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Medical Journal of the Islamic Republic of Iran logoLink to Medical Journal of the Islamic Republic of Iran
. 2013 Feb;27(1):17–22.

Evaluation of liver and kidney function in favism patients

Akbar Dorgalaleh 1, Muhammad Shahid Shahzad 2, Mohammad Reza Younesi 3, Esmaeil Sanei Moghaddam 4, Mohammad Mahmoodi 5, Bijan Varmaghani 6, Zahra Kashani Khatib 7, Shaban Alizadeh 8,
PMCID: PMC3592938  PMID: 23483616

Abstract

Background

G6PD deficiency is the most common enzymopathy of red blood cells. The clinical symptoms of favism are jaundice, hematuria and haemolytic anaemia that seem to affect liver and kidney in long term. Thus we evaluate kidney and liver function of favism patients in an endemic area of the disease with a high rate of fava beans cultivation.

Methods

This study was performed on favism patients and healthy controls referring to Iranshahr central hospital. Liver and kidney function tests were performed.

Results

The results showed a statistically significant difference between these two groups (p <0.05) for liver function tests, (AST, ALT and ALP), but not for renal tests (BUN and creatinine) (p >0.05).

Conclusion

Due to abnormalities were seen in the liver function tests of these patients, we suggest that these tests be regularly performed for favism patients who are constantly exposed to oxidant agents.

Keywords: G6PD, Favism, Liver, Kidney

Introduction

Glucose-6-phosphate dehydrogenase (G6PD) (E.C.1.1.1.49) is the key regulatory enzyme in the hexosemonophosphate shunt that catalyzes the oxidation of glucose 6- phosphate to 6-phosphogluconolactone (1, 2). This first and rate-limiting step of shunt is associated with production of nicotinamide adenine dinucleotide (NADPH) that is required for the generation of reduced glutathione, which is important for the protection against oxidative damages (3).

More than 442 variants of human G6PD are known (4); many of them are associated with anemia resulting from the impaired ability of the erythrocyte to respond to toxic stress (2, 5).

Precise molecular characterization of the G6PD gene showed that these 442 variants correspond to only 140 mutations. These mutations cause G6PD deficiency, a common enzymopathy affecting over 400 million people worldwide (6, 7). The disease can cause neonatal jaundice, drug- or infection-induced hemolytic crisis, favism, and nonspherocytic hemolytic anemia (4, 8). According to the level of enzyme activity, World Health Organization classified variants of G6PD to five groups (9).

Mediterranean variant with an estimated prevalence of 5% is the most common variant in Southern Europe, Middle East and India. Rate of incidence of Mediterranean mutation in Turkey, Iran, and India are 80%, 69% and 60.4% respectively; In Pakistan and Saudi Arabia the Mediterranean mutation is the prevalent variant (10, 11).

This variant of G6PD is often associated with favism, an acute hemolytic crisis induced by ingestion of fava beans (Vicia faba) by individuals deficient in glucose-6-phosphate dehydrogenase (12). Vicine and convicine as natural occurring toxic compounds in Vicia faba are involved in the formation of hemolytic anemia (13).

Clinical symptoms of favism are pallor, jaundice, hematuria, and acute hemolytic anemia that occurs suddenly 24 to 48 hours after consumption of fava beans. Depletion of reduced glutathione and impairment of some important enzymes induce oxidative stress in G6PD-deficient red blood cells and lead to acute hemolytic anemia (1419).

Although the typical presentation of the disease is extravascular hemolysis, intravascular hemolysis also occurs (2022). Intravascular hemolysis is the destruction of red blood cells in the circulation with the release of cell contents such as hemoglobin into plasma (23, 24). Then free plasma hemoglobin is filtered through the kidney and cause hemoglobinuria that is one of the most prominent clinical signs of excessive intravascular hemolysis and can cause renal failure (2527).

In the other hand, extravascular hemolysis in favism occurs when altered RBCs during oxidative damage are phagocytized by macrophages in the spleen, liver and bone marrow; Therefore, free hemoglobin is not released into plasma (20, 22, 28).

Eventhough some believe that the breakdown of hemoglobin by the reticuloendo- thelial system causes increase in plasma bilirubin, others say that this increase, is largely the result of an impairment of liver function caused by G6PD deficiency in the liver (29, 30).

In spite of high prevalence of favism in many regions of Iran, fava is planted as a rich source of protein in these areas and since ingestion of fresh, dried or frozen forms of beans and even inhaling of its pollen can be associated with hemolytic events, favism patients can experience these episodes during the entire year.

It seems that frequent experience of these hemolytic episodes can have adverse effects on kidney and liver as the main organs involved in the hemolytic processes.

Thus the purpose of the present investigation is to evaluate the kidney and liver functions in favism patients by assessment of serum parameters implicate these organs status.

Methods

This study was performed on 55 blood samples taken from individuals referring to Iranshahr central hospital between January 2012 and September 2012 and their G6PD deficiency tests were positive by fluorescent spot method (Kimia Pagouhan lot no 90607).

Ethics approval and patient consent statements were taken from all patients.

Short draw or hemolyzed samples and also sample of patients with history of liver and kidney disorders were excluded from the study and on remained samples, deficiency was subsequently confirmed by quantitative enzyme assays according to the manufacturer instructions (Biolabo-France).

Then alanine aminotransferase (ALT) (pars azmun lot no. 90002), aspartat amino transferase (AST)) (pars azmun lot no. 90005) and alkaline phosphatase (ALP) (pars azmun lot no. 90002) for assessment of liver function and creatinine (pars azmun lot no. 90009) and Blood urea nitrogen (BUN) (pars azmun lot no. 90009) for evaluation of kidney function were performed by Mindray chemistry analayzer (BS-200 China). Tests were also performed on an additional 60 random G6PD non- deficient individuals as control.

Statistical analysis

Obtained data of study was analyzed by Statistical Package for Social Science (SPSS) software. Statistical independent t test was used to evaluate the significance of differences between two groups in mean of continuous variables. P < .05 was considered statistically significant.

Result

In the study group of 55 patients, 44 were men and 11 were women, with an average age of 25 (SD = 12) years (range 1-47). In the control group of 60 patients, 46 were men and 14 were women, with an average age of 28 (SD = 11) years (range 3-51). Comparison among mean of some liver function tests in G6PD deficient and control groups showed statistically significant difference (P < 0.05). Serum AST, ALT and ALP were significantly elevated in patients than control group (Fig 1).

Fig. 1.

Fig. 1

Comparison among mean of some liver function tests in G6PD deficient and control groups, represents significance at the p = 0.0001 level for AST(U/L), significance at the p = 0.001 level for ALT (U/L) and significance at the p < 0.05 level for ALP (U/L)test.

Comparison between mean of kidney function tests in these two groups did not show any statistically significant difference (p > 0.05) (Fig 2).

Fig. 2.

Fig. 2

Comparison between mean of kidney tests in G6PD deficient and control groups represents no statistically significance different (p > 0.05). Numbers shown on unit of mg/dl.

Discussion

Favism is a disease prevalent in Mediterranean countries and characterized by acute hemolytic anemia following ingestion of fava beans. The typical features of the disease are jaundice, hematuria and hemolytic anemia (14).

The fava beans are also common cultigens of Mediterranean area that can aggravate the disease in the G6PD deficient patients in this area. Since all types of fava beans can induce hemolytic episodes, favism patients can experience these episodes during the entire year (31, 32).

Occurrence of these frequent mild or severe episodes of hemolysis can, over time, lead to more serious complications, particularly in liver and kidney as the two main organs involved in the hemolytic process (25, 26, 33).

This study hypothesizes that in areas with endemic culture of fava beans, favism patients may be impaired in the performance of these two organs. The results of this study partly confirmed this theory about liver, because means of liver function tests, AST, ALT and ALP were significantly higher in the case group than in the control group (64.2 IU/L vs 22.1 IU/L, p < 0.0001, 27.5 IU/L vs 19.8 IU/L, p < 0.001 and 366.4 IU/L vs 186.3 IU/L, p < 0.002 respectively). Although mean of ALT in patient group located in the normal range (Table 1). These elevated liver enzymes can be resulted from occurrence of recurrent hemolytic episodes that involve liver because a part of this hemolytic process can be extravascular. Moreover G6PD deficiency in liver can be a probable cause of liver complication in these patients but this claim require more investigations.

Table 1.

Statistical analysis of tests conducted on the patients and control groups. All liver function tests Showed statistically significant difference between these two groups(p < 0.05), while kidney tests did not Show any significant difference(p > 0.05).

Number Mean SD Min Max p value
AST (U/L) patient 55 64.2 36.9 12 179 0.0001
Control 60 22.1 6.7 4 40
ALT (U/L) patient 55 27.5 16.4 7 84 0.001
Control 60 19.8 8.2 9 39
ALP (U/L) patient 55 366.4 130.6 100 770 <0.05
Control 60 186.3 85.6 93 670
BUN (mg/dL) patient 55 19.4 9.2 10 52 >0.05
Control 60 19.8 6.4 10 42
CR (mg/dL) patient 55 0.75 0.25 0.4 1.4 >0.05
Control 60 0.79 0.19 0.4 1.2

We did not observe any significant correlation between age and liver function enzyme levels (p > 0.05).

On the other hand, BUN and creatinine as renal tests didn't show statistically significant difference between patient and control groups (19.4 vs 19.8, p > 0.05 and 0.75 vs 0.79, p > 0.05) (Table 1).

Our observations about liver function tests are in accordance with some other studies such as Alavis et al that reported elevated levels of AST in majority and ALT in some favism patients (34).

Muhammad Anees et al in a case report study showed high levels of AST and ALT in a G6PD deficient patient (35). But our results was incompatible with findings of those studies that claimed that tests are normal in these patients (36). It seems that this incompatibility originates from some features of their studies such as sampling time or study region.

Our study was performed in an endemic region with 24% frequency of G6PD deficiency and high cultivation of fava bean that can lead to induction of frequent hemolytic episodes in the patients (37). Moreover we found significant increase in serum ALP in case than control group that may implicate effects of hemolytic episodes on liver or gallbladder.

In this study we found non-significant disparity in kidney function tests between case and control group that is incompatible with some studies showed elevated levels of these elements (35). This is due to their samples that were collected during hemolytic crisis whereas our sampling was not in this situation.

Conclusion

According to the results of this study and life style in these regions about consumption of beans as a traditional cheap and rich source of protein, we suggest that liver function tests be regularly performed for favism patients who constantly were exposed to fava bean or other oxidant agents and their hemolytic complications were recognized. With early diagnosis of liver complication and use of extensive and regular medical cares, development of liver dysfunction can be prevented.

Moreover Vicine and convicine can be eliminated from the fava bean substrate by microbial and Fungal enzymes or other available methods to facilitate use of this source of protein (38).

References

  • 1.Frederiks WM, Bosch KS, De Jong JSSG, Van Noorden CJF. Post-translational regulation of glucose-6-phosphate dehydrogenase activity in (pre) neoplastic lesions in rat liver. Journal of Histochemistry & Cytochemistry. 2003;51(1):105. doi: 10.1177/002215540305100112. [DOI] [PubMed] [Google Scholar]
  • 2.Kwok CJ, Martin ACR, Au SWN, Lam V. G6PDdb, an integrated database of glucose-6-phosphate dehydrogenase (G6PD) mutations. Human mutation. 2002;19(3):217–24. doi: 10.1002/humu.10036. [DOI] [PubMed] [Google Scholar]
  • 3.Lee JW, Choi AH, Ham M, Kim JW, Choe SS, Park J, et al. G6PD up-regulation promotes pancreatic beta-cell dysfunction. Endocrinology. 2011;152(3):793–803. doi: 10.1210/en.2010-0606. [DOI] [PubMed] [Google Scholar]
  • 4.Mohanty D, Mukherjee MB, Colah RB. Glucose–6–phosphate dehydrogenase deficiency in India. Indian Journal of Pediatrics. 2004;71(6):525–9. doi: 10.1007/BF02724295. [DOI] [PubMed] [Google Scholar]
  • 5.Roth E, Jr, Schulman S. The adaptation of Plasmodium falciparum to oxidative stress in G6PD deficient human erythrocytes. British journal of haematology. 1988;70(3):363–7. doi: 10.1111/j.1365-2141.1988.tb02495.x. [DOI] [PubMed] [Google Scholar]
  • 6.Costa E, Cabeda J, Abreu M, Silva A, Morais L, Alexandrino A, et al. Glucose-6-phosphate dehydrogenase deficiency in 2 girls. Acta médica portuguesa. 1999;12(7-11):283. [PubMed] [Google Scholar]
  • 7.Jamshidi N, Wiback SJ, Palsson BØ. In silico model-driven assessment of the effects of single nucleotide polymorphisms (SNPs) on human red blood cell metabolism. Genome research. 2002;12(11):1687–92. doi: 10.1101/gr.329302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Ho H, Cheng M, Chiu D. G6PD-an old bottle with new wine. Chang Gung Medical Journal. 2005;28(9):606. [PubMed] [Google Scholar]
  • 9.Phompradit P, Kuesap J, Chaijaroenkul W, Rueangweerayut R, Hongkaew Y, Yamnuan R, et al. Prevalence and distribution of glucose-6-phosphate dehydrogenase (G6PD) variants in Thai and Burmese populations in malaria endemic areas of Thailand. Malar J. 2011;10:368. doi: 10.1186/1475-2875-10-368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Al-Musawi BMS, Al-Allawi N, Abdul-Majeed BA, Eissa AA, Jubrael JMS, Hamamy H. Molecular characterization of glucose-6- phosphate dehydrogenase deficient variants in Baghdad city-Iraq. BMC Blood Disorders. 2012;12(1):4. doi: 10.1186/1471-2326-12-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Warsy AS, El-Hazmi MAF. G6PD deficiency, distribution and variants in Saudi Arabia: an overview. Annals of Saudi Medicine. 2001;21(3/4):174–7. doi: 10.5144/0256-4947.2001.174. [DOI] [PubMed] [Google Scholar]
  • 12.Noori-Daloii M, Najafi L, Ganji SM, Hajebrahimi Z, Sanati M. Molecular identification of mutations in G6PD gene in patients with favism in Iran. Journal of Physiology and Biochemistry. 2004;60(4):273–7. doi: 10.1007/BF03167073. [DOI] [PubMed] [Google Scholar]
  • 13.Donath R, Kujawa M. The degradation of vicine and convicine in field bean meal by selected bacterial strains. Die Nahrung. 1991;35(5):449. doi: 10.1002/food.19910350506. [DOI] [PubMed] [Google Scholar]
  • 14.Arese P, Mannuzzu L, Turrini F. Pathophysiology of favism. Folia haematologica. 1989;116(5):745. Leipzig, Germany: 1928. [PubMed] [Google Scholar]
  • 15.Ganzoni AM. Biological thinking as the basis of clinical hematology. Pernicious anemia, sickle cell anemia, thalassemia and favism as examples. Schweiz Rundsch Med Prax. 1971 May 4;60(18):555–61. [PubMed] [Google Scholar]
  • 16.Kattamis C, Kyriazakou M, Chaidas S. Favism: clinical and biochemical data. Journal of medical genetics. 1969;6(1):34–41. doi: 10.1136/jmg.6.1.34. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Pazzi A, Accardo G, Aleotti A, Saletti G. Scanning electron microscopic study of the morphological changes induced by acetylsalicylic acid in therapeutic doses in the red blood cells of a patient with a very severe G6PD deficiency and clinical manifestations of favism. Giornale di clinica medica. 1980;61(6):435. [PubMed] [Google Scholar]
  • 18.Rojas J, Dujisin K, Calvo C. Clinical study of 3 cases of favism. Revista médica de Chile. 1982;110(12):1219. [PubMed] [Google Scholar]
  • 19.Yang XY. Epidemiological, clinical and laboratory studies of favism. Zhonghua Yi Xue Za Zhi. 1982 May;62(5):276–81. [PubMed] [Google Scholar]
  • 20.Beutler E, Laubscher K. Glucose 6-phosphate dehydrogenase deficiency. Clinical studies in medical biochemistry. 1997:91. [Google Scholar]
  • 21.Chan D. Glucose-6-phosphate dehydrogenase deficiency: correlation between the genotype, biochemistry and phenotype. Annals of the Academy of Medicine, Singapore. 2008;37(12 Suppl):81. [PubMed] [Google Scholar]
  • 22.Fischer T, Meloni T, Pescarmona G, Arese P. Membrane cross bonding in red cells in favic crisis: A missing link in the mechanism of extravascular haemolysis. British journal of haematology. 1985;59(1):159–69. doi: 10.1111/j.1365-2141.1985.tb02976.x. [DOI] [PubMed] [Google Scholar]
  • 23.Burwell EL, Kinney TD, Finch CA. Renal damage following intravascular hemolysis. New England Journal of Medicine. 1947;237(18):657–65. doi: 10.1056/NEJM194710302371802. [DOI] [PubMed] [Google Scholar]
  • 24.Luzzatto L. Glucose 6-phosphate dehydrogenase deficiency: from genotype to phenotype. Haematologica. 2006;91(10):1303–6. [PubMed] [Google Scholar]
  • 25.Chugh K, Singhal P, Sharma B, Mahakur A, Pal Y, Datta B, et al. Acute renal failure due to intravascular hemolysis in the North Indian patients. The American journal of the medical sciences. 1977;274(2):139. doi: 10.1097/00000441-197709000-00004. [DOI] [PubMed] [Google Scholar]
  • 26.Panich V, Sungnate T, Na-Nakorn S. Acute intravascular hemolysis and renal failure in a new glucose-6-phosphate dehydrogenase variant: G-6-PD Siriraj. Journal of the Medical Association of Thailand= Chotmaihet Thangphaet. 1972;55(12):726. [PubMed] [Google Scholar]
  • 27.Wyszyńska T, Mocarska M. Case of recurrent acute renal failure caused by intravascular hemolysis with hemoglobunuria. Pediatria polska. 1977;52(9):1029. [PubMed] [Google Scholar]
  • 28.Gerlach U, Losse H, Schmidt CG. Contribution to the recognition of intravascular hemolysis as a cause of acute renal failure. Klin Wochenschr. 1961 Feb 15;39:195–7. doi: 10.1007/BF01482952. [DOI] [PubMed] [Google Scholar]
  • 29.Blackburn C, Hensley W, Grant DK, Wright F, Slarke B. Studies on intravascular hemolysis in man. The pathogenesis of the initial stages of acute renal failure. Journal of Clinical Investigation. 1954;33(6):825. doi: 10.1172/JCI102954. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Mehta A, Mason PJ, Vulliamy TJ. Glucose-6-phosphate dehydrogenase deficiency. Best Practice & Research Clinical Haematology. 2000;13(1):21–38. doi: 10.1053/beha.1999.0055. [DOI] [PubMed] [Google Scholar]
  • 31.Cutillo S. Favism, hemolytic crises and severe jaundice of the newborn infant in the population with increased G-6-PD deficiency. Pediatria (Napoli). 1972 Sep 30;80(3):vi–viii. [PubMed] [Google Scholar]
  • 32.Kattamis C, Karambula K, Ioannidou V, Hatzikou V. Jaundice and bilirubin levels in Greek children with favism. Archives of disease in childhood. 1976;51(3):233–5. doi: 10.1136/adc.51.3.233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Minucci A, Concolino P, De Luca D, Giardina B, Zuppi C, Capoluongo E. A prolonged neonatal jaundice associated with a rare G6PD mutation. Pediatric blood & cancer. 2009;53(3):475–8. doi: 10.1002/pbc.22046. [DOI] [PubMed] [Google Scholar]
  • 34.Alavi S, Nozad S, Hoseini M. Clinical and laboratory findings in Favism. Iranian Journal of Pediatrics. 2005;15(1):13–20. [Google Scholar]
  • 35.Anees M, Mumtaz A, Rizwan SM, Amin J, Moin H, Sharif MM. Hematuria: a rare presentation of G6PD deficiency. Gomal Journal of Medical Sciences. 2004;3(1) [Google Scholar]
  • 36.Kaur A, Doomra M, Kakkar N, Dhanoa J. Jaundice and Cola-Colored Urine in a Young Indian Boy. Lab Medicine. 2006;37(7):422–4. [Google Scholar]
  • 37.Nakhaee A, Salimi S, Zadehvakili A, Dabiri S, Noora M, Rezaei M, et al. The Prevalence of Mediterranean Mutation of Glucose-6-Phosphate Dehydrogenase (G6PD) in Zahedan. 2012;14(3):39–43. [Google Scholar]
  • 38.Donath R, Kujawa M. The degradation of vicine and convicine in field bean meal by selected bacterial strains. Nahrung. 1991;35(5):449–53. doi: 10.1002/food.19910350506. [DOI] [PubMed] [Google Scholar]

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