cowsheds (7). Clinical Features Classical Renal Tuberculosis Tuberculosis of the urinary tract is easily overlooked. Many patients present with lower urinary symptoms typical of “conventional” bacterial cystitis, and suspicions of tuberculosis are aroused only when there is no response to the usual antibacterial agents or when urine examination reveals pyuria in the absence of a positive culture on routine media. Other symptoms that sometimes occur include back, flank, and suprapubic pain; hematuria; frequency; and nocturia; these might also suggest conventional bacterial urinary tract infection. Renal colic is uncommon, occurring in fewer than 10% of patients, and constitutional symptoms such as fever, weight loss, and night sweats also are unusual. Only one third of patients have an abnormal chest x-ray. In one study, 18 of 25 physicians with renal tuberculosis presented only after advanced cavitating disease had developed (8). Indeed, the diagnosis sometimes is made for the first time at operation or post mortem. The diagnosis of tuberculosis of the urinary tract is based on the finding of pyuria in the absence of infection as judged by culture on routine media. In early disease, it often is possible on intravenous urography to detect changes in a single calyx (Figure 1) with evidence of parenchymal necrosis, and typically there is calcification on the plain film. In more advanced disease, urography will show calyceal distortion, ureteric strictures (Figure 2), and bladder fibrosis. Ultrasound examination of the urinary tract may reveal renal calyceal dilation and more overt evidence of obstruction.Figure 1: . (A) Plain film showing calcification in the lower pole of the right kidney. (B) Five-min film showing an abnormal calyx with some loss of renal substance. There was a sterile pyuria, and Mycobacterium tuberculosis was isolated from the urine.Figure 2: . (A) Plain film showing renal calcification. (B) Twenty-min film showing ureteric dilation and stricture and an irregular bladder wall. M. tuberculosis was isolated from the urine.Ultimately, a tuberculous kidney may become calcified and nonfunctioning. Not surprising, if the gross anatomic distortion is advanced and bilateral, the GFR will fall and, in some patients, there is progression to end-stage renal failure. Tuberculous Interstitial Nephritis It now is clear that tuberculosis can affect the kidney more insidiously. In one report, three patients with advanced renal failure, in whom imaging showed equal-sized smooth kidneys, were described (9). In none was tubercle bacilli found in the urine. Renal histology revealed chronic tubulointerstitial nephritis with granuloma formation in all three and caseation in two. In two, acid-fast bacilli were identified with appropriate stains. Two of the three patients had evidence of tuberculosis on chest x-ray, and one had tuberculous peritonitis. Subsequently, there have been additional reports of this atypical form of tuberculosis, which in the United Kingdom seems to occur particularly in individuals from the Indian subcontinent. When the diagnosis has been made while useful renal function remains, it sometimes has been possible to arrest the fall in GFR (Figure 3) or even produce improvement. In some of these patients, there is pyuria, but in others there is not.Figure 3: . Graph of reciprocal creatinine (mg/dl) against time in one patient to illustrate arrest of decline of renal function after treatment of renal tuberculosis. Bar indicates treatment with antituberculosis drugs and prednisolone for 6 mo.Tuberculosis and Glomerular Disease Chronic tuberculosis sometimes is complicated by amyloidosis, which, in India, is an important cause of renal disease (10). There are a number of case reports of tuberculosis associated with various forms of glomerulonephritis, but no firm associations have been established. There also is a case report of miliary tuberculosis complicated by focal proliferative glomerulonephritis: immune deposits were present but no granulomas (11). End-Stage Renal Disease Tuberculosis, although an uncommon cause of progressive renal failure, is an important one because, unlike many renal conditions, it is potentially preventable and easily treatable. Evidence as to the extent to which tuberculosis is a cause of end-stage renal failure worldwide is scanty. Whereas most of the world's tuberculosis is in developing countries, registries of patients with end-stage renal failure are mainly in the developed world, as are diagnostic methods for arriving at a renal diagnosis. For these reasons, there is little information on the contribution that tuberculosis makes to the burden of renal disease. In 1991, data obtained from the European Dialysis and Transplant Association registry revealed that 195 of 30,064 new patients (0.65%) had renal failure caused by renal tuberculosis, an incidence similar to that of previous years (12). The country with the highest incidence was Greece (4.51% of new patients), other important contributors being Portugal, Belgium, Spain, Italy, and Yugoslavia. In the United Kingdom, tuberculosis is very uncommon as a primary renal diagnosis; in April 2001, the national database contained 25,338 patients, 60 (0.24%) of whom had been assigned renal tuberculosis as their renal diagnosis (D. Ansell, personal communication, April 2001). From published data on primary renal diagnosis from the United States, Europe, and Australasia (13), it is clear that tuberculosis is more common in Europe as a primary renal diagnosis (2247 cases [0.7%]) than in either the United States (0.004%) or Australasia (0.16%). Hemodialysis and Peritoneal Dialysis There are a number of reports of tuberculosis developing in patients on regular hemodialysis. Commonly, the patient manifests fever, anorexia, and weight loss and usually either is known to have had pulmonary or other forms of tuberculosis or is a member of a high-risk ethnic or social group. Often the recrudescence is extrapulmonary, so it is likely that, in most cases, the disease is due to reactivation of past disease rather than a primary infection. In a study of more than 300 hemodialysis patients in St. Louis, Missouri, it was found that 48 of 307 patients tested had a positive tuberculin skin test. Chest radiographs were done, but no new cases of tuberculosis were found (14). There are fewer reports of tuberculosis in chronic ambulatory peritoneal dialysis (CAPD) patients, but there is no reason to suspect that the risk is any different from patients on hemodialysis. There are a number of reports of tuberculous peritonitis (15, 16), which is easier to detect in patients on CAPD than in those on hemodialysis. In Turkey, a region with a high incidence of tuberculosis, 4 of 70 children on CAPD developed tuberculosis—affecting the lung in 3 and the bone in 1 (17). Disease caused by environmental mycobacteria also occurs in hemodialysis patients; it usually becomes apparent as pulmonary or disseminated disease or sometimes as skin lesions. Some infections have occurred as the result of contamination of the dialysis machine by environmental mycobacteria. In patients on peritoneal dialysis, there have been reports of peritonitis; such an eventuality usually necessitates removal of the catheter and transfer of the patient to hemodialysis. Transplant Patients Tuberculosis is a serious complicating factor in renal and other forms of transplantation, with an incidence, depending on geographic region, of 0.35 to 15.0% (18). In most cases, the disease involves the lung, but the disease is disseminated in one third of cases. Patients who have had tuberculosis while on dialysis are at increased risk, and it should be remembered that immunosuppression can obscure the diagnosis by producing false-negative tuberculin tests (14). In Saudi Arabia, 14 cases of tuberculosis developed among 403 renal transplant patients, an incidence approximately 50 times higher than in the general population of that country (1). Infections caused by environmental mycobacteria also occur in transplant patients, accounting for 29% of patients with mycobacterial disease in one review series (1). Because the symptoms often are masked by the immunosuppression, diagnosis may be delayed and the mortality is high: approximately 30%. It is the policy of many renal transplant units to give isoniazid prophylaxis for 1 yr to patients who are thought to be at particularly high risk of developing active tuberculosis. It is possible, by following this policy, to prevent reactivation of tuberculosis. In a series of 633 renal transplant patients, there were no cases of tuberculosis among patients who received chemotherapy but 6 cases among 27 high-risk patients who did not receive chemotherapy (19). A retrospective study of 520 renal transplant patients from Turkey adds weight to this policy (20). Tuberculosis was diagnosed in 22 patients, a mean of 44.4 mo after transplantation. The pleuropulmonary form was the most common (54%). Despite treatment, six of the patients died, one of isoniazid toxicity. In contrast, 23 patients who were at risk of developing tuberculosis had been given isoniazid prophylaxis for 1 yr. None of the 23 developed tuberculosis, and in none was toxicity seen. In our unit, we give isoniazid for 1 yr to patients who are at risk of developing tuberculosis, but, clearly, differing risks have to be considered. There would be a case, on the one hand, for stopping the chemoprophylaxis in patients whose immuno-suppression is reduced early but, on the other hand, continuing the isoniazid longer if high levels of immunosuppression are needed beyond 1 yr. Genital Tuberculosis In men, the site most commonly involved is the epididymis, followed by the prostate. Testicular involvement is less common and usually is the result of direct invasion from the epididymis. It is generally believed that tuberculous prostatitis results from antegrade infection within the urinary tract; epididymitis, however, probably is the result of blood-borne infection because it often is an isolated finding without urinary tract involvement (21, 22). It is important to be aware that a high proportion, perhaps 50 to 75%, of men with genital tuberculosis have radiologic abnormalities in the urinary tract, so the urinary tract of all such patients should be investigated. In women, there is no close correlation between urinary tract and genital tuberculosis; indeed, renal tract tuberculosis accompanies lesions of the reproductive tract in fewer than 5% of cases. Hypercalcemia in Dialysis Patients There are a number of reports, in patients who are treated by chronic hemodialysis, of an association between both disseminated and genitourinary tuberculosis and hypercalcemia (23,24,25). In one case, hypercalcemia was not observed until the patient had been on dialysis for 8 mo and it coincided with the development of persistent fever (23). Calcitriol levels were elevated, but circulating levels of parathyroid hormone were not. The patient was found to have widely disseminated tuberculosis. Hypercalcemia also has been reported in a CAPD patient with tuberculous peritonitis (26). Hypercalcemia is widely known in patients who have disseminated tuberculosis and who do not have renal failure or renal involvement. In such patients, levels of calcitriol (1,25-(OH)2D3) are known to be elevated, presumably as a result of increased synthesis of this active form of vitamin D by activated macrophages within the granulomas (27). Laboratory Diagnosis A microbiologic diagnosis of tuberculosis usually is made by isolation of the causative organism from urine or biopsy material on conventional solid media or by an automated system such as radiometry. Acid-fast bacilli may be seen on microscopy of centrifuged urine, but care must be taken when very few bacilli are seen, because these may be environmental mycobacteria that contaminate the lower urethra. Full technical details are given by Collins et al. (28). In recent years, nucleic-acid amplification techniques, such as PCR, have been investigated extensively for the detection of M. tuberculosis and other mycobacteria in clinical specimens, notably sputum. Relatively few studies have specifically evaluated PCR for detection of genitourinary tuberculosis, and these show the technique to be sensitive and specific, although some urine specimens contain inhibitory substances (29, 30). In addition, PCR has been used to detect mycobacterial DNA in urine in cases of HIV-related disseminated tuberculosis (31). Pathology Tuberculosis may involve the kidney as part of generalized disseminated infection or as localized genitourinary disease. The morphology of the lesions depends on the site of infection, the virulence of the and the immune of the Renal as of The kidney is involved in miliary tuberculosis blood-borne miliary are seen the renal most in the The lesions to 3 in and usually are or they of with or without and often contain usually can be within these lesions but sometimes are to Renal function usually is not in these patients. When the patient is the granulomas may be less and may be more readily is seen less When immunosuppression is and in cases in which the organism is one of the environmental such as M. the lesions may be more and than the usual miliary the response of with with is not a In some patients with pulmonary or disseminated tuberculosis, there is evidence of renal failure without typical miliary involvement or localized genitourinary lesions. In these cases the Tuberculous Interstitial biopsy has usually but not in all cases with The evidence that the renal is due to a of infection and renal is arrest of decline or even in function with a of antituberculosis treatment and (Figure Tuberculosis The kidney usually is infected by of bacilli from a of infection in the In most cases, at the time of there is no evidence of active pulmonary disease, although there may be clinical or radiologic evidence of past infection, that renal involvement occurs as a result of reactivation after a of renal tuberculosis usually but post studies in the first of the that the disease is a tuberculous in the lung to the system by of the of a usually a may be disseminated the However, the bacilli have and generally to only in a number of including the epididymis, bone and particularly the In the the site of is the renal the lesions are with necrosis, to The infection may cause of the by and may (Figure to the renal a tuberculous that may even to a also known as a or kidney (Figure within the renal with calcification in of cases, as renal or ureteric in to of cases the the producing and lesions associated with The clinical of an renal include The renal lesions may the renal and produce a which can a involvement also may produce irregular ureteric strictures and to that ureteric and sometimes may be due to tuberculosis may prevent an if active treatment, including of can be early bacterial infection of the urinary tract is may as a complication of chronic and infection of the renal and may even after treatment of the active tuberculous This is a risk factor for the development of in chronic . Tuberculous infection renal with associated also the dilation and of the which also is . Tuberculous with and renal parenchymal to three of of tuberculous bladder infection are associated with renal infection, although in some cases tuberculous is believed to be due to from the epididymis. mycobacterial commonly is by instillation of BCG for the treatment of in and superficial bladder cancer. this only a superficial cystitis, but sometimes the is more of disseminated infection have been and ureteric involvement with ureteric was observed in cases in a series Renal involvement was found in of the patients in this presumably from infection rather than the lesions caused by BCG are from those seen in tuberculosis, and caseation may be may be by such as Tuberculosis and 10% of all cases of tuberculosis worldwide in were HIV but in the was as high as in some The incidence is to in and also in Tuberculosis was the cause of in approximately of the 3 million patients who were of AIDS in In those who are only the disease that in In the more particularly those with of or a high and a tuberculin the disease often is disseminated and the kidney is involved with various including The incidence of renal involvement may be higher than In an study in India, of from patients who of AIDS showed evidence of infection, including cases of tuberculosis In a similar study in renal disease was in of on AIDS infection was the cause of the renal disease in cases, with being due to M. tuberculosis Tuberculosis and D There is evidence that a fall in D levels immune and to the of tuberculosis In a population of of origin in those with D levels had an increased risk of active tuberculosis The between D levels and the risk of genitourinary tuberculosis in this population is as this form of tuberculosis is relatively uncommon in this group. of Tuberculosis antituberculosis are in all forms of tuberculosis. are based on an of treatment in which, and and these all tubercle This is followed by a in which only and isoniazid are with the of the few For all must be and because a failure to with is the cause for treatment failure, the has the of direct of such easier for both patient and the drugs may be given or the of are from the In recent years, there has been a in the incidence of tuberculosis, which, by is caused by bacilli to and with or without to other drugs the of at drugs that are on the of from and are less and often more than the of is based on response but may be 18 mo or longer to the treatment of tuberculosis in patients with renal and may be given in because they are either in the or to that are not by the kidney. By contrast, care is in the of other and because these are the kidney. which may be and reduced should be given to the 25 three times if the GFR is between 50 and and if it is between and 50 and other are and and should be if possible in patients with of renal those on because they have a high risk of is an uncommon complication of isoniazid and usually is preventable by the of to 50 A few patients on hemodialysis have developed that did not to but the when isoniazid was the of of a of including and which often are given to transplant patients. of of and in such patients is additional complication is in HIV-positive patients who are active because these drugs with it is that be given of and that the of be to mo may so the most recent by the for Disease and should be is in cases of advanced disease complicated by or and for bladder of or lesions in is of ureteric by or may in patients with renal renal and a GFR of more than The treatment of disease caused by environmental mycobacteria depends on the in of the should be from national mycobacteria Tuberculosis is a common disease worldwide and as has many for the In developed nations, tuberculosis is relatively uncommon, but the risk of the disease is increased in immunosuppressed individuals, including patients on dialysis and recipients of kidney The and symptoms of renal tuberculosis those of other infections of the so diagnostic may prevent Diagnosis is not but in tests are very to for of kidney specimens from the Pathology of St.
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.001 | 0.002 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.001 | 0.000 |
| Bibliometrics | 0.001 | 0.001 |
| Science and technology studies | 0.001 | 0.001 |
| Scholarly communication | 0.002 | 0.001 |
| Open science | 0.000 | 0.001 |
| Research integrity | 0.002 | 0.003 |
| Insufficient payload (model declined to judge) | 0.013 | 0.002 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".