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Temporary Glucose - 6 phosphate dehydrogenase enzyme deficiency, an additional risk factor for invasive fungal
Sampa Ghose1, Christine Wilson2, Preity Sharma3
1Department of Medical Oncology, Dr. BRA-Institute Rotary Cancer Hospital, AIIMS, New Delhi, India. sampaghose@gmail.com.
Abstract:
Invasive fungal infections (IFI) represent a major threat to acute myeloid leukemia (AML) patients, especially after induction chemotherapy. Intense chemotherapeutic drugs further weaken the immune function of AML patients which increases their susceptibility to life-threatening fungal infection, including invasive aspergillosis (IA). At present, there is no single reliable serological marker or method to predict accurately the risk of IA after induction chemotherapy. We hypothesized that some anti-cancer medicines and antibiotics may trigger temporary Glucose-6-Phosphate Dehydrogenase (G6PD) level which may increase the risk of fungal infection. In this study, we found that the serum galactomannan (GM) level was high in AML patients during IA and decreased in patients who recovered from IA. Along with the serum GM level, the level of G6PD was measured during IA and recovery. We found that AML patients had reduced serum G6PD levels during IA and experienced restoration of G6PD levels upon recovery in paired samples. Interleukin-6 (IL-6) was found to be higher in serum during fungal infection and positively correlated with the level of lactate dehydrogenase (LDH). Overall, monitoring G6PD levels along with IL-6 and GM in serum may be helpful in predicting IFI in AML patients.
Insights
Monitoring Glucose-6-Phosphate Dehydrogenase (G6PD) levels alongside Interleukin-6 (IL-6) and galactomannan (GM) may help predict invasive fungal infections (IFI) in acute myeloid leukemia (AML) patients post-chemotherapy.
Area of Science:
- Hematology
- Mycology
- Immunology
Background:
- Invasive fungal infections (IFI) pose a significant risk to acute myeloid leukemia (AML) patients, particularly after induction chemotherapy.
- Chemotherapy-induced immunosuppression exacerbates AML patients' vulnerability to life-threatening fungal infections like invasive aspergillosis (IA).
- Current diagnostic methods lack a single reliable serological marker for accurately predicting IA risk post-chemotherapy.
Purpose of the Study:
- To investigate the potential role of Glucose-6-Phosphate Dehydrogenase (G6PD) levels as a predictor of IFI risk in AML patients.
- To evaluate the correlation between serum markers such as galactomannan (GM), G6PD, and Interleukin-6 (IL-6) in AML patients with IFI.
Main Methods:
- Serum galactomannan (GM) levels were measured in AML patients during invasive aspergillosis (IA) and recovery phases.
- Serum Glucose-6-Phosphate Dehydrogenase (G6PD) levels were assessed concurrently with GM during IA and recovery.
- Interleukin-6 (IL-6) and lactate dehydrogenase (LDH) levels were measured to explore their association with fungal infection.
Main Results:
- Elevated serum GM levels were observed in AML patients during IA, decreasing upon recovery.
- Reduced serum G6PD levels were detected in AML patients during IA, with levels restoring upon recovery.
- Higher serum IL-6 levels were found during fungal infection, showing a positive correlation with LDH levels.
Conclusions:
- Monitoring serum G6PD, IL-6, and GM levels may offer a valuable approach for predicting IFI in AML patients.
- Changes in G6PD levels might be influenced by anti-cancer drugs and antibiotics, potentially impacting fungal infection risk.
- Combined monitoring of these biomarkers could improve early detection and management of IFI in immunocompromised AML patients.
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