Evidence map›Paper›PMID 40609076›Full record

ArticleBlood advances2025

Sex and genotype specificities of microvasculature and muscle remodeling in sub-Saharan sickle cell trait and disease.

Léo Blervaque, Pablo Bartolucci, Manon Riccetti, Marion Ravelojaona, Angèle N Merlet, Mathilde Noguer, Manon Rojo, Christophe Hourdé, Cyril Martin, Vincent Pialoux and 5 more

Abstract read
In one paragraph

Article in Blood advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Léo BlervaqueLaboratoire Interuniversitaire de Biologie de la Motricité, Université Savoie Mont Blanc, Chambéry, France.ORCID 0000-0003-0616-1908
Pablo BartolucciSickle Cell Referral Center, Department of Internal Medicine at Henri-Mondor University Hospital, Université Paris-Est Créteil, Assistance Publique-Hôpitaux de ParisAP-HP, Créteil, France.ORCID 0000-0002-7007-1344
Manon RiccettiLaboratoire Interuniversitaire de Biologie de la Motricité, Université Savoie Mont Blanc, Chambéry, France.ORCID 0000-0003-4806-9034
Marion RavelojaonaUnité de Myologie-Service de Physiologie Clinique et de l'Exercice, Centre Hospitalier Universitaire Saint-Etienne, Laboratoire Interuniversitaire de Biologie de la Motricité, Université Jean Monnet Saint-Etienne, Saint-Etienne, France.
Angèle N MerletUnité de Myologie-Service de Physiologie Clinique et de l'Exercice, Centre Hospitalier Universitaire Saint-Etienne, Laboratoire Interuniversitaire de Biologie de la Motricité, Université Jean Monnet Saint-Etienne, Saint-Etienne, France.ORCID 0000-0002-7597-119X
Mathilde NoguerLaboratoire Interuniversitaire de Biologie de la Motricité, Université Savoie Mont Blanc, Chambéry, France.ORCID 0009-0000-0621-5940
Manon RojoLaboratoire Interuniversitaire de Biologie de la Motricité, Université Savoie Mont Blanc, Chambéry, France.
Christophe HourdéLaboratoire Interuniversitaire de Biologie de la Motricité, Université Savoie Mont Blanc, Chambéry, France.ORCID 0000-0001-5209-2590
Cyril MartinLaboratoire Interuniversitaire de Biologie de la Motricité, Université Claude Bernard Lyon 1, Université de Lyon, Villeurbanne, France.
Vincent PialouxLaboratoire Interuniversitaire de Biologie de la Motricité, Université Claude Bernard Lyon 1, Université de Lyon, Villeurbanne, France.
Barnabas GellenPolyclinique de Poitiers, ELSAN, Poitiers, France.ORCID 0000-0002-1128-2985
Frédéric GalactérosSickle Cell Referral Center, Department of Internal Medicine at Henri-Mondor University Hospital, Université Paris-Est Créteil, Assistance Publique-Hôpitaux de ParisAP-HP, Créteil, France.ORCID 0000-0001-8130-1208
Samuel Oyono-EnguélléLaboratoire de Physiologie, Faculté de médecine, Université Yaoundé 1, Yaoundé, Cameroon.
Léonard FéassonUnité de Myologie-Service de Physiologie Clinique et de l'Exercice, Centre Hospitalier Universitaire Saint-Etienne, Laboratoire Interuniversitaire de Biologie de la Motricité, Université Jean Monnet Saint-Etienne, Saint-Etienne, France.ORCID 0000-0002-8163-5539
Laurent A MessonnierLaboratoire Interuniversitaire de Biologie de la Motricité, Université Savoie Mont Blanc, Chambéry, France.ORCID 0000-0001-8823-1986

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractSickle cell disease (SCD) is associated with microvascular and muscle remodeling as well as reduced exercise tolerance. However, SCD repercussions on microvasculature and muscle in women remain unknown. This study aimed to compare (1) muscle microvascular and energetic characteristics of female and male healthy individuals (CON), carriers of sickle cell trait (SCT), and patients with SCD; and (2) adaptations to endurance training (ET) compared with habitual life (untrained [UT]) in patients. In SCD, correlations between capillary density and plasma L-selectin and intercellular adhesion molecule and between capillary diameter and mean corpuscular hemoglobin S concentration were noticed (P < .01 all). The capillary network rarefaction observed in SCD was more pronounced in women than in men (interaction: P < .01). Muscle hypoxia markers were not different between groups. Compared with CON, the surface area for 100 myocytes was lower in men with SCD (both P < .001) but not in women. Advanced oxidation protein products were increased in patients with SCD and to a greater extent in men (interaction: P < .02). Components of muscle pH regulation were specifically higher in SCT. Compared with UT, ET saw its microvascular network and oxidative capacities increase, without differences between men and women. Our results suggest that SCD-associated capillary rarefaction and enlargement could be related to disturbed hemodynamics and reduced erythrocytes deformability, respectively. The specific remodeling in female patients with SCD included aggravated microvascular remodeling but preserved myocytes. Muscle pH regulation mechanisms appeared specifically upregulated in carriers of SCT. Men and women with SCD improved similarly their microvasculature and muscle energetic characteristics in response to ET.

Indexed as

GenotypeMicrovesselsMuscle, SkeletalSickle Cell TraitAdultFemaleHumansMaleSex FactorsYoung Adult

Identifiers

PMID40609076
PMCPMC12496247

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