Saarah Davids

Dr. Saarah Davids

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 May 2021 in Diagnostics
Verified
Journal Article
Open access
PDF file
CWCecil Jack Weale
Cecil Jack Weale
DMDon Matshazi
Don Matshazi
SDSaarah Davids
Saarah Davids
Shanel RaghubeerShanel Raghubeer
Shanel Raghubeer
RERajiv Erasmus
Rajiv Erasmus
TMTandi E Matsha
Tandi E Matsha
This cross-sectional study investigated the association of miR-1299, -126-3p and -30e-3p with and their diagnostic capability for dysglycaemia in 1273 (men, n = 345) South Africans, aged >20 years. Glycaemic status was assessed by oral glucose tolerance test (OGTT). Whole blood microRNA (miRNA) expressions were assessed using TaqMan-based reverse transcription quantitative-PCR (RT-qPCR). Receiver operating characteristic (ROC) curves assessed the ability of each miRNA to discriminate dysglycaemia, while multivariable logistic regression analyses linked expression with dysglycaemia. In all, 207 (16.2%) and 94 (7.4%) participants had prediabetes and type 2 diabetes mellitus (T2DM), respectively. All three miRNAs were significantly highly expressed in individuals with prediabetes compared to normotolerant patients, p < 0.001. miR-30e-3p and miR-126-3p were also significantly more expressed in T2DM versus normotolerant patients, p < 0.001. In multivariable logistic regressions, the three miRNAs were consistently and continuously associated with prediabetes, while only miR-126-3p was associated with T2DM. The ROC analysis indicated all three miRNAs had a significant overall predictive ability to diagnose prediabetes, diabetes and the combination of both (dysglycaemia), with the area under the receiver operating characteristic curve (AUC) being significantly higher for miR-126-3p in prediabetes. For prediabetes diagnosis, miR-126-3p (AUC = 0.760) outperformed HbA1c (AUC = 0.695), p = 0.042. These results suggest that miR-1299, -126-3p and -30e-3p are associated with prediabetes, and measuring miR-126-3p could potentially contribute to diabetes risk screening strategies.

20 December 2022 in Biomedicines
Verified
Journal Article
Open access
PDF file
YPYvonne Prince
Yvonne Prince
GDGlenda Mary Davison
Glenda Mary Davison
SDSaarah Davids
Saarah Davids
RERajiv Erasmus
Rajiv Erasmus
AKAndre Pascal Kengne
Andre Pascal Kengne
TMTandi E Matsha
Tandi E Matsha
The oral microbiota plays a crucial role in both systemic inflammation and metabolic syndrome (MetS), which is characterised by low-grade inflammation. Studies have analysed the gut microbiota using stool specimens from subjects with MetS; however, the etiological role of the oral microbiota in the development of MetS is still uncertain. We investigated the oral microbiota of 128 subgingival plaque samples from a South African cohort with and without MetS. After a comprehensive analysis of the oral microbiota, we observed a significant increase in Gram-positive aerobic and anaerobic microbiota in those with MetS. We observed an abundance of Actinomyces, Corynebacterium, and Fusobacterium genera in the MetS group, which differed significantly from previous studies, which found Granulicatella to be enriched in MetS. To further assess the impact of the metabolic parameters (FBG, Waist C, HDL, TGs, and BP) on the oral microbiota, we calculated the odds ratio (ORs) for significant oral microbiota identified between the MetS groups. We found that different species were associated with at least four MetS risk factors. This study has shown that the oral microbiota is disrupted in MetS and may promote inflammation providing a gateway to other systemic diseases, including diabetes and cardiovascular diseases.

30 July 2022 in Nutrients
Verified
Journal Article
Open access
PDF file
RERajiv Erasmus
Rajiv Erasmus
SMSetjie Maepa
Setjie Maepa
IMIan Machingura
Ian Machingura
SDSaarah Davids
Saarah Davids
Shanel RaghubeerShanel Raghubeer
Shanel Raghubeer
TMTandi E Matsha
Tandi E Matsha
Vitamin D reportedly plays an important role in the pathogenesis of diabetes mellitus; however, this role is unclear and debated. This study investigated the association between 25(OH) vitamin D, vitamin D-binding proteins, and vitamin D receptor (VDR) polymorphisms in healthy individuals and those with prediabetes and type 2 diabetes mellitus (T2D) from South Africa. A cross-sectional study was conducted involving subjects of mixed ancestry aged ≥20 years. Males presented with higher mean 25(OH) vitamin D levels than females, while females exhibited significantly higher serum vitamin D-binding protein levels. Significant differences in mean 25(OH) vitamin D levels were observed in normo-glycaemic, prediabetes, screen-detected DM, and known DM individuals. Vitamin D receptor SNPs Fok1 and Taq1 were not associated with glycaemic status. Fok1 was not associated with 25(OH) vitamin D deficiency, while Taq1 was associated with vitamin D insufficiency. This study showed a high prevalence of vitamin D deficiency/insufficiency in this South African population, with decreased vitamin D levels observed in hyperglycaemic individuals, which was not linked to either vitamin D-binding protein or polymorphisms in Fok1 of the VDR gene. These results may be used as a platform for further research into diagnosis and treatment of hyperglycaemia.

28 June 2019 in South African Medical Journal
Verified
Journal Article
Open access
PDF file
SDSaarah Davids
Saarah Davids
TMT E Matsha
T E Matsha
NPN Peer
N Peer
RER T Erasmus
R T Erasmus
AKAndre Pascal Kengne
Andre Pascal Kengne
Increase in blood pressure over a 7-year period in a mixed-ancestry South African population

1 October 2014 in Behavioural Brain Research
Verified
Journal Article
Closed access
MKM. Kinder
M. Kinder
MLMartin Lotze
Martin Lotze
SDSaarah Davids
Saarah Davids
MDM. Domin
M. Domin
KTK. Thoms
K. Thoms
HLH. Lauffer
H. Lauffer

5 January 2023 in African Journal of Laboratory Medicine
Verified
Journal Article
Open access
JRJason Van Rensburg
Jason Van Rensburg
SDSaarah Davids
Saarah Davids
CSCarine Smuts
Carine Smuts
GDGlenda Mary Davison
Glenda Mary Davison
Background: Sepsis is characterised by multi-organ failure due to an uncontrolled immune response to infection. Sepsis prevalence is increased in developing countries and requires prompt diagnosis and treatment. Reports, although controversial, suggest that full blood count parameters and cell ratios could assist in the early screening for sepsis.Objective: The study evaluated the use of haematological cell ratios in screening for sepsis in a South African population.Methods: The study retrospectively analysed the complete blood counts, blood cultures (BC) and biochemical test results of 125 adult patients who presented between January 2021 and July 2021 at a hospital in Cape Town. An ISO15189-accredited laboratory performed all of the tests. We compared and correlated the automated differential counts, neutrophil, monocyte and platelet-to-lymphocyte ratios with procalcitonin levels. A p-value of 0.05 was considered significant.Results: Sixty-two sepsis patients (procalcitonin 2 ng/L and positive BC) were identified and compared to 63 non-sepsis controls. All cell ratios were significantly elevated in sepsis patients (p 0.001). However, the two groups had no significant difference in absolute monocyte counts (p = 0.377). In addition, no correlation was detected between any cell ratios and procalcitonin.Conclusion: In combination with complete blood count parameters, haematology cell ratios can be used for early sepsis detection. The full blood count is widely available, inexpensive, and routinely requested by emergency care clinicians. Although procalcitonin and BC remain the gold standard, the calculation of cell ratios could provide a simple screening tool for the early detection of sepsis.What this study adds: This study adds evidence to the proposal that calculating haematological cell ratios assists in the early screening of sepsis in a South African setting.