Anemia, Sickle Cell

"Anemia, Sickle Cell" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.

Descriptor ID	D000755
MeSH Number(s)	C15.378.071.141.150.150 C15.378.420.155 C16.320.070.150 C16.320.365.155
Concept/Terms	Anemia, Sickle Cell Anemia, Sickle Cell Anemias, Sickle Cell Sickle Cell Anemias Hemoglobin S Disease Disease, Hemoglobin S Hemoglobin S Diseases Sickle Cell Anemia Sickle Cell Disorders Cell Disorder, Sickle Cell Disorders, Sickle Sickle Cell Disorder Sickling Disorder Due to Hemoglobin S HbS Disease Sickle Cell Disease Cell Disease, Sickle Cell Diseases, Sickle Sickle Cell Diseases

Below are MeSH descriptors whose meaning is more general than "Anemia, Sickle Cell".

Diseases [C]
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Anemia [C15.378.071]
Anemia, Hemolytic [C15.378.071.141]
Anemia, Hemolytic, Congenital [C15.378.071.141.150]
Anemia, Sickle Cell [C15.378.071.141.150.150]
Hemoglobinopathies [C15.378.420]
Anemia, Sickle Cell [C15.378.420.155]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Anemia, Hemolytic, Congenital [C16.320.070]
Anemia, Sickle Cell [C16.320.070.150]
Hemoglobinopathies [C16.320.365]
Anemia, Sickle Cell [C16.320.365.155]

Below are MeSH descriptors whose meaning is related to "Anemia, Sickle Cell".

Below are MeSH descriptors whose meaning is more specific than "Anemia, Sickle Cell".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Anemia, Sickle Cell" by people in this website by year, and whether "Anemia, Sickle Cell" was a major or minor topic of these publications.

Bar chart showing 120 publications over 24 distinct years, with a maximum of 9 publications in 2014

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1995	1	0	1
1997	2	1	3
2001	2	0	2
2003	1	0	1
2004	2	0	2
2005	3	1	4
2006	7	0	7
2007	7	0	7
2008	8	0	8
2009	7	1	8
2010	3	0	3
2011	7	0	7
2012	7	1	8
2013	3	0	3
2014	9	0	9
2015	6	0	6
2016	5	1	6
2017	4	0	4
2018	7	0	7
2019	1	0	1
2020	7	1	8
2021	4	0	4
2022	3	0	3
2023	8	0	8

Below are the most recent publications written about "Anemia, Sickle Cell" by people in Profiles.

Bashi A, Lekpor C, Hood JL, Thompson WE, Stiles JK, Driss A. Modulation of Heme-Induced Inflammation Using MicroRNA-Loaded Liposomes: Implications for Hemolytic Disorders Such as Malaria and Sickle Cell Disease. Int J Mol Sci. 2023 Nov 29; 24(23).

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Adamkiewicz TV, Yee MEM, Thomas S, Tunali A, Lai KW, Omole FS, Lane PA, Yildirim I. Pneumococcal infections in children with sickle cell disease before and after pneumococcal conjugate vaccines. Blood Adv. 2023 11 14; 7(21):6751-6761.

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Zhang X, Song J, Shah BN, Han J, Hassan T, Miasniakova G, Sergueeva A, Nekhai S, Machado RF, Gladwin MT, Saraf SL, Prchal JT, Gordeuk VR. Gene expression changes in sickle cell reticulocytes and their clinical associations. Sci Rep. 2023 08 08; 13(1):12864.

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Ahmad A, Kumari N, Afangbedji N, Nekhai S, Jerebtsova M. Induction of Hepcidin Expression in the Renal Cortex of Sickle Cell Disease Mice. Int J Mol Sci. 2023 Jun 28; 24(13).

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Castro-Sesquen YE, Saraf SL, Gordeuk VR, Nekhai S, Jerebtsova M. Use of multiple urinary biomarkers for the early detection of chronic kidney disease in sickle cell anemia. Blood Adv. 2023 06 13; 7(11):2606-2608.

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Oxendine Harp K, Bashi A, Botchway F, Addo-Gyan D, Tetteh-Tsifoanya M, Lamptey A, Djameh G, Iqbal SA, Lekpor C, Banerjee S, Wilson MD, Dei-Adomakoh Y, Adjei AA, Stiles JK, Driss A. Sickle Cell Hemoglobin Genotypes Affect Malaria Parasite Growth and Correlate with Exosomal miR-451a and let-7i-5p Levels. Int J Mol Sci. 2023 Apr 19; 24(8).

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Dampier CD, Telen MJ, Wun T, Brown RC, Desai P, El Rassi F, Fuh B, Kanter J, Pastore Y, Rothman J, Taylor JG, Readett D, Sivamurthy KM, Tammara B, Tseng LJ, Lozier JN, Thackray H, Magnani JL, Hassell KL. A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis. Blood. 2023 01 12; 141(2):168-179.

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Earley EJ, Kelly S, Fang F, Alencar CS, Rodrigues DOW, Soares Cruz DT, Flanagan JM, Ware RE, Zhang X, Gordeuk V, Gladwin M, Zhang Y, Nouraie M, Nekhai S, Sabino E, Custer B, Dinardo C, Page GP. Genome-wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci. Br J Haematol. 2023 04; 201(2):343-352.

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Chambliss C, Stiles JK, Gee BE. Neuregulin-1 attenuates hemolysis- and ischemia induced-cerebrovascular inflammation associated with sickle cell disease. J Stroke Cerebrovasc Dis. 2023 Feb; 32(2):106912.

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Valle J, Baker JR, Madrigal D, Ferrerosa J, Paulukonis S. Sickle cell disease among Latinx in California. PLoS One. 2022; 17(10):e0276653.

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