{"id":2025,"date":"2020-05-05T21:44:42","date_gmt":"2020-05-05T19:44:42","guid":{"rendered":"https:\/\/www.newslab.sk\/epidemiologicke-charakteristiky-pacientov-s-diabetom-mellitom-a-diabetickou-retinopatiou-na-slovensku-vysledky-zo-studie-diaret-sk\/"},"modified":"2020-05-06T09:39:41","modified_gmt":"2020-05-06T07:39:41","slug":"epidemiological-characteristics-of-patients-with-diabetic-retinopathy-in-slovakia-results-from-the-diaret-sk-study","status":"publish","type":"post","link":"https:\/\/www.newslab.sk\/en\/epidemiological-characteristics-of-patients-with-diabetic-retinopathy-in-slovakia-results-from-the-diaret-sk-study\/","title":{"rendered":"Epidemiological characteristics of patients with diabetic retinopathy in Slovakia: results from the DIARET SK study"},"content":{"rendered":"<p><span style=\"color: #ff0000;\"><strong>*<\/strong><strong>All tables, charts, graphs and pictures that are featured in this article can be found in the .pdf attachment at the end of the paper.<\/strong><\/span><\/p>\n<p>&nbsp;<\/p>\n<p><strong>\u00davod<\/strong><\/p>\n<p>Diabetes mellitus (DM) je jedn\u00fdm z najv\u00e4\u010d\u0161\u00edch zdravotn\u00fdch probl\u00e9mov 21. storo\u010dia. Pod\u013ea \u00fadajov Medzin\u00e1rodnej feder\u00e1cie diabetu (International Diabetes Federation) z roku 2017 m\u00e1 takmer 425 mili\u00f3nov \u013eud\u00ed vo veku 20 \u2013 79 rokov diabetes(1). Predpoklad\u00e1 sa, \u017ee do roku 2030 sa po\u010det pacientov s DM zv\u00fd\u0161i o 69 % v rozvojov\u00fdch a o 20 % v rozvinut\u00fdch krajin\u00e1ch(2). Diabetick\u00e1 retinopatia (DR) je hlavnou pr\u00ed\u010dinou straty zraku u dospel\u00fdch vo veku 20 \u2013 74 rokov(3). Viac ako tretina pacientov s DM m\u00e1 pr\u00edznaky DR a tretina z nich je postihnut\u00e1 diabetickou retinopatiou ohrozuj\u00facou zrak (VTDR), ktor\u00e1 je definovan\u00e1 ako z\u00e1va\u017en\u00e1 neproliferat\u00edvna DR alebo proliferat\u00edvna DR (PDR), alebo pr\u00edtomnos\u0165 diabetick\u00e9ho ed\u00e9mu makuly (DEM)(2). Trvanie diabetu a zl\u00e1 kontrola glyk\u00e9mie s\u00fa najd\u00f4le\u017eitej\u0161ie rizikov\u00e9 faktory spojen\u00e9 s v\u00fdvojom DR a v\u00e4\u010d\u0161inou chronick\u00fdch komplik\u00e1ci\u00ed s\u00favisiacich s diabetom. V\u00fdznamn\u00e9 klinick\u00e9 \u0161t\u00fadie, ako je \u201eThe Diabetes Control and Complications Trial\/Epidemiology of Diabetes Intervention and Complications (DCCT\/EDIC)\u201c, preuk\u00e1zali, \u017ee intenz\u00edvna lie\u010dba hyperglyk\u00e9mie \u00fa\u010dinne oneskoruje n\u00e1stup a spoma\u013euje progresiu komplik\u00e1ci\u00ed pri DM vr\u00e1tane DR(4). Dok\u00e1zalo sa, \u017ee okrem straty zraku prispievaj\u00fa DR a DEM k rozvoju \u010fal\u0161\u00edch komplik\u00e1ci\u00ed s\u00favisiacich s cukrovkou vr\u00e1tane nefropatie, perif\u00e9rnej neuropatie a kardiovaskul\u00e1rnych pr\u00edhod(5,6). V tejto pr\u00e1ci uv\u00e1dzame v\u00fdsledky \u0161t\u00fadie DIARET SK (Prevalencia <strong>DIA<\/strong>betickej <strong>RET<\/strong>inopatie a dopad genetick\u00fdch faktorov na vznik diabetickej retinopatie u pacientov s DM 1. a 2. typu na SlovensKu), ktorej cie\u013eom bolo zisti\u0165 epidemiologick\u00e9 a rizikov\u00e9 faktory pacientov s DM a DR.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>Materi\u00e1l a met\u00f3dy<\/strong><\/p>\n<p>DIARET SK bol epidemiologick\u00fd, multicentrick\u00fd prieskum u dospel\u00fdch pacientov (vo veku \u2265 18 rokov) s DM 1. a 2. typu, ktor\u00ed sp\u013a\u0148ali krit\u00e9ri\u00e1 na zaradenie a podp\u00edsali formul\u00e1r informovan\u00e9ho s\u00fahlasu s epidemiologick\u00fdm v\u00fdskumom. Ka\u017ed\u00fd zaraden\u00fd pacient absolvoval vy\u0161etrenie oboch o\u010d\u00ed aj u oftalmol\u00f3ga. Pacientom bol pridelen\u00fd unik\u00e1tny identifika\u010dn\u00fd k\u00f3d, aby sa zachovala anonymita, a identitu pacienta poznal iba o\u0161etruj\u00faci lek\u00e1r. \u00dadaje sa zbierali u 51 diabetol\u00f3gov a 47 oftalmol\u00f3gov v obdob\u00ed febru\u00e1r a\u017e december 2015. Zara\u010fovanie pacientov prebiehalo po\u010das n\u00e1v\u0161tev u diabetol\u00f3gov, pri ktor\u00fdch im boli vy\u0161etren\u00e9 potrebn\u00e9 parametre a tie boli elektronicky zaznamenan\u00e9 spolu s retrospekt\u00edvnymi anamnestick\u00fdmi \u00fadajmi. Aby sa zabezpe\u010dil nezaujat\u00fd v\u00fdber, pacienti boli vyberan\u00ed ka\u017ed\u00fd de\u0148 skr\u00edningu pod\u013ea vopred \u0161pecifikovan\u00e9ho poradia. Zahrnut\u00ed boli v\u0161etci pacienti s DM (1. aj 2. typu) bez oh\u013eadu na trvanie DM a bez oh\u013eadu na o\u010dn\u00e9 komplik\u00e1cie v pacientovej anamn\u00e9ze alebo pri vy\u0161etren\u00ed diabetol\u00f3gom. Pacienti boli vyraden\u00ed, ak mali 1) &lt; 18 rokov, 2) gesta\u010dn\u00fd diabetes alebo sekund\u00e1rny \u2013 indukovan\u00fd diabetes, 3) diabetick\u00fa ketoacid\u00f3zu alebo hyperosmol\u00e1rnu k\u00f3mu a 4) zneu\u017e\u00edvali alkohol alebo mali ak\u00fatnu intoxik\u00e1ciu alkoholom.<\/p>\n<p>\u0160tatistick\u00e1 anal\u00fdza: Ak\u00e9ko\u013evek zaujatie bolo eliminovan\u00e9 pou\u017eit\u00edm vopred \u0161pecifikovan\u00e9ho kv\u00e1zi n\u00e1hodn\u00e9ho procesu v\u00fdberu pacientov. V\u010faka vy\u0161\u0161iemu po\u010dtu pacientov sa o\u010dak\u00e1vali najpresnej\u0161ie v\u00fdsledky v zmysle \u0161tatistickej chyby vr\u00e1tane celkovej prevalencie a identifik\u00e1cie rizikov\u00fdch faktorov prispievaj\u00facich k vzniku DR. Prim\u00e1rne cie\u013eov\u00e9 v\u00fdsledky s\u00fa uv\u00e1dzan\u00e9 Wilsonov\u00fdm sk\u00f3re 95 % intervalu spo\u013eahlivosti (IS). Anal\u00fdza vplyvu rizikov\u00fdch faktorov na prevalenciu DR a DEM sa realizovala po- mocou multivaria\u010dnej logistickej regresie. Miera ch\u00fdbaj\u00facich hodn\u00f4t bola v\u0161eobecne n\u00edzka. Nedop\u013a\u0148ali sa ch\u00fdbaj\u00face d\u00e1ta. V anal\u00fdzach korel\u00e1ci\u00ed alebo logistick\u00fdch regresi\u00ed boli pou\u017eit\u00e9 v\u0161etky d\u00e1ta s dostupn\u00fdmi v\u00fdsledkami. Charakteristiky pacienta boli opisovan\u00e9 \u0161tandardn\u00fdmi met\u00f3dami deskript\u00edvnej \u0161tatistiky \u2013 celkov\u00fd po\u010det pacientov (N), percentu\u00e1lny podiel (%), prie- mer, medi\u00e1n, minimum, maximum, \u0161tandardn\u00e1 odch\u00fdlka (SD).<\/p>\n<p>&nbsp;<\/p>\n<h4>V\u00fdsledky<\/h4>\n<p>Kone\u010dn\u00fd s\u00fabor d\u00e1t obsahoval \u00fadaje od 4 014 pacientov. Pomocou kv\u00e1zi n\u00e1hodn\u00e9ho pr\u00edstupu bolo zaraden\u00fdch 3 700 pacientov (DM 2. typu = 3 405, DM 1. typu = 295), 16 (DM 2. typu = 15, DM 1. typu = 1) bolo zaraden\u00fdch v skupine vo- pred \u0161pecifikovanej s trvan\u00edm DM &lt; 5 rokov s hist\u00f3riou DR a 298 (DM 2. typu = 204, DM 1. typu = 94) pacientov s trvan\u00edm DM \u2265 20 rokov. V\u00fdsledky s\u00fa uv\u00e1dzan\u00e9 zvl\u00e1\u0161\u0165 pod\u013ea typu DM.<\/p>\n<p>Podiel \u017eien bol podobn\u00fd v oboch skupin\u00e1ch s DM 2. aj\u00a0 1. typu (1 806 [53 %) vs 154 [52,2 %], v uvedenom porad\u00ed). Priemern\u00fd vek (SD) v \u010dase diagnostikovania DM bol 53,4 (9,5) roka u pacientov s DM 2. typu a 27,6 (12,9) roka s DM 1. typu. Priemern\u00fd vek (SD) pacientov bol 60,9 (9,5) roka u pacientov s DM 2. typu a 37,9 (12,1) roka u pacientov s DM 2. typu. V\u00e4\u010d\u0161ina pacientov v skupine s DM 2. typu bola vo veku medzi 50 \u2013 70 rokov, zatia\u013e \u010do v skupine s DM 1. typu boli do 45 rokov <strong><em>(obr\u00e1zok 1 A a B)<\/em>.<\/strong><\/p>\n<p>Priemer (SD) trvania DM 2. typu bol 7,5 (5,2) roka a DM 1. typu 10,3 (6,9) roka. Trvanie ochorenia DM 2. typu u v\u00e4\u010d- \u0161iny (69,4 %) pacientov bolo &lt; 10 rokov a viac ako \u2265 20 rokov iba u 40 (1,2 %) pacientov. Zo v\u0161etk\u00fdch pacientov s DM 2. typu malo 46,8 % trvanie ochorenia &lt; 10 rokov a iba 5,4 % \u2265 20 rokov. Trvanie DM 2. a 1. typu kategorizovan\u00e9 pod\u013ea rokov trvania je zobrazen\u00e9 na <strong><em>obr\u00e1zku 2 C a D<\/em><\/strong>.<\/p>\n<p>Priemer (SD) HbA1c (% DCCT) bol 7,5 (1,4) u pacientov s DM 2. typu a 8,5 (1,6) u pacientov s DM 1. typu. Hladiny HbA1c sa u v\u00e4\u010d\u0161iny (72,6 %) pacientov s DM 2. typu pohybovali medzi 6 % \u2013 8,5 %, zatia\u013e \u010do u v\u00e4\u010d\u0161iny (63,7 %) pacientov s DM 1. typu sa hladiny HbA1c pohybovali medzi 6,5 % \u2013 9 %. Celkovo 55,2 % pacientov s DM 2. typu a 81,8 % pacientov s DM 1. typu malo hladiny HbA1c nad norm\u00e1lnym rozp\u00e4t\u00edm (&lt; 7 %)(7). Pri DM 2. typu mali 2 % pacientov hladiny HbA1c &gt; 11, zatia\u013e \u010do pri DM 1. typu malo hladiny HbA1c &gt; 11 5,8 % pacientov <strong><em>(obr\u00e1zok 3 E a F)<\/em><\/strong>.<\/p>\n<p>DCCT, \u0161t\u00fadia kontroly a komplik\u00e1ci\u00ed diabetu; HbA1c, glykovan\u00fd hemoglob\u00edn<\/p>\n<p>Prevalencia DR bola vy\u0161\u0161ia u pacientov s DM 2. a 1. typu s trvan\u00edm ochorenia \u2265 20 rokov v porovnan\u00ed s trvan\u00edm DM &lt; 20 rokov <strong><em>(tabu\u013eka 1)<\/em><\/strong>.<\/p>\n<h4><\/h4>\n<h4>Diskusia<\/h4>\n<p>\u0160t\u00fadia DIARET SK bola prv\u00e1 a zatia\u013e jedin\u00e1 na Slovensku, v ktorej sa hodnotili epidemiologick\u00e9 charakteristiky pacientov s DM a DR a ich vplyv na vznik DR a DEM. Prevalencia DM st\u00fapa s rast\u00facim vekom(8) a sp\u00f4sobuje komplik\u00e1cie s\u00favisiace s DR. DR je k\u013e\u00fa\u010dov\u00fdm indik\u00e1torom mikrovaskul\u00e1rnych komplik\u00e1ci\u00ed s\u00favisiacich s DM. V tejto \u0161t\u00fadii bol priemern\u00fd vek pacientov s DM 2. typu vy\u0161\u0161\u00ed ako u pacientov s DM 1. typu a na\u0161e v\u00fdsledky s\u00fa podobn\u00e9, ako v\u00fdsledky hl\u00e1sen\u00e9 z ned\u00e1vno publikovanej d\u00e1nskej \u0161t\u00fadie(9). Sk\u00famanie rizikov\u00fdch faktorov tie\u017e odhalilo zauj\u00edmav\u00e9 \u00favahy v klinickej praxi aj vo v\u00fdskume. Hyperglyk\u00e9mia zost\u00e1va najd\u00f4le\u017eitej\u0161\u00edm modifikovate\u013en\u00fdm rizikov\u00fdm faktorom DR. HbA1c predstavuje chronick\u00fa koncentr\u00e1ciu gluk\u00f3zy v krvi a pou\u017e\u00edva sa ako marker na predpovedanie bud\u00facich komplik\u00e1ci\u00ed s\u00favisiacich s DM a ako kritick\u00fd parameter na hodnotenie vplyvu ochorenia(10). Na zistenie efektu zn\u00ed\u017een\u00fdch hlad\u00edn gluk\u00f3zy v krvi na mikrovaskul\u00e1rne komplik\u00e1cie u pacientov s DM 2. typu a 1. typu sa realizovalo nieko\u013eko klinick\u00fdch \u0161t\u00fadi\u00ed. V\u00fdsledky \u0161t\u00fadi\u00ed nazna\u010dili, \u017ee chronick\u00e9 zn\u00ed\u017eenie hlad\u00edn gluk\u00f3zy v krvi n\u00e1sledne zn\u00ed\u017eilo riziko DR(11-14). V\u00fdsledky zo \u0161t\u00fadie kontroly a komplik\u00e1ci\u00ed diabetu (Diabetes Control and Complications Trial (DCCT)) v USA a Kanade pre DM 1. typu(11) a z prospekt\u00edvnej \u0161t\u00fadie DM v Spojenom kr\u00e1\u013eovstve (the United Kingdom Prospective Diabetes Study (UKPDS)) pre DM 2. typu(12) uk\u00e1zali ve\u013emi v\u00fdznamn\u00e9 zn\u00ed\u017eenia (DCCT, p &lt; 0,001; UKPDS, p = 0,009) incidencie a progresie DR u pacientov randomizovan\u00fdch na pr\u00edsnu kontrolu gluk\u00f3zy v krvi (HbA1c &lt; 7 %). Na druhej strane v\u00fdsledky zo \u0161t\u00fadi\u00ed ADVANCE a ACCORD uk\u00e1zali, \u017ee agres\u00edvna kontrola glyk\u00e9mie (&lt; 6,5 %) v\u00fdznamne nezn\u00ed\u017eila riziko retinopatie(15,16).<\/p>\n<p>V \u0161t\u00fadii DIARET, bez oh\u013eadu na typ DM, mala v\u00e4\u010d\u0161ina pacientov priemern\u00e9 hladiny HbA1c nad norm\u00e1lnym rozp\u00e4t\u00edm (&gt; 7 %). Priemern\u00e9 hladiny HbA1c boli vy\u0161\u0161ie u pacientov\u00a0 s DM 1. typu v porovnan\u00ed s pacientmi 2. typu, \u010do m\u00f4\u017ee by\u0165 jedn\u00fdm z d\u00f4vodov vy\u0161\u0161ej prevalencie DR u pacientov s DM 1. typu v \u0161t\u00fadii DIARET Tieto v\u00fdsledky zo \u0161t\u00fadie DIARET SK s\u00fa podobn\u00e9 ako v\u00fdsledky hl\u00e1sen\u00e9 zo \u0161panielskej popul\u00e1cie (priemer [SD]: 7,38 \u00b1 1,29 % pre DM 2. typu a 8,38 \u00b1 1,16 % pre DM 1. typu). Autori vy\u0161\u0161ie hodnoty ak\u00fdchko\u013evek DR pri DM 1. typu vysvet\u013euj\u00fa dvoma r\u00f4znymi pr\u00ed\u010dinami: (i) dlh\u0161ie trvanie DM (13,63 \u00b1 8,42 roka u pacientov s DM 1. typu v porovnan\u00ed s 8,25 \u00b1 6,1 roka u pacientov s DM 2. typu) a (ii) zl\u00e1 metabolick\u00e1 kontrola meran\u00e1 pomocou HbA1c (8,38 \u00b1 1,16 % u pacientov s DM 1. typu v porovnan\u00ed so 7,38 \u00b1 1,29 % u pacientov s DM 2. typu)(19). V liverpoolskej \u0161t\u00fadii bol medi\u00e1n trvania DM pri 2. type 3,2 roka a pri DM 1. typu 12,8 roka, vo waleskej \u0161t\u00fadii 5,3 roka a 16,7 roka v uvedenom porad\u00ed a v d\u00e1nskej \u0161t\u00fadii 8 rokov a 19 rokov v uvedenom porad\u00ed(17-19). V na\u0161ej \u0161t\u00fadii bol medi\u00e1n trvania DM 7 rokov u pacientov s DM 2. typu a 10 rokov u pacientov s DM 1. typu. V \u0161t\u00fadii DIARET SK v\u00e4\u010d\u0161ina pacientov s DM 2. typu (69,4 %) ud\u00e1vala trvanie ochorenia &lt; 10 rokov a iba 30,6 % pacientov s DM 1. typu a 53,2 % s DM typu &gt; 10 rokov. To m\u00f4\u017ee by\u0165 jeden z d\u00f4vodov vy\u0161\u0161ej prevalencie DR medzi pacientmi s DM 1. typu v tejto \u0161t\u00fadii podobne, ako to bolo pozorovan\u00e9 v predch\u00e1dzaj\u00facich publikovan\u00fdch \u0161t\u00fadi\u00e1ch(17-19). T\u00e1to epidemiologick\u00e1 \u0161t\u00fadia na slovenskej popul\u00e1cii potvrdzuje v\u00fdsledky predch\u00e1dzaj\u00facich \u0161t\u00fadi\u00ed v in\u00fdch popul\u00e1ci\u00e1ch, \u017ee glykemick\u00e1 expoz\u00edcia (trvanie p\u00f4sobenia DM a HbA1c) je prevl\u00e1da- j\u00facim faktorom pri vzniku DR. V\u010dasn\u00e1 detekcia, dobr\u00e1 kontrola HbA1c a r\u00fdchla lie\u010dba umo\u017e\u0148uj\u00fa prevenciu zrakov\u00e9ho po\u0161kodenia s\u00favisiaceho s DM, lep\u0161\u00ed mana\u017ement t\u00fdchto pacientov a zn\u00ed\u017eenie z\u00e1\u0165a\u017ee lie\u010dbou. Pacienti s DM si vy\u017eaduj\u00fa pravideln\u00e9 sledovanie lek\u00e1rmi prim\u00e1rnej starostlivosti, aby optimalizovali svoj glykemick\u00fd index a aby sa zabr\u00e1nilo v\u00fdvoju a progresii DR a \u010fal\u0161\u00edch komplik\u00e1ci\u00ed s\u00favisiacich s DM. \u00dadaje zo \u0161t\u00fadie DIARET SK poskytuj\u00fa z\u00e1klad na porovnanie slovensk\u00fdch epidemiologick\u00fdch \u00fadajov so \u0161t\u00fadiami z in\u00fdch kraj\u00edn, poskytuj\u00fa poh\u013ead na mana\u017ement a lep\u0161ie porozumenie tohto ochorenia ohrozuj\u00faceho zrak. DIARET SK je prv\u00e1 rozsiahla, dobre kontrolovan\u00e1 epidemiologick\u00e1 \u0161t\u00fadia, ktor\u00e1 hodnotila epidemiologick\u00e9 charakteristiky pacientov s DM a DR. Hlavnou silnou str\u00e1nkou tejto \u0161t\u00fadie je ve\u013ek\u00e1 vzorka pacientov. Pokia\u013e je n\u00e1m zn\u00e1me, zatia\u013e nebola publikovan\u00e1 \u017eiadna in\u00e1 epidemiologick\u00e1 \u0161t\u00fadia s tak\u00fdm vysok\u00fdm po\u010dtom pacientov.<\/p>\n<p>&nbsp;<\/p>\n<p><strong><em>Po\u010fakovanie: <\/em><\/strong><em>Tento <\/em><em>\u010dl\u00e1nok vznikol v\u010faka podpore v r\u00e1mci OP V\u00fdskum a v\u00fdvoj pre projekt: Centrum v\u00fdskumu z\u00e1va\u017en\u00fdch ochoren\u00ed a ich komplik\u00e1ci\u00ed, ITMS 26240120038, spolufinancovan\u00fd zo zdrojov Eur\u00f3pskeho fondu region\u00e1lneho rozvoja.<\/em><\/p>\n<p><em>MUDr.<\/em> <em>Marta Ondrejkov\u00e1, PhD.: Potvrdzujem, \u017ee som dostala finan\u010dn\u00fa podporu od farmaceutick\u00fdch spolo\u010dnost\u00ed Novartis a Bayer ako \u010dlenka Advisory Boardu a investig\u00e1torka v klinick\u00fdch \u0161t\u00fadi\u00e1ch.<\/em><\/p>\n<p><em>MUDr.<\/em> <em>Monika Gajdo\u0161ov\u00e1: Spolupracujem s farmaceutick\u00fd- mi spolo\u010dnos\u0165ami Novartis, Bayer, Allergan a Zeiss ako konzultantka. Som \u010dlenka Advisory Boardu spolo\u010dnost\u00ed Novartis, Bayer, Allergan a hlavn\u00e1 sk\u00fa\u0161aj\u00faca vo viacer\u00fdch klinick\u00fdch \u0161t\u00fadi\u00e1ch.<\/em><\/p>\n<p><em>MUDr.<\/em> <em>Iveta Tvrd\u00e1 a MUDr. Jana Fabkov\u00e1: Potvrdzujeme, \u017ee sme zamestnankyne medic\u00ednskeho oddelenia spolo\u010dnosti Novartis Slovakia, s. r. o., \u017di\u017ekova 22B, Bratislava.<\/em><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p><strong>LITERAT\u00daRA<\/strong><\/p>\n<ol>\n<li>IDF DIABETES ATLAS \u2013 8TH dostupn\u00e9 na: http:\/\/www.dia- betesatlas.org\/across-the-globe.html (pr\u00edstup 29. okt\u00f3bra 2019).<\/li>\n<li>Yau JW, Rogers SL, Kawasaki R, et al. Global prevalence and major risk factors of diabetic retinopathy. Diabetes Care 2012; 35(3): 556-564.<\/li>\n<li>Cheung N, Mitchell P, Wong Diabetic retinopathy. Lancet 2010; 376(9735): 124-136.<\/li>\n<li>The Diabetes Control and Complications Trial (DCCT)\/Epidemiology of Diabetes Interventions and Complications (EDIC) Research Group. Effect of intensive diabetes therapy on the progression of diabetic retinop- athy in patients with type 1 diabetes: 18 years of follow-up in the DCCT\/ EDIC. Diabetes 2015; 64(2): 631-642.<\/li>\n<li>Hagg S, Thorn LM, Putaala J, et Incidence of stroke according to presence of diabetic nephropathy and severe diabetic retinopathy in pa- tients with type 1 diabetes. Diabetes Care 2013; 36(12): 4140-4146.<\/li>\n<li>Mottl AK, Pajewski N, Fonseca V, et The degree of retinopathy is equally predictive for renal and macrovascular outcomes in the ACCORD Trial. J Diabetes Complications 2014; 28(6): 874-879.<\/li>\n<li>Inzucchi SE, Bergenstal RM, Buse JB, et al. Management of hyperglycemia in type 2 diabetes: a patient-centered approach: position statement of the American Diabetes Association (ADA) and the European As- sociation for the Study of Diabetes (EASD). Diabetes Care 2012; 35(6): 1364-1379.<\/li>\n<li>Wild S, Roglic G, Green A, et al. Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care 2004; 27(5): 1047-1053.<\/li>\n<li>Larsen MB, Henriksen JE, Grauslund J, et Prevalence and risk factors for diabetic retinopathy in 17 152 patients from the island of Funen, Denmark. Acta Ophthalmologica 2017; 95(8): 778-786.<\/li>\n<li>Selvin E, Steffes MW, Zhu H, et al. Glycated hemoglobin, diabetes, and cardiovascular risk in nondiabetic N Engl J Med 2010; 362(9): 800-811.<\/li>\n<li>Diabetic retinopathy after two years of intensified insulin treatment. Follow-up of the Kroc Collaborative The Kroc Collaborative Study Group. JAMA 1988; 260(1): 37-41.<\/li>\n<li>Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group. Lancet 1998; 352(9131): 837-853.<\/li>\n<li>Dahl-Jorgensen K, Brinchmann-Hansen O, Hanssen KF, et al. Effect of near normoglycaemia for two years on progression of early diabetic retinopathy, nephropathy, and neuropathy: the Oslo Br Med J (Clin Res Ed) 1986; 293(6556): 1195-1199.<\/li>\n<li>Nathan DM, Genuth S, Lachin J, et The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Engl J Med 1993; 329(14): 977-986.<\/li>\n<li>Gerstein HC, Miller ME, Byington RP, et al. Effects of intensive glucose lowering in type 2 N Engl J Med. 2008; 358(24): 2545-259.<\/li>\n<li>Patel A, MacMahon S, Chalmers J, et Intensive blood glucose control and vascular outcomes in patients with type 2 diabetes. N Engl J Med 2008; 358(24): 2560-2572.<\/li>\n<li>Younis N, Broadbent DM, Harding SP, et Prevalence of diabetic eye disease in patients entering a systematic primary care-based eye screening programme. Diabet Med 2002; 19(12):1014-1021.<\/li>\n<li>Thomas RL, Dunstan FD, Luzio SD, Chowdhury SR, North RV, Hale SL, et Prevalence of diabetic retinopathy within a national diabetic retinopathy screening service. Br J Ophthalmol 2015; 99(1): 64-68.<\/li>\n<li>Romero-Aroca P, Navarro-Gil R, Valls-Mateu A, et Differences in incidence of diabetic retinopathy between type 1 and 2 diabetes mellitus: a nine-year follow-up study. Br J Ophthalmol 2017; 101(10): 1346-1351.<\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>*All tables, charts, graphs and pictures that are featured in this article can be found in the .pdf attachment at the end of the paper. &nbsp; \u00davod Diabetes mellitus (DM) je jedn\u00fdm z najv\u00e4\u010d\u0161\u00edch zdravotn\u00fdch probl\u00e9mov 21. storo\u010dia. Pod\u013ea \u00fadajov Medzin\u00e1rodnej feder\u00e1cie diabetu (International Diabetes Federation) z roku 2017 m\u00e1 takmer 425 mili\u00f3nov \u013eud\u00ed vo<\/p>\n","protected":false},"author":7,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_mi_skip_tracking":false,"footnotes":""},"categories":[287],"tags":[1510,735,1509,1506,1507],"class_list":["post-2025","post","type-post","status-publish","format-standard","hentry","category-uncategorized","tag-diabetic-macular-oedema","tag-diabetic-retinopathy","tag-gly-cated-hemoglobin","tag-type-1-diabetes-mellitus","tag-type-2-diabetes-mellitus","typ_clanku-original-work"],"acf":{"abstrakt":"<p>Diabetic retinopathy (DR) is the major cause of blindness in patients with diabetes mellitus (DM). DIARET SK is the first epidemiological and multi-centre study in Slovakia aimed at evaluating the epidemiological character- istics in Slovak patients with type 1 and type 2 DM and DR. The epidemiological and multicenter survey includ- ed 4078 adult patients (\u226518 years of age) from 51 diabetologists and 47 ophthalmologists. The study enrolled 3700 patients (type 1 DM = 295, type 2 DM = 3405). The mean (SD) glycated hemoglobin (HbA1c) was 7.5(1,4) in type 2 DM patients and 8.5(1,6) in type 1 DM patients. The mean duration of type 2 DM was shorter compared to type 1 DM (7.5 [5.2] vs 10.3 [6.9] years). The most frequent factors contributing to the development of DR and DEM in Slovak patients were disease duration and higher HbA1c.<\/p>\n<p><strong>Keywords: <\/strong>diabetic retinopathy, type 1 diabetes mellitus, type 2 diabetes mellitus, diabetic macular oedema, gly- cated hemoglobin<\/p>\n","casopis":[{"ID":1893,"post_author":"7","post_date":"2020-05-05 11:32:54","post_date_gmt":"2020-05-05 09:32:54","post_content":"<ul>\r\n \t<li>Identification of metabolic pathways in pathogenesis of diabetic retinopathy using exome sequencing \u2013 a pilot study<\/li>\r\n \t<li>Anti-tumour effects of vitamin D<\/li>\r\n \t<li>Molecular detection methods of mutations in the kinase domain of fusion gene bcr-abl1 in patients with chronic myelocyte leukemia<\/li>\r\n \t<li>The case report of toxoplasmic meningoencephalitis with fatal outcome in HIV patient<\/li>\r\n \t<li>Carcinosarcoma-like endometrioid carcinoma of the uterus: case report of rare non-high-grade tumor<\/li>\r\n<\/ul>","post_title":"newsLab","post_excerpt":"","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"newslab-4","to_ping":"","pinged":"","post_modified":"2020-05-05 15:13:41","post_modified_gmt":"2020-05-05 13:13:41","post_content_filtered":"","post_parent":0,"guid":"https:\/\/www.newslab.sk\/?post_type=casopis&#038;p=1893","menu_order":0,"post_type":"casopis","post_mime_type":"","comment_count":"0","filter":"raw"}],"strana":"9-13","upload_clanok":{"ID":2023,"id":2023,"title":"NEWSLAB_1-2020_Ondrejkov\u00e1","filename":"NEWSLAB_1-2020_Ondrejkov\u00e1.pdf","filesize":287543,"url":"https:\/\/www.newslab.sk\/wp-content\/uploads\/2020\/05\/NEWSLAB_1-2020_Ondrejkov\u00e1.pdf","link":"https:\/\/www.newslab.sk\/en\/epidemiological-characteristics-of-patients-with-diabetic-retinopathy-in-slovakia-results-from-the-diaret-sk-study\/newslab_1-2020_ondrejkova-3\/","alt":"","author":"7","description":"","caption":"","name":"newslab_1-2020_ondrejkova-3","status":"inherit","uploaded_to":2025,"date":"2020-05-05 19:34:19","modified":"2020-05-05 19:34:19","menu_order":0,"mime_type":"application\/pdf","type":"application","subtype":"pdf","icon":"https:\/\/www.newslab.sk\/wp-includes\/images\/media\/document.png"}},"_links":{"self":[{"href":"https:\/\/www.newslab.sk\/en\/wp-json\/wp\/v2\/posts\/2025","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.newslab.sk\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.newslab.sk\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.newslab.sk\/en\/wp-json\/wp\/v2\/users\/7"}],"replies":[{"embeddable":true,"href":"https:\/\/www.newslab.sk\/en\/wp-json\/wp\/v2\/comments?post=2025"}],"version-history":[{"count":0,"href":"https:\/\/www.newslab.sk\/en\/wp-json\/wp\/v2\/posts\/2025\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.newslab.sk\/en\/wp-json\/wp\/v2\/media?parent=2025"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.newslab.sk\/en\/wp-json\/wp\/v2\/categories?post=2025"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.newslab.sk\/en\/wp-json\/wp\/v2\/tags?post=2025"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}