Considering Probiotics in CKD- Impact on Disease Progression and Enhancing Quality of Life

Chronic kidney disease
(CKD) is a “silent epidemic.” It is rarely diagnosed in its early
stages because clinical symptoms appear only after kidney function has been
irreversibly damaged.[1] CKD is the 17th most common cause of
disability and the 12th most common cause of mortality worldwide.[2]. Recent studies have
linked how diet and gut microbiota can help decrease CKD’s progression.[3] In
CKD patients, the natural intestinal microbiota changes, increasing aerobic
bacteria such as E. coli and
decreasing anaerobic bacteria such as Bifidobacterium.
Endotoxemia, induction of pro-inflammatory cytokines [C-reactive protein, IL-6,
IL-18, and TNF-alpha], and production of uremic toxins [urea, creatinine, and
other nitrogenous waste] via protein fermentation in the large intestine may
all contribute to the chronic inflammatory state in CKD patients and thus
aggravating CKD and reducing the quality of life.[4]

For the benefit of CKD
patients, probiotics are an emerging approach for restoring the altered gut
flora.[1] This review article aims to give a brief insight into how probiotics
can help decrease CKD progression and improve quality of life.

Diet, Gut microbiota, and CKD- Dissecting the
Intricate Link

In CKD, the colon
becomes the primary excretory organ to maintain homeostasis. Increased urea in
serum during CKD increases urea influx into the intestinal lumen, where
urease-producing bacteria hydrolyze it into ammonia and ammonium hydroxide,
increasing intestinal pH and promoting mucosal irritation and structural
alterations to the gut barrier. Such adaptive changes are linked to bacterial
translocation and endotoxemia, ultimately deteriorating CKD.[1]

Diet has long been
known to impact the progression of CKD. Excess sodium, protein, phosphate, or
oxalate in the diet may hasten the progression of CKD. Recently, it is
indicated in scientific evidence that the diet feeds both the human body and its
gut microbiota. Thus, diet may influence kidney disease through the direct
effects of specific nutrients on the human body and through modulation of gut
microbiota composition or metabolites produced by the gut microbiota from
ingested nutrients. e.g., dietary tyrosine is metabolized by the gut microbiota
to p-cresol, which human cells convert to the nephrotoxic compound p-cresyl
sulfate. Also, dietary tryptophan is metabolized by the gut microbiota to
indole, a precursor of uremic toxins with nephrotoxic potential such as indoxyl
sulfate [3]; thus, patients with
CKD may have to make dietary changes and
opt for a low-protein diet.[5]

Whirlwind Clinical Manifestations of CKD –
Deteriorating Quality of life

CKD worsens over time
if the patient doesn’t receive appropriate pharmacological and
non-pharmacological interventions, and CKD over time can result in a myriad of
health problems which include [6]

Raised risk of heart disease and stroke.Anemia, or a decreased red blood cell count,
can result in fatigue.Extra fluid in the body, which can result in
high blood pressure, leg swelling, or shortness of breath.Prone to infections resulting from weak
immunity.Low calcium and high phosphorus levels in the
blood can lead to bone and heart disease.High potassium levels in the blood can result
in an irregular or abnormal heartbeat and death.Over a period of time, CKD can progress, and
the condition of the kidneys deteriorate, leading to end-stage kidney disease
(ESKD)

All these
repercussions of CKD directly affect an individual, increasing morbidity, and
hospitalization and thus decreasing the quality of life and productivity.

Rationale for Applicability of Probiotics in
CKD

Probiotics are
“live microorganisms that, when provided in suitable proportions, impart a
health benefit on the host,” according to the World Health Organization
and the Food and Agriculture Organization of the United Nations. Probiotic
microorganisms like Bifidobacteria longum,
Lactobacillus acidophilus, Bacillus coagulans, etc., are some of
the most widely available forms of probiotics.

Certain probiotic
microorganisms can use urea, uric acid, creatinine, and other toxins to thrive.
Overburdened and impaired kidneys cause the accumulation of these poisonous
wastes in the bloodstream. Probiotic microorganisms multiply and metabolize
uremic toxins, allowing for greater diffusion from the circulating blood into
the bowel across the intestinal lining. These microbes are eventually excreted
in the faeces. By breaking down toxins, synthesizing vitamins, and defending
against infection, useful intestinal microbes can benefit health. Probiotics
can thus reduce the burden of toxic waste in CKD patients while improving the
quality of life.[2] Another advantage of probiotics is that they allegedly aid
in the growth of Bifidobacteria
populations, a genus known to play an important role in the function of the
intestinal mucosal barrier. The advantages of using probiotics in CKD patients
include a protective effect caused by lower levels of inflammatory markers.
Probiotic supplementation appears to be associated with significant reductions
in serum levels of proinflammatory cytokines TNF-, IL-5, and IL-6, as well as
endotoxins and increased levels of anti-inflammatory cytokine IL-10 by the production
of short-chain fatty acids (SCFA) [7], thus contributing to slowing the
progression of CKD and improving the quality of life.

Benefits of Probiotics in Chronic Kidney
Disease (CKD): Review of Clinical Evidence
[8]

A single-center,
double-blind, placebo-controlled, randomized cross-over trial was conducted on
30 patients having stage 3-4 CKD by Guida et al. The study lasted 4 weeks,
concluding that probiotics such as Streptococcus
thermophilus, L. acidophilus, B. longum, and B. coagulans could decrease the plasma p cresol level (0.78 vs 3.05
μg/ml, p < 0.05).A single-center,
double-blind, placebo-controlled trial for a period of 8 weeks was carried out
on 22 CKD patients by Natarajan et al. The study concluded that administering L. acidophilus and B. longum could increase the quality of life by reducing Indoxyl
glucuronide (-0.11 mg%, P = 0.058) and C reactive protein (-8.61 mg/L, P =
0.071).A single-center,
prospective, randomized, double-blind, cross-over, placebo control trial
conducted on 16 CKD patients of stages 3-4 were assessed by Ranganathan et al. The study was done for a period
of 6 months. It concluded that L.
acidophilus, S. thermophilus, and B. longum administration in CKD patients
decreased blood urea nitrogen (BUN) (-2.93 mmol/L vs 4.52 mmol/L, p =
0.002), uric acid concentration (24.70 micromol/L vs
50.62 micromol/L, p = 0.050) and increased quality of life.A single-center, non-randomized-placebo
controlled trial conducted on 22 individuals for a period of 5 weeks by
Takayama et al. concluded that
probiotics such as B. longum can
decrease the concentration of Indoxyl sulfate (3.5 +/- 1.3 mg/dL vs 4.9 +/- 1.7
mg/dL, P < 0.005).A multicenter,
prospective, randomised, double-blind, cross-over, placebo-controlled trial by
Ranganathan et al. included 46 patients with stage 3-4 CKD. The study was done
over a period of 6 months, and it concluded that probiotics such as L. acidophilus, S. thermophilus, and B.
longum can decrease the BUN (63%, P<0.05) and
can increase the quality of life (86%, P<0.05) among
CKD patients.A single-center,
observational trial conducted by Ando et al. on 27 subjects for a period of 6
months concluded that probiotics such as B.
longum could slow the progression of kidney disease.A multicenter,
double-blinded, placebo-controlled, randomised clinical trial was conducted on
42 CKD subjects by Viramontes-Hörner D et
al. to assess the efficacy of L.
acidophilus and Bifidobacterium.
The study was done over a span of 2 months. It concluded that probiotics could
improve gastrointestinal symptoms (anorexia, nausea, vomiting, heartburn,
stomachache, constipation and diarrhoea) and decrease plasma C reactive protein.

Points to Remember

CKD is one of the most underdiagnosed
conditions, which can directly hamper the quality of lifeStudies have shown how CKD and gut microbiota
are linked; dysbiosis can be caused by CKD, and improvement in the gut
environment can help decrease the progression of CKD.Probiotics can play a vital role in
maintaining the gut environment by decreasing the uremic toxins and increasing
the population of Bifidobacteria species
which can optimize the integrity of the intestinal mucosa.Probiotics also help decrease inflammatory
mediators and systemic inflammation and thus improve the quality of life among
CKD patients.

References

1. El-Kafoury, B.M., Saleh, N.K.,
Shawky, M.K. et al. Possible protective role of probiotic and symbiotic to
limit the progression of chronic kidney disease in 5/6th nephrectomised
albino rats. Bull Natl Res Cent 46, 252 (2022).
doi.org/10.1186/s42269-022-00936-4

2. Gharat, P.R., Vakharia, M.P.,
& Ranganathan, D.N. (2019). Specific Probiotics for Chronic Kidney
Disease: A Review.

3. Chiara Favero, Alberto Ortiz,
Maria D Sanchez-Niño, Probiotics for kidney disease, Clinical Kidney
Journal, Volume 15, Issue 11, November 2022, Pages 1981–1986, doi.org/10.1093/ckj/sfac056

4. I-Kuan Wang. The
Effect of Probiotics on Chronic Kidney Disease. ClinicalTrials.gov
Identifier: NCT03228563. July 25, 2017

5. Ko GJ, Obi Y, Tortorici AR,
Kalantar-Zadeh K. Dietary protein intake and chronic kidney disease. Curr
Opin Clin Nutr Metab Care. 2017 Jan;20(1):77-85. DOI:
10.1097/MCO.0000000000000342. PMID: 27801685; PMCID: PMC5962279.

6. Centers for Disease Control and Prevention. (2021). Chronic Kidney Disease Initiative. Retrieved from https://www.cdc.gov/kidneydisease/publications-resources/annual-report/ckd-related-health-problems.html

7. Fagundes RAB, Soder TF,
Grokoski KC, Benetti F, Mendes RH. Probiotics in the treatment of chronic
kidney disease: a systematic review. J Bras Nefrol. 2018
Jul-Sep;40(3):278-286. DOI: 10.1590/2175-8239-jbn-3931. Epub 2018 Jun 21.
PMID: 29958304; PMCID: PMC6533949.

8. Laetitia Koppe, Denise Mafra,
Denis Fouque, Probiotics and chronic kidney disease, Kidney International,
Volume 88, Issue 5, 2015, Pages 958-966, ISSN 0085-2538,
https://doi.org/10.1038/ki.2015.255

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