TIGHT BLOOD-PRESSURE CONTROL AND RISK OF MACROVASCULAR AND MICROVASCULAR COMPLICATIONS IN TYPE-2 DIABETES - UKPDS 38

Authors
STEARNE MR PALMER SL HAMMERSLEY MS FRANKLIN SL SPIVEY RS LEVY JC TIDY CR BELL NJ STEEMSON J BARROW BA COSTER R WARING K NOLAN J TRUSCOTT E WALRAVENS N COOK L LAMPARD H MERLE C PARKER P MCVITTIE J DRAISEY I MURCHISON LE BRUNT AHE WILLIAMS MJ PEARSON DW PETRIE XMP LEAN MEJ WALMSLEY D LYALL MJ CHRISTIE E CHURCH J THOMSON E FARROW A STOWERS JM STOWERS M MCHARDY K PATTERSON N WRIGHT AD LEVI NA SHEARER ACI THOMPSON RJW TAYLOR G RAYTON S BRADBURY M GLOVER A SMYTHOSBOURNE A PARKES C GRAHAM J ENGLAND P GYDE S EAGLE C CHAKRABARTI B SMITH J SHERWELL J KOHNER EM DORNHURST A DODDRIDGE MC DUMSKYJ M WALJI S SHARP P SLEIGHTHOLM M VANTERPOOL G ROSE C FROST G ROSEBLADE M ELLIOTT S FORRESTER S FOSTER M MYERS K CHAPMAN R HAYES JR HENRY RW FEATHERSTON MS ARCHBOLD GPR COPELAND M HARPER R RICHARDSON I MARTIN S FOSTER M DAVISON HA HADDEN DR KENNEDY L ATKINSON AB CULBERT AM HEGAN C TENNET H WEBB N ROBINSON I HOLMES J FOSTER M BELL PM MCCANCE DR RUTHERFORD J NESBITT S SPATHIS AS HYER S NANSON ME JAMES LM TYRELL JM DAVIS C STRUGNELL P BOOTH M PETRIE H CLARK D RICE B HULLAND S BARRON JL YUDKIN JS GOULD BJ SINGER J BADENOCK A WALJI S ECKERT M ALIBHAI K MARRIOT E COX C PRICE R FERNANDEZ M RYLE A CLARKE S WALLACE G MEHMED E MACFARLANE S GREENWOOD RH WILSON J DENHOLM MJ TEMPLE RC WHITFIELD K JOHNSON F MUNROE C GORICK S DUCKWORTH E FLATMAN M RAINBOW S BORTHWICK LJ WHEATCROFT DJ SEAMAN RJ CHRISTIE RA WHEATCROFT W MUSK P WHITE J MCDOUGAL S BOND M RANIGA P NEWTON RW JUNG RT ROXBURGH C KILGALLON B DICK L FOSTER M WAUGH N KILBY S ELLINGFORD A BURNS J FOX CV HOLLOWAY MC COGHILL HM HEIN N FOX A COWAN W RICHARD M QUESTED K EVANS SJ PAISEY RB BROWN NPR TUCKER AJ PAISEY R GARRETT F HOGG J PARK P WILLIAMS K HARVEY P WILCOCKS R MASON S FROST J WARREN C ROCKET P BOWER L ROLAND JM BROWN DJ YOUENS J STANTONKING K MUNGALL H BALL V MADDISON W DONNELLY D KING S GRIFFIN P SMITH S CHURCH S DUNN G WILSON A PALMER K BROWN PM HUMPHRISS D DAVIDSON AJM ROSE R ARMISTEAD L TOWNSEND S POON P PEACOCK IDA CULVERWELL NJC CHARLTON MH CONNOLLY BPS PEACOCK J BARRETT J WAIN J BEESTON W KING G HILL PG BOULTON AJM ROBERTSON AM KATOULIS V OLUKOGA A MCDONALD H KUMAR S ABOUAESHA F ABUAISHA B KNOWLES EA HIGGINS S BOOKER J SUNTER J BREISLIN K PARKER R RAVAL P CURWELL J DAVENPORT H SHAWCROSS G PREST A GREY J COLE H SEREVIRATNE C YOUNG RJ DORNAN TL CLYNE JR GIBSON M OCONNELL I WONG LM WILSON SJ WRIGHT KL WALLACE C MCDOWELL D BURDEN AC SELLEN EM GREGORY R ROSHAN M VAGHELA N BURDEN M SHERRIFF C CLARKE J GRENFELL J TOOKE JE MACLEOD K SEARNARK C RAMMELL M PYM C STOCKMAN J YEO C PIPER J LEIGHTON L GREEN E HOYLE M JONES K HUDSON A JAMES AJ SHORE A HIGHAM A MARTIN B
Citation
Mr. Stearne et al., TIGHT BLOOD-PRESSURE CONTROL AND RISK OF MACROVASCULAR AND MICROVASCULAR COMPLICATIONS IN TYPE-2 DIABETES - UKPDS 38, BMJ. British medical journal, 317(7160), 1998, pp. 703-713
Citations number
43
Categorie Soggetti
Medicine, General & Internal
ISSN journal
09598138
Volume
317
Issue
7160
Year of publication
1998
Pages
703 - 713
Database
ISI
SICI code
0959-8138(1998)317:7160<703:TBCARO>2.0.ZU;2-O
Abstract
Objective: To determine whether tight control of blood pressure preven ts macrovascular and microvascular complications in patients with type 2 diabetes. Design: Randomised controlled trial comparing tight contr ol of blood pressure aiming at a blood pressure of <150/85 mm Hg (with the use of an angiotensin converting enzyme inhibitor captopril or a beta blocker atenolol as main treatment) with less tight control aimin g at a blood pressure of <.180/105 mm Hg. Setting 20 hospital based cl inics in England, Scotland, and Northern Ireland. Subjects: 1148 hyper tensive patients with type 2 diabetes (mean age 56, mean blood pressur e at entry 160/94 mm Hg); 758 patients were allocated to tight control of blood pressure and 390 patients to less tight control with a media n follow up of 8.4 years. Main outcome measures: Predefined clinical e nd points, fatal and non-fatal, related to diabetes, deaths related to diabetes, and all cause mortality. Surrogate measures of microvascula r disease included urinary albumin excretion and retinal photography. Results: Mean blood pressure during follow up was significantly reduce d in the group assigned tight blood pressure control (144/82 mm Hg) co mpared with the group assigned to less tight control (154/87 mm Hg) (P < 0.0001). Reductions in risk in the group assigned to tight control c ompared with that assigned to less tight control were 24% in diabetes related end points (95% confidence interval 8% to 38%) (P= 0.0046), 32 % in deaths related to diabetes (6% to 51%) (P= 0.019), 44% in strokes (11% to 65%) (P= 0.013), and 37% in microvascular end points (11% to 56%) (P= 0.0092), predominantly owing to a reduced risk of retinal pho tocoagulation. There was a non-significant reduction in all cause mort ality. After nine years of follow up the group assigned to tight blood pressure control also had a 34% reduction in risk in the proportion o f patients with deterioration of retinopathy by two steps (99% confide nce interval 11% to 50%) (P= 0.0004) and a 47% reduced risk (7% to 70% ) (P = 0.004) of deterioration in visual acuity by three lines of the early treatment of diabetic retinopathy study (ETDRS) chart. After nin e years of follow up 29% of patients in the group assigned to tight co ntrol required three or more treatments to lower blood pressure to ach ieve target blood pressures. Conclusion: Tight blood pressure control in patients with hypertension and type 2 diabetes achieves a clinicall y important reduction in the risk of deaths related to diabetes, compl ications related to diabetes, progression of diabetic retinopathy, and deterioration in visual acuity.