Vasilios Kotsis

Prof. Dr. Vasilios Kotsis

orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

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

Representative Publications

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1 April 2015 in Hormones
Verified
Journal Article
Closed access
EKEvangelia Kintiraki
Evangelia Kintiraki
SPSophia Papakatsika
Sophia Papakatsika
GKGeorge Kotronis
George Kotronis
Dimitrios G. GoulisDimitrios G. Goulis
Dimitrios G. Goulis
VKVasilios Kotsis
Vasilios Kotsis
Pregnancy-induced hypertension (PIH) complicates 6-10% of pregnancies. It is defined as systolic blood pressure (SBP) >140 mmHg and diastolic blood pressure (DBP) >90 mmHg. It is classified as mild (SBP 140-149 and DBP 90-99 mmHg), moderate (SBP 150-159 and DBP 100-109 mmHg) and severe (SBP ≥ 160 and DBP ≥ 110 mmHg). PIH refers to one of four conditions: a) pre-existing hypertension, b) gestational hypertension and preeclampsia (PE), c) pre-existing hypertension plus superimposed gestational hypertension with proteinuria and d) unclassifiable hypertension. PIH is a major cause of maternal, fetal and newborn morbidity and mortality. Women with PIH are at a greater risk of abruptio placentae, cerebrovascular events, organ failure and disseminated intravascular coagulation. Fetuses of these mothers are at greater risk of intrauterine growth retardation, prematurity and intrauterine death. Ambulatory blood pressure monitoring over a period of 24 h seems to have a role in predicting deterioration from gestational hypertension to PE. Antiplatelet drugs have moderate benefits when used for prevention of PE. Treatment of PIH depends on blood pressure levels, gestational age, presence of symptoms and associated risk factors. Non-drug management is recommended when SBP ranges between 140-149 mmHg or DBP between 90-99 mmHg. Blood pressure thresholds for drug management in pregnancy vary between different health organizations. According to 2013 ESH/ESC guidelines, antihypertensive treatment is recommended in pregnancy when blood pressure levels are ≥ 150/95 mmHg. Initiation of antihypertensive treatment at values ≥ 140/90 mmHg is recommended in women with a) gestational hypertension, with or without proteinuria, b) pre-existing hypertension with the superimposition of gestational hypertension or c) hypertension with asymptomatic organ damage or symptoms at any time during pregnancy. Methyldopa is the drug of choice in pregnancy. Atenolol and metoprolol appear to be safe and effective in late pregnancy, while labetalol has an efficacy comparable to methyldopa. Angiotensin-converting enzyme (ACE) inhibitors and angiotensin II antagonists are contraindicated in pregnancy due to their association with increased risk of fetopathy.

1 October 2011 in Journal Of Hypertension
Verified
Journal Article
Closed access
VKVasilios Kotsis
Vasilios Kotsis
SSStella Stabouli
Stella Stabouli
IKIoannis Karafillis
Ioannis Karafillis
PNPeter Nilsson
Peter Nilsson
Vascular aging is described as a gradual process involving biochemical, enzymatic, and cellular changes of the vasculature and modification of the signals that modulate them. On the basis of this conception a new pathophysiological model for deeper understanding of cardiovascular risk and its treatment was introduced. The idea of early vascular aging, that is the acceleration of vascular aging seems to be a promising tool for clinical guidance in individuals at increased cardiovascular risk or a strong family history of early cardiovascular manifestations. Increased arterial stiffness, dilation of central elastic arteries, impaired endothelial function and vasodilatation are dominant aspects of this premature process.

15 December 2021 in Nutrients
Verified
Journal Article
Open access
PDF file
VKVasilios Kotsis
Vasilios Kotsis
FMFernando Martinez
Fernando Martinez
CTChristina Maria Trakatelli
Christina Maria Trakatelli
JRJosep Redon
Josep Redon
The clinical consequences of obesity on the kidneys, with or without metabolic abnormalities, involve both renal function and structures. The mechanisms linking obesity and renal damage are well understood, including several effector mechanisms with interconnected pathways. Higher prevalence of urinary albumin excretion, sub-nephrotic syndrome, nephrolithiasis, increased risk of developing CKD, and progression to ESKD have been identified as being associated with obesity and having a relevant clinical impact. Moreover, renal replacement therapy and kidney transplantation are also influenced by obesity. Losing weight is key in limiting the impact that obesity produces on the kidneys by reducing albuminuria/proteinuria, declining rate of eGFR deterioration, delaying the development of CKD and ESKD, and improving the outcome of a renal transplant. Weight reduction may also contribute to appropriate control of cardiometabolic risk factors such as hypertension, metabolic syndrome, diabetes, and dyslipidemia which may be protective not only in renal damage but also cardiovascular disease. Lifestyle changes, some drugs, and bariatric surgery have demonstrated the benefits.

1 September 2018 in Metabolism
Verified
Journal Article
Closed access
CAC. Antza
C. Antza
RCR. Cifkova
R. Cifkova
VKVasilios Kotsis
Vasilios Kotsis

1 November 2011 in Atherosclerosis
Verified
Journal Article
Closed access
VKVasilios Kotsis
Vasilios Kotsis
SSStella Stabouli
Stella Stabouli
IKIoannis Karafillis
Ioannis Karafillis
SPSofia Papakatsika
Sofia Papakatsika
ZRZoe Rizos
Zoe Rizos
PNPeter Nilsson
Peter Nilsson

1 April 2018 in Pharmacological Research
Verified
Journal Article
Closed access
CAC. Antza
C. Antza
SSS. Stabouli
S. Stabouli
VKVasilios Kotsis
Vasilios Kotsis