GENETIC TESTING FOR THROMBOPHILIA IN CASE OF UNPROVOKED EPISODE OF PULMONARY EMBOLISM Текст научной статьи по специальности «Клиническая медицина»

ВИПАДОК13 ПРАКТИКИ

UDC 616.2-005.6/.7-074:616.151.5:57.088.7 https://doi.Org/10.26641/2307-0404.2021.2.234734

T.V. Kirieieva, GENETIC TESTING FOR THROMBOPHILIA

TA. Pertseva, ш CASE OF UNPROVOKED EPISODE

NK Kravchenko' OF PULMONARY EMBOLISM

B.O. Basina

Dnipro State Medical University

department of internal medicine 1

V. Vernadsky str., 9, Dnipro, 49044, Ukraine

Днтровський державний медичний утверситет

кафедра внутрiшньоi медицини 1

(зав. - д. мед. н. проф. Л.1. Конопкта)

вул. В. Вернадського, 9, Днтро, 49044, Украта1ГУ

e-mail: simmetrichno@gmail.com

Цитування: Медичт перспективы. 2021. Т. 26, № 2. С. 197-201 Cited: Medicniperspektivi. 2021;26(2):197-201

Key words: pulmonary embolism, thrombophilia, low risk patient Ключовi слова: ТЕЛА, тромбофiлiя, пащент низького ризику Ключевые слова: ТЭЛА, тромбофилия, пациент низкого риска

Abstract. Genetic testing for thrombophilia in case of unprovoked episode of pulmonary embolism. Kirieieva T.V., Pertseva T.A., Kravchenko N.K., Basina B.O. Venous thromboembolism (pulmonary embolism (PE) and deep vein thrombosis (DVT)) is the third among all cardiovascular syndromes in the world, second only to heart attack and stroke. Estimation of clinical probability of this condition takes into account many factors, including age. But in case of PE probability in young patient data of scales such as Geneva Score (Revised), Wells' criteria for pulmonary embolism, the PERC rule may be misleading. For this group a new influential factor emerges -thrombophilia. The aim of our work was to demonstrate the approach to identifying whom and when to test for genetic predisposition for thrombosis, based on a clinical case of young male with unprovoked episode of PE. Testing patients for thrombophilia is a good way to develop a personalised approach in case of prescribing long-term anticoagulant treatment. Moreover, patient's awareness about congenital condition helps to increase complience which is crucial, due to the fact that in case of unprovoked pulmonary embolism another episode can occur in up to 50 % of cases during the next 5 years. In addition, further accumulation and analysis of data on the amount ofgenetic risk factors for thrombosis will expand our understanding of this issue and in the future will allow us to better diagnose and treat this condition.

Реферат. Генетичне тестування на тромбофШю в pa3i неспровокованого ешзоду ТЕЛА. Юреева Т.В., Перцева Т.О., Кравченко Н.К., Басша Б.О. Венозт тромбоемболп (тромбоемболiя легеневог артерп (ТЕЛА) i тромбоз глибоких вен (ТГВ)) в усьому свimi поадають трете мкце серед ycix кардюваскулярних синдромiв, поступаючись тшьки тфаркту та тсульту. Оцiнка клШчно! ймовiрностi цього стану враховуе безлiч факторiв, у тому числi вк Однак при оцiнцi ймовiрностi ТЕЛА в молодих пацiентiв без значущих чинниюв ризику за допомогою основних шкал, таких як r Geneva Score (Revised), Wells 'Criteria for Pulmonary Embolism, правилу PERC, отриманий результат може не вiдповiдати клiнiчнiй картит. Для таких хворих зростае роль наявностi генетичног схильностi до тромбоутворення - тромбофши. Метою нашог роботи було на прикладi клтчного випадку продемонструвати мкце тестування на тромбофШю в планi ведення молодого хворого з неспровокованим еп1зодом ТЕЛА. Тестування пацiентiв на тромбофШю допомагае у розробц персона-лiзованого пiдходу в разi необхiдностi призначення тривалог терапИ антикоагулянтами. Крiм того, обiзна-нiсть пацiента щодо своег генетичног схильностi допомагае пiдвищити комплаенттсть, що вкрай важливо з огляду на високий ризик повторних епiзодiв тромбозу в наступт п 'ять роюв. Крiм того, подальше накопичення i аналiз даних про сукуптсть генетичних факторiв ризику тромбозу розширить наше розумiння цiеi проблеми i в майбутньому дозволить нам краще дiагностувати та л^вати цей стан.

Venous thromboembolism (pulmonary embolism (PE) and deep vein thrombosis (DVT)) is the third among all cardiovascular syndromes in the world, second only to heart attack and stroke [9, 10]. PE is one of the most formidable complications developing in postoperative patients and patients with lower limb vascular thrombosis.

Nowadays, in clinical practice we have tools which help us to objectify the risk of PE development in order to either timely prevent or treat it. The risk of PE is determined by the Geneva Score (Revised), Wells' Criteria for Pulmonary Embolism, the PERC rule. They all take into account risk factors such as age (>65 years old Geneva Score and

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>50 years old PERC), prolonged immobilization, surgical intervention and history of DVT [11, 6]. However, in clinical practice, cases of PE development in young patients without the so-called "strong provoking factors" are rather common. In this cases a new factor emerges - genetic predisposition known as thrombophilia. This term means an increased tendency to thrombosis developing as a result of genetic or acquired changes in the haemostatic system [8, 9].

In routine clinical practice, detection of throm-bophilia is most commonly used in management of pregnancy and the postpartum period [4]. The role of genetic predisposition is also considered when planning surgical interventions so as to predict the need for the prevention of thrombosis in the postoperative period. For this, the Caprini scale is used (mutations of factor V (Leiden) and the prothrombin gene is taken into account). In case of hospitalized non-surgical patients, the need for thrombopro-phylaxis is determined by the PADUA score in which the presence of a previously diagnosed throm-bophlic condition is also considered. However, in the diagnosis and further management of patients with pulmonary embolism, the role of thrombophilia markers is not unambiguous [7].

In majority of cases, detection of this condition in patients with PE is the final stage of the diagnostic search, after all provoking factors have been excluded. Only in case of an "unprovoked" PE it makes sense to think about conducting tests for thrombo-philia. Currently, there is no unequivocal approach to decide whom and when to test. For example, the British committee for standards in haematology, 2010 in its recommendations states that it is not

possible to give valid recommendations regarding testing of patients and their families [1]. Recently, a number of publications systematized the approach to this issue. Scott M. Stevens et al., 2016, based on a meta-analysis of large studies, concluded that testing for a genetic predisposition in patients with unprovoked thrombosis is not worth, except for cases when presence of thrombophilia gene can increase patient's adherence to anticoagulant therapy [3]. On the other hand all publications emphasize that this field continues to develop. Moreover, all current studies considered only factors strongly associated with the risk of thrombosis (antithrombin (AT), protein C (PC) and protein S (PS) factor V Leiden (FVL) and the prothrombin gene 20 210 A / G (PGM) mutations), while other factors currently available for determination ((PAI-1), and the 4G / 5G PAI-1 promoter polymorphism, folate cycle mutations MTHFR 677 and MTRR 66) and their combinations were not taken into account [2].

The aim of our work was to show, the role of testing for thrombophilia in young patients without "major risk factors" of PE basing on the clinical case.

A 36-year-old male was admitted to the hospital with complains on dyspnea left sided chest pain, fever 37,7°C, SpO2 94 %. Prior to this he has been ill for 3 days, the onset was acute, initial symptoms were chest pain and fever and mild dyspnea on exertion. Chest X-ray showed left-sided pleural effusion and a diagnose of CAP was established (Fig. 1). Pleural fluid analysis showed exudate and patient was given the standard antibacterial therapy (amoxicillin+clavulanic acid 1.2 g iv t.i.d. and azythromicine 500 mg per os q.d.).

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Fig. 1. Frontal chest X-ray on the day of admission

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On day three he showed no clinical improvement with multiple isolated effusions in paracostal and a CT scan of chest was performed. It showed (52 mm), supraphrenic (32 mm), and interlobar partial atelectasis of the lower lobe of the left lung (31 mm) areas (Fig. 2).

Fig. 2. Chest CT on day three of treatment

Due to the fact that clinical signs of the disease differed from the typical clinic of pneumonia: absence of leukocytosis, low CRP (16.8 mg/l), the absence of purulent sputum and limited pleural effusion, the diagnosis of CAP was considered as unlikely, unfortunately pneumonia is still often misdiagnosed [5]. In addition, guided by the ultrasound another thoracocentesis was performed in order to check the fluid for presence of myco-bacterium and other bacterium. PCR for all

pathogens were negative. In a detailed medical history, patient mentioned that a few days before the onset of the disease, he was on a business trip and spent more than three hours on the road. This fact, in combination with the clinical picture atypical for pneumonia, made it possible to suspect PE.

First of all we considered a pre-test probability of this diagnosis. Judging by Wells scale the probability of PE was 0 points, rGeneva - 3 points (due to tachycardia), PERC rule - 0 points.

0 s

V

Fig. 3. CT pulmonary angiography

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However, a decision was made to determine the level of D-dimer, which significantly exceeded normal values (4781 FEO/ml). A computed tomo-graphic pulmonary angiography was performed (Fig. 3). It revealed left-sided pulmonary embolism with parietal thrombi of subsegmental arteries of the lower lobe of the left lung and pulmonary infarctions in S 5, 6, 9 of the left lung. Thus a diagnosis of PE was confirmed. Ultrasonography found no signs of DVT of lower limbs.

Patient was prescribed 30 mg of rivaroxaban per day with positive clinical effect. Provided that this episode of PE was recognised as unprovoked the patient was tested for thrombophilia. The following mutations were detected: heterozygous carriage of folate cycle mutations (MTRR 66, MTHFR1298, MTHFR 677, MTR 2756), factor XIII F13A1 mutation (heterozygous carriage), platelet glycoprotein ip GP1BA gene (heterozygous carriage 1), PAI-1 (heterozygous carriage 1). Markers of antiphospholipid syndrome have not been found. Given that the patient was on anticoagulant therapy, activity of antithrombin and levels of proteins C and S were not determined.

Despite the fact that all of the detected mutations themselves are not considered to increase the risk of

venous thrombosis, it is likely that their combination has a similar effect.

CONCLUSIONS

1. Nowadays, the health status of the young able to work population is often poor due to increasing prevalence of obesity, smoking and sedentary lifestyle, which makes them prone to developing PE. Thus, testing for thrombophilia in young patients with unprovoked PE is reasonable and feasible approach.

2. On the one hand, this is a way to inform the patient about the real risk of a repeated episode of thrombosis, which in the case of unprovoked pulmonary embolism occurs in 50% during the next 5 years, and thus to improve compliance when developing a thromboprophylaxis strategy. On the other hand, further accumulation and analysis of data on the totality of genetic risk factors for thrombosis will expand our understanding of this issue and in the future will allow us to better diagnose and treat this condition.

Conflict of interests. The authors declare no conflict of interest.

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СПИСОК Л1ТЕРАТУРИ

1. Clinical guidelines for testing for heritable thrombophilia / T. Baglin et al. Br. Journal of Haematology. 2010. P. 209-220. Epub 2010 Jan 28. PMID: 20128794.

DOI: https://doi.org/10.1111/j.1365-2141.2009.08022.x

2. Connors J. M. Thrombophilia Testing and Venous Thrombosis. N Engl J Med. 2017. 21. Sep. (Vol. 377, No. 12). P. 1177-1187. PMID: 28930509. DOI: https://doi.org/10.1056/NEJMra1700365

3. Guidance for the evaluation and treatment of hereditary and acquired thrombophilia / S. M. Stevens et al. J Thromb Thrombolysis. 2016. Vol. 41, No. 1. P. 154164. PMID: 26780744; PMCID: PMC4715840.

DOI: https://doi.org/10.1007/s11239-015-1316-1

4. Guidance for the treatment and prevention of obstetric-associated venous thromboembolism / S. M. Bates et al. J Thromb Thrombolysis. 2016. Vol. 41, No. 1. P. 92-128. PMID: 26780741; PMCID: PMC4715853. DOI: https://doi.org/10.1007/s11239-015-1309-0

5. Kireyeva T. V., Basina B. O., Kravchenko N. K. Pneumonia misdiagnosis. Are we loosing time? The Pharma Innovation Journal. 2019. Vol. 8, No. 5. P. 92-94.

6. Maynard G., Jenkins I. H., Merli G. J. VTE Prevention Guidelines for Inpatients. J. Hosp. Med. 2013. Vol. 10. P. 582-588. Epub. 2013 Aug 27. PMID: 23983041. DOI: https://doi.org/10.1002/jhm.2071

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8. Momot A. The problem of thrombophilia in clinical practice. Rus. Journal of Children Hematology and Oncology. 2015. Vol. 2. P. 36-48. DOI: https://doi.org/10.17650/2311-1267-2015-1-36-48

9. Rana S. Acute pulmonary embolism in young: Case reports. J Assoc Chest Physicians. 2017. Vol. 5. P. 46-50. DOI: https://doi.org/10.4103/2320-8775.196657

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DOI: https://doi.org/10.1183/13993003.01647-2019

Стаття надшшла до редакцп 09.12.2020

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