Myocardial Ischemia in Patients with Sickle Cell Disease: A Retrospective Review

Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 2189-2189
Author(s):  
Payal C. Desai ◽  
Nicole Kendel ◽  
Spero R Cataland ◽  
Eric H. Kraut ◽  
Ying Huang ◽  
...  

Abstract Introduction: On an autopsy study of 306 patients with sickle cell disease (SCD), cardiovascular disease is observed in 58% of patients and myocardial microinfarcts were noted in 20% of patients. Previously data from our center indicates that approximately 13% (3/22) patients demonstrated cardiac microvascular disease in steady state. However, the incidence of myocardial ischemic injury in patients with SCD presenting with chest pain remains largely undefined. Methods: We conducted a single institution retrospective chart review from September 2009 through September 2014 to evaluate the incidence of elevated troponin-I (normal < 0.11ng/ml), which is a well-established biomarker of myocardial injury, in patients with SCD and chest pain. We further characterize each of these episodes with cardiac magnetic resonance imaging, if available, and clinical and laboratory findings at the time of the event. Kruskal-Wallis test was used to compare troponin measurement values among different groups of patients. Results: A total of 25 (10 female, 15 male) of the 352 (7%) of patients followed at the Ohio State Comprehensive Sickle Cell Center had troponin elevation over a 5 year period. They had a total of thirty-eight individual encounters with troponin elevations (range: 0.11-12.17) [72% patients with 1 elevation, 28% patients multiple troponin elevations) (range: 1-4 incidences)]. The median age at the time of troponin elevation was 36 (Range: 20.5-66 yrs). Troponin elevation was observed in patients of all genotypes (76% SS; 4% SBeta+; 20% SC). 6/25 (25%) of patients with troponin elevation in the past five years are now deceased. Thirteen patients (52%) had acute chest syndrome and ten patients (40%) had acute kidney injury at the time of troponin elevation. The degree of troponin elevation was not associated with concurrent acute chest syndrome, concurrent acute kidney injury or mortality. At the encounter level, median troponin at diagnosis was 0.3 (range: 0.11-12.2) and the median peak troponin was 0.4 (range: 0.11-38.1),. The median value of TR jet velocity at baseline was 2.8 (range: 1.1-3.7) (n=23) and the median TR jet velocity at the time of elevation was 3.0 (range: 1.7-4.6) (n=28). Median baseline hemoglobin was 8 (range: 4.5-12.6) and median hemoglobin at encounter was 7.5 (range: 4.3-12.5), resulting in a median change in hemoglobin of -0.4 (range: -6.2 - 2.5). Four of 10 MRI obtained at the time of troponin elevation showed myocardial ischemia and 3/10 patients showed late gadolinium enhancement indicating myocardial injury. Conclusion: Patients with SCD presenting with chest pain have myocardial ischemia and infarctions as demonstrated in our population by both troponin elevation and cardiac imaging. While, the long term implications of this finding are currently being studied in a multi-centered prospective study, further cardiac evaluations should be considered in patients with SCD presenting with chest pain. Disclosures Desai: Pfizer: Consultancy. Cataland:Ablynx: Consultancy. Raman:Siemens: Consultancy.

Blood ◽  
2019 ◽  
Vol 134 (Supplement_1) ◽  
pp. 78-78
Author(s):  
Samit Ghosh ◽  
Oluwaseun Orikogbo ◽  
Rimi Hazra ◽  
Bethany Flage ◽  
Danielle Crosby ◽  
...  

Acute kidney injury (AKI) is a major clinical concern during episodes of acute chest syndrome and vaso-occlusive crisis in sickle cell disease (SCD). AKI increases the risk of chronic kidney disease (CKD) and end stage renal disease (ESRD). We previously showed that alpha-1-microglobulin (A1M), a low affinity heme-binding protein that carries heme for renal clearance is elevated in patients and mice with homozygous SCD (SS). Hemopexin (Hx), which primarily scavenges circulating heme to the liver, is exhausted in SCD. In this study, we explored the idea that acquired Hx deficiency in SCD is a risk factor for AKI development in SCD. We studied mice with a global knockout of Hx with no detectable plasma Hx at baseline. Plasma A1M was significantly elevated in the Hx-/-mice compared to control (Hx+/+) mice (n=5; p&lt;0.01). We then transplanted whole bone marrow cells from SS mice into Hx+/+and Hx-/-mice to create bone marrow chimeric SSHx+/+and SSHx-/-mice with SCD phenotype. The chimeras had elevated plasma A1M compared to recipient littermates (Hx+/+and Hx-/-) and low baseline glomerular filtration rate (GFR). Modest elevation of circulating heme with infusion of hemin (20 μmoles/kg bw) worsened GFR and caused severe AKI. Next, to determine whether hemin induced AKI is attenuated by elevation of circulating Hx, we infused SS mice with purified Hx, and control SS mice with either purified A1M or vehicle immediately prior to the hemin challenge. We observed improved GFR in the Hx-treated SS mice, while vehicle and A1M-treated mice suffered 23% and 39% loss of GFR respectively compared to their baseline. In agreement with the GFR data, the levels of several AKI diagnostic markers, plasma creatinine (plasma Cr), urinary albumin-creatinine ratio (uACR) and kidney injury molecule (uKIM-1) were elevated significantly in vehicle and A1M treated mice following hemin challenge. In Hx-treated mice, these biomarkers remained unaltered. Importantly, Hx infusions re-directed excess heme in SS mice to the liver, while A1M infusion significantly increased total heme content in the kidneys. Two-way ANOVA analysis of GFR (p&lt;0.01) and plasma Cr (p&lt;0.001) revealed significant exacerbation of kidney injury in A1M treated SS mice compared to vehicle treated mice. Histopathology of renal tissue showed considerable tissue damage in vehicle and A1M infused SS mice, while Hx treated SS mice kidneys appeared relatively normal. This study provides genetic evidence that hemopexin deficiency promotes AKI development in SCD, and we provide proof-of-principle for hemopexin replacement therapy to treat AKI in SCD. Disclosures Ofori-Acquah: Shire Human Genetic Therapies Inc: Other: Financial Relationship.


Blood ◽  
2020 ◽  
Author(s):  
Solomon Ofori-Acquah ◽  
Rimi Hazra ◽  
Oluwaseun O Orikogbo ◽  
Danielle Crosby ◽  
Bethany Flage ◽  
...  

Acute kidney injury (AKI) is a major clinical concern in sickle cell disease (SCD). Clinical evidence suggests that red cell alarmins may cause AKI in SCD however the sterile inflammatory process involved has hitherto not been defined. We discovered that hemopexin deficiency in SCD is associated with a compensatory increase in alpha-1-microglobulin (A1M) resulting in up to 10-fold higher A1M/hemopexin ratio in SCD compared to health controls. The A1M/hemopexin ratio is associated with markers of hemolysis and AKI in both humans and mice with SCD. Studies in mice showed that excess heme is directed to the kidneys in SCD in a process involving A1M causing AKI while excess heme in controls is transported to the liver as expected. Using genetic and bone marrow chimeric tools, we confirmed that hemopexin deficiency promotes AKI in sickle mice under hemolytic stress. However, AKI was blocked when hemopexin deficiency in sickle mice was corrected with infusions of purified hemopexin prior to the induction of hemolytic stress. This study identifies acquired hemopexin deficiency as a risk factor of AKI in SCD and hemopexin replacement as a potential therapy.


2018 ◽  
Vol 93 (8) ◽  
pp. E198-E200 ◽  
Author(s):  
Jamie Oakley ◽  
Rima Zahr ◽  
Inmaculada Aban ◽  
Varsha Kulkarni ◽  
Rakesh P. Patel ◽  
...  

2017 ◽  
Vol 32 (8) ◽  
pp. 1287-1291 ◽  
Author(s):  
Cherry Mammen ◽  
Mei Lin Bissonnette ◽  
Douglas G. Matsell

2018 ◽  
Vol 10 (1) ◽  
pp. 2018032 ◽  
Author(s):  
Kwame Ofori Adjepong ◽  
Folashade Otegbeye ◽  
Yaw Amoateng ADJEPONG

An estimated 30 million people worldwide have sickle cell disease (SCD).  Emergent and non-emergent surgical procedures in SCD have been associated with relatively increased risks of peri-operative mortality, vaso-occlussive (painful) crisis, acute chest syndrome, post-operative infections, congestive heart failure, cerebrovascular accident and acute kidney injury.  Pre-operative assessment must include careful review of the patient’s known crisis triggers, baseline hematologic profile, usual transfusion requirements, pre-existing organ dysfunction and narcotic use. Use of preoperative blood transfusions should be selective and decisions individualized based on the baseline hemoglobin, surgical procedure and anticipated volume of blood loss.  Intra- and post-operative management should focus on minimizing hypoxia, hypothermia, acidosis, and intravascular volume depletion. Pre- and post-operative incentive spirometry use should be encouraged. 


2020 ◽  
Vol 189 (3) ◽  
pp. 559-565
Author(s):  
Meghan McCormick ◽  
Troy Richardson ◽  
Bradley A. Warady ◽  
Enrico M. Novelli ◽  
Ramasubramanian Kalpatthi

Author(s):  
Soi Avgeridou ◽  
Ilija Djordjevic ◽  
Anton Sabashnikov ◽  
Kaveh Eghbalzadeh ◽  
Laura Suhr ◽  
...  

AbstractExtracorporeal membrane oxygenation (ECMO) plays an important role as a life-saving tool for patients with therapy-refractory cardio-respiratory failure. Especially, for rare and infrequent indications, scientific data is scarce. The conducted paper focuses primarily on our institutional experience with a 19-year-old patient suffering an acute chest syndrome, a pathognomonic pulmonary condition presented by patients with sickle cell disease. After implementation of awake ECMO therapy, the patient was successfully weaned off support and discharged home 22 days after initiation of the extracorporeal circulation. In addition to limited data and current literature, further and larger data sets are necessary to determine the outcome after ECMO therapy for this rare indication.


Toxins ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 157
Author(s):  
Joyce Gonzales ◽  
Trinad Chakraborty ◽  
Maritza Romero ◽  
Mobarak Abu Mraheil ◽  
Abdullah Kutlar ◽  
...  

Sickle cell disease (SCD) is one of the most common autosomal recessive disorders in the world. Due to functional asplenia, a dysfunctional antibody response, antibiotic drug resistance and poor response to immunization, SCD patients have impaired immunity. A leading cause of hospitalization and death in SCD patients is the acute chest syndrome (ACS). This complication is especially manifested upon infection of SCD patients with Streptococcus pneumoniae (Spn)—a facultative anaerobic Gram-positive bacterium that causes lower respiratory tract infections. Spn has developed increased rates of antibiotics resistance and is particularly virulent in SCD patients. The primary defense against Spn is the generation of reactive oxygen species (ROS) during the oxidative burst of neutrophils and macrophages. Paradoxically, Spn itself produces high levels of the ROS hydrogen peroxide (H2O2) as a virulence strategy. Apart from H2O2, Spn also secretes another virulence factor, i.e., the pore-forming exotoxin pneumolysin (PLY), a potent mediator of lung injury in patients with pneumonia in general and particularly in those with SCD. PLY is released early on in infection either by autolysis or bacterial lysis following the treatment with antibiotics and has a broad range of biological activities. This review will discuss recent findings on the role of pneumococci in ACS pathogenesis and on strategies to counteract the devastating effects of its virulence factors on the lungs in SCD patients.


2021 ◽  
pp. 1-5
Author(s):  
Justin E. Juskewitch ◽  
Craig D. Tauscher ◽  
Sheila K. Moldenhauer ◽  
Jennifer E. Schieber ◽  
Eapen K. Jacob ◽  
...  

Introduction: Patients with sickle cell disease (SCD) have repeated episodes of red blood cell (RBC) sickling and microvascular occlusion that manifest as pain crises, acute chest syndrome, and chronic hemolysis. These clinical sequelae usually increase during pregnancy. Given the racial distribution of SCD, patients with SCD are also more likely to have rarer RBC antigen genotypes than RBC donor populations. We present the management and clinical outcome of a 21-year-old pregnant woman with SCD and an RHD*39 (RhD[S103P], G-negative) variant. Case Presentation: Ms. S is B positive with a reported history of anti-D, anti-C, and anti-E alloantibodies (anti-G testing unknown). Genetic testing revealed both an RHD*39 and homozygous partial RHCE*ceVS.02 genotype. Absorption/elution testing confirmed the presence of anti-G, anti-C, and anti-E alloantibodies but could not definitively determine the presence/absence of an anti-D alloantibody. Ms. S desired to undergo elective pregnancy termination and the need for postprocedural RhD immunoglobulin (RhIG) was posed. Given that only the G antigen site is changed in an RHD*39 genotype and the potential risk of RhIG triggering a hyperhemolytic episode in an SCD patient, RhIG was not administered. There were no procedural complications. Follow-up testing at 10 weeks showed no increase in RBC alloantibody strength. Discussion/Conclusion: Ms. S represents a rare RHD*39 and partial RHCE*ceVS.02 genotype which did not further alloimmunize in the absence of RhIG administration. Her case also highlights the importance of routine anti-G alloantibody testing in women of childbearing age with apparent anti-D and anti-C alloantibodies.


1995 ◽  
Vol 62 (2) ◽  
pp. 201-205 ◽  
Author(s):  
H. A. Srair ◽  
J. A. Owa ◽  
H. A. Aman ◽  
M. A. Madan

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